Endocrine Abstracts

Previous issue | Volume 110 | ECEESPE2025

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

Prize Lectures
- Endocrinology Across the Life Course Award
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- The Geoffrey Harris Award Lecture
- - Learning from rare diseases: from corticotroph deficiency to corticotroph adenomas
    
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- Andrea Prader Award
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- Research Award
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- The European Journal of Endocrinology Award Lecture
- - MODY and Beyond: The Changing Face of Monogenic Diabetes
    
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- Outstanding Clinician Award & The International Outstanding Clinician Award
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- Clinical Endocrinology Journal Foundation Award Lecture
- - Tackling adrenocortical cancer: a clinician perspective
    
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- International Research Award and The Hormone Research in Paediatrics Prize
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- European Hormone Medal Award Lecture
- - Disorders of thyroid hormone action: insights from human genetics
    
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- ESPE Young Investigator Awards
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- Jens Sandahl Christiansen Awards
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  - Importance of gut microbiota for the effectiveness of weight loss - role of glucocorticoids
    
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- Henning Andersen Award Presentations
- - Association between premature ovarian insufficiency and biological aging: evidence from the UK Biobank and NHANES population-based surveys
    
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  - USP8 genotype is associated with recurrence risk in Cushing's disease: an international, retrospective, multicenter cohort study
    
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Plenary Lectures
- Plenary Lectures
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  - Thyroid Cancer Across the Lifespan: Similar yet Different
    
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  - Adverse effects of endocrine disrupting chemicals though life course
    
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  - Unlocking the secrets of exercise: A pathway to enhanced insulin sensitivity and metabolism in type 2 diabetes
    
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Symposia
- Symposia
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  - Transition for Prader Willi Syndrome
    
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  - A data-based campaign on reducing exposure to Endocrine Disruptors in mother-infant dyads: the Life Milch Project
    
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  - Management of bone fragilty and osteoporosis in children and adolescence
    
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  - Novel therapies in osteogenesis imperfecta
    
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  - Current Challenges and New Perspectives in Cyclic Cushing's Syndrome
    
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  - Population screening of early stage Type 1 diabetes
    
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  - Novel targets and sequential therapies in neuroendocrine neoplasms
    
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  - Molecular basis of short stature
    
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  - Intratumoral glucocorticoid secretion in adrenocortical carcinoma and its implication for CAR-T cell targeting
    
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  - Safety of GH replacement in adults with hypopituitarism
    
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  - Endocrine disruptors affect male reproductive disorders in fetal and early postnatal life
    
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  - The evolutionary pressure on humans and other mammals to be reproductively successful
    
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  - Calcium sensing receptor and its function in health and disease
    
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  - Recent advances in the diagnosis and management of Hypophosphatasia
    
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  - Molecular basis of Pseudohypoparthyroidism
    
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  - Regulation of HPT-axis in maternal-foetal health - Thyroid and Fertility
    
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  - International Diabetes Transition Recommendations- a joint initiative between ISPAD- ADA- EASD
    
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  - Recombinant antibody fragments as new modulators of gonadotropin receptor activity
    
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  - The long-term effects of duchenne muscular dystrophy and its treatment on bone strength
    
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  - Transition from boy to man - Puberty/testosterone
    
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  - Novel genetic causes for CHI
    
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  - What is new in CHI therapeutics - Alpelisib
    
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  - The relevance of Epigentics variability on Phenotype variation
    
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  - Senolytics and senomorphics: new treatments on the door?
    
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  - Genetic determinants of normal pubertal timing
    
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  - Definition of puberty onset in boys - secular changes?
    
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  - AMH as reproductive marker in healthy females and Turner syndrome patients from birth to adulthood
    
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  - The biochemical and clinical significance of 11-oxygenated androgens
    
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  - New therapeutic steroid sparing options for Congenital Adrenal Hyperplasia
    
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  - Novel approaches to glucocorticoid replacement
    
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  - Diabetes mellitus and Bone fragility: Pathophysiological aspects
    
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  - Sleep disturbances in patients with pituitary tumours
    
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  - Insufficient sleep in obesity: An eating jet lag
    
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  - Thyroid Hormone Resistance
    
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  - >50 years of neonatal screening - where do we stand?
    
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  - Germline variants in non-medullary thyroid cancer'
    
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  - Pregnancy following bariatric surgery
    
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  - Don't mess with my iodine! chemical-induced perturbation in synthesis and metabolism of thyroid hormone impairs brain development
    
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  - Neurodevelopmental effects of thyroid hormone system disruption - insights from the ATHENA project
    
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  - EDC targets of the thyroid hormone system - HTS and in vivo assays for identification of potential reference compounds'
    
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  - Genetic regulation of osteoarthritis pathogenesis
    
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  - Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome)
    
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  - The genetic spectrum of PA: from monogenic disorders to aldosterone dysregulation in hypertension
    
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  - Precision medicine in diabetes
    
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  - The impact of rare gene variants in common diabetes and obesity
    
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  - Central regulation of body weight
    
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  - Pharmacological treatment of obesity in adults and its impact on comorbidities
    
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  - Epigenetic memory of fat cells: the role in weight regain
    
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Debate Sessions
- Debate Sessions
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  - Metformin is not effective and safe during pregnancy in women with PCOS
    
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Meet The Expert Basic Scientist Sessions
- Meet The Expert Basic Scientist Sessions
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  - Breaking down signalling in hypogonadotropic hypogonadism
    
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  - Senescence in peadiatric pituitary tumours
    
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  - Beta is better: current progress in preserving and restoring beta cell function
    
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Meet The Expert Sessions
- Meet The Expert Sessions
- - Fertility matters: exploring the impact of lipodystrophy
    
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  - Management of ACC during the ages
    
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  - Hot-Topic Osteoanabolic therapies: when to choose what
    
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  - Management of endocrinopathies induced by cancer therapy
    
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  - Management of the child with ambiguous genitalia
    
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  - Diagnosing and managing AVP excess
    
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  - Hormone treatment in transgender teenagers
    
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  - Management of Adrenal incidentaloma
    
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  - Type 1 diabetes in athletes
    
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Pre-Congress Courses
- Pre-Congress Courses
- - Introduction: Case Mentimeter
    
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  - Sonographic assessment of the thyroid gland, diffuse thyroid illness including autoimmune disease
    
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  - Welcome
    
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  - Session 2: PCOS and the HPG axis: Alterations of the hypothalamo pituitary-gonadal axis in animal models of PCOS
    
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  - Session 3: PCOS and the Brain: PCOS and the Brain
    
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  - Session 4: periphery-brain communication in pcos and metabolic co morbidities: autonomic brain-liver communication in metabolic diseases
    
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Nurses' Pre-Congress Course
- Nurses' Pre-Congress Course
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  - Diabetes from cardle to grave - Growing up with diabetes
    
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Nurses' Sessions
- Section
- - A nurse-led transition clinic: Good example and nurse roles in transitional care
    
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  - Fertility in Patients with CAH
    
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Guidelines
- Guidelines
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How Do I Sessions
- How Do I Sessions
- - How do I evaluate and manage arginine vasopressin deficiency and arginine vasopressin resistance?
    
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  - How do I diagnose and manage adolescence with PCOS?
    
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  - How do I manage the adolescent with Congenital Adrenal Hyperplasia
    
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Oral Communications
- Oral Communications 1: Adrenal and Cardiovascular Endocrinology
- - Biochemical profile, age at diagnosis and patient ancestry are associated with the risk for positive genetic testing for PPGL susceptibility genes
    
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  - Evaluation of microRNAs as liquid biopsy markers n adrenocortical tumours
    
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  - Quantitative proteomics of pediatric adrenocortical tumors reveals a continuum of molecular alterations and identifies prognostically relevant subgroups
    
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  - Pediatric adrenocortical tumors (pACTs) reveal typical patterns of impaired relative activities of steroid metabolizing enzymes
    
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  - Clinical predictors of treatment response in advanced adrenocortical carcinoma: a multicentre ENSAT study
    
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  - Single-cell, single-nucleus, and spatial transcriptomics reveal the cellular atlas and developmental mechanisms of aldosterone-producing micronodules and adenomas
    
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- Oral Communications 2: Diabetes and Insulin Part 1
- - War-provoked glycemic shift: 4-years dynamics of HbA1c levels in Ukrainian population
    
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  - Early detection of type 1 diabetes through population-based antibody screening: design and initial results from the adir program in Israel
    
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  - Novel insights in understanding the relation of glycemic excursions and concomitant sleep macro- and micro-architecture among adolescents with type 1 diabetes
    
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  - Rebound hyperglycemia in children with type 1 diabetes using automated insulin delivery
    
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  - In-hospital diabetes management by a diabetes team using insulin algorithms with continuous glucose monitoring or point-of-care testing in patients with type 2 Diabetes: the DIATEC RCT
    
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  - Delayed puberty and early-onset type 2 diabetes: a nationwide cohort study of 1.6 million adolescents
    
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- Oral Communications 3: Metabolism and Aging
- - Fecal microbiota transplantation improves diabetic kidney disease by regulating gut tryptophan metabolism
    
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  - Epigenetic aging in turner and klinefelter syndrome: correlations with clinical aging markers
    
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  - Role of clock gene Bmal1 in mitochondrial function and lipid metabolism in skeletal muscle
    
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  - Nuclear resident AMPK ?2 enhances adipose tissue browning through Neuregulin 4
    
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  - Modeling adipose tissue dysfunction in polycystic ovary syndrome in vitro using 2D and 3D cell culture systems
    
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  - Sedentary behavior, physical activity, and risk of mortality in adults with obesity
    
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- Oral Communications 4: Pituitary, Neuroendocrinology and Puberty Part 1
- - Differential temporal onset of kisspeptin action following intranasal and intravenous administration supports a novel human olfactory-reproductive pathway
    
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  - B2R overexpression in resistant prolactinomas promotes B2R-D2R dimerization, with B2R precluding D2R signalling generating resistance to D2R agonists
    
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  - Exploration of pituitary stem cells heterogeneity and their contribution in gonadotroph tumors
    
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  - SDHB loss in anterior pituitary embryonic progenitors and postnatal SOX2+ stem cells is insufficient to drive pituitary tumorigenesis and results in pituitary hypoplasia in mice
    
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  - Glucocorticoid negative feedback in regulating hypothalamic-pituitary-adrenal axis: the epigenetic role of miR-27
    
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  - Multi-omics analysis of USP8 mutated and wild type corticotroph pituitary tumors enhances understanding of tumorigenesis, proliferation, immune response and hormone excess in Cushing's disease
    
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- Oral Communications 5: Reproductive and Developmental Endocrinology Part 1
- - Autoimmune diseases in 30,340 Danish women with polycystic ovary syndrome (PCOS) before and after PCOS diagnosis and in 151,520 controls. A national cohort study
    
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  - PCOS-like hyperactivity in the reproductive axis following arcuate nucleus-specific progesterone receptor knockdown
    
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  - Building 3D ovaroids to understand mechanisms of human ovary formation and its pathologies
    
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  - The effect of intranasal insulin on post prandial thermogenesis in obese women with and without polycystic ovary syndrome
    
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  - Gonadotropin rise following intranasal kisspeptin administration is heightened in women with hypothalamic amenorrhoea compared to healthy women
    
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- Oral Communications 7: Bone and Mineral Metabolism
- - Bone mineral density and biochemical parameters after one year of treatment with denosumab or zoledronate in postmenopausal women with osteoporosis and primary hyperparathyroidism: a pilot study
    
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  - Diagnostic performance of parathyroid 4d-ct in men1 syndrome-associated primary hyperparathyroidism
    
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  - The prevalence of neurodevelopmental disorders in a large UK cohort of children with achondroplasia
    
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  - Long-term height gain and maintenance of treatment effect in children with achondroplasia receiving vosoritide
    
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  - Effects of navepegritide on bone morphometry in children with achondroplasia: 52-week results from the approach clinical trial
    
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  - Hippocampal malrotation and transverse temporal sulcus abnoramlities: sensitive and specific neuroradiological markers of hypochondroplasia
    
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  - Sustained normalization of mineral homeostasis in autosomal dominant hypocalcemia type 1: results from a phase 2 study over 42 months of encaleret (cltx-305) treatment
    
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  - Differential regulation of phosphate transport in epididymis and prostate: implications for sperm motility in mice and men
    
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  - Long-term efficacy and safety of palopegteriparatide treatment in adults with chronic hypoparathyroidism: 4-year results from the phase 2 path forward trial
    
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- Oral Communications 8: Diabetes and Insulin Part 2
- - Economic disparities and gender differences in pediatric diabetes Care: the SWEET international Registry
    
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  - Lipid profile in children living with Type 1 Diabetes: A novel approach using Z-scores for standardized comparison
    
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  - The Proof of Concept INCEPTR trial 12 month outcomes - Intracutaneous islet transplant in humans into pre-vascularised Novosorb® neodermis
    
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  - Crosstalk between neuronal mitochondrial dynamics and microglial activation during the hypoglycemic neuronal damage progression with cognitive deficit
    
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  - Redefining islet adaptations in human pregnancy: insights from immunohistochemistry and proteomics
    
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  - Ga-Exendin-4-guided surgery in children with congenital hyperinsulinism (CHI)
    
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- Oral Communications 9: Endocrine Related Cancer
- - Cellular tumor microenvironment cross-talk in pediatric adrenocortical tumors: insights from single-nucleus RNA sequencing
    
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  - Characterization of metastatic dissemination in Znrf3/Trp53 double knock-out mouse model
    
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  - Genetic and functional heterogeneity in aldosterone producing adenomas
    
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  - Clinical and mechanistic implication of aspartyl-tRNA synthetase (DARS1) in the transition from MASLD to hepatocellular carcinoma
    
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  - Acromegaly and cancer - a nationwide study in Sweden 1991-2018
    
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- Oral Communications 10: Pituitary, Neuroendocrinology and Puberty Part 2
- - Single-nucleus multiome profiling of the arcuate-median eminence complex in male marmosets provides molecular insights into the postnatal dynamics of the hypothalamic-pituitary-gonadal axis
    
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  - PSA as a marker of androgen activity during pubertal transition in healthy boys
    
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  - Nuclear factor I/B interaction with PROP1 and its role in pituitary cell differentiation
    
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  - Unravelling the core regulatory network controlling stem cell fate in the anterior pituitary
    
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  - Characterization of hormone-secreting hiPSC-derived pituitary organoids
    
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  - Hydroxytyrosol mitigates high-fat diet-induced precocious puberty in rats through gut microbiome remodeling
    
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- Oral Communications 11: Thyroid Part 1
- - Retrospective, multicentre evaluation of the clinical features and associated diagnostic challenges of central congenital hypothyroidism in the UK
    
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  - Functional non-coding variants in a TTTG microsatellite on chromosome 15q26.1 are a common genetic etiology of congenital hypothyroidism, and present with a mild phenotype
    
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  - Subclinical hyperthyroidism, cardiovascular disease and all-cause mortality: insights from a large DUTCH primary care cohort study
    
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  - Use of thyroid hormones in euthyroid patients: results of an international survey among thyroid experts
    
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  - Efficacy and safety of veligrotug (VRDN-001), a full antagonist monoclonal antibody to IGF-1 receptor, in active thyroid eye disease (TED): THRIVE phase 3 topline results
    
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  - Evaluation of pediatric thyroid nodules with K-TIRADS, ACR-TIRADS, and clinical risk factors
    
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- Oral Communications 13: Adrenal and Cardiovascular Endocrinology Part 2
- - Hydrocortisone treatment only partially restores systemic dysregulations caused by cortisol deficiency in a 21-hydroxylase deficient zebrafish model
    
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  - Towards durable genomic editing for the treatment of congenital adrenal hyperplasia
    
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  - Home measurement of 24-hour corticosteroid dynamics in primary aldosteronism
    
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  - Cardiovascular risk factors in transgender adolescents before and during puberty suppression and sex steroid therapy
    
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  - The incidence of adrenal crisis in addison's disease is low a survey of the national norwegian registry
    
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  - A double-blind study of modified-release hydrocortisones, chronocort versus plenadren, in adrenal insufficiency (CHAMPAIN)
    
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- Oral Communications 14: Growth Axis and Syndromes
- - SEENEZ trial: Near adult height after withdrawing growth hormone treatment in mid-puberty in adolescents with transient idiopathic isolated growth hormone deficiency
    
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  - Chemogenic activation of growth hormone-releasing hormone neurons stimulates the luteinizing hormone secretion
    
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  - Insulin promotes the expression of aromatase in growth plate chondrocytes by activating the PI3K/AKT signaling pathway and enhancing the activity of the CYP19A1 specific promoter
    
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  - Results of the foresiGHt trial support the efficacy and safety of once-weekly lonapegsomatropin in adults with growth hormone deficiency (GHD)
    
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  - Noonan syndrome in real life: Patient characteristics and response to growth hormone therapy in a genetically defined single-country multicentre cohort
    
    ea0110oc14.5
  - Effects of navepegritide on growth in children with achondroplasia: 52-week results from the approach clinical trial
    
    ea0110oc14.6
- Oral Communications 15: Metabolism, Nutrition and Obesity
- - Real-world setmelanotide changes in BMI in French patients with acquired hypothalamic obesity
    
    ea0110oc15.1
  - Long-term results for diazoxide choline extended-release (DCCR) tablets in patients with prader-willi syndrome: developmental behaviour checklist 2 response and relationship to hyperphagia reductions
    
    ea0110oc15.2
  - Long-term outcomes of sleeve gastrectomy in paediatric and transition age patients with prader-willi syndrome: a 5-year longitudinal study
    
    ea0110oc15.3
  - FetuinA connects hepatic steatosis and islet lipid accumulation in HFD mice: inhibiting TLR4 to protect beta cell function therein
    
    ea0110oc15.4
  - SMG7 as a potential contributor to the progression of chronic liver disease to hepatocellular carcinoma
    
    ea0110oc15.5
  - Sex-specific molecular effects of semaglutide on cardiac and hepatic mitochondrial respiration and cellular redox state in HFpEF and MASLD
    
    ea0110oc15.6
- Oral Communications 16: Reproductive and Developmental Endocrinology Part 2
- - Human sex-determination and associated pathologies as a model to understand developmental gene regulation
    
    ea0110oc16.1
  - Characterising the metabolism of 11Oxy-androgens in placental cell models, tissue homogenates and explants
    
    ea0110oc16.2
  - Exposure to phthalates at the masculinization programming window is associated with longer anogenital distance and reduced birth weight in healthy children: A COPANA cohort study of 589 infants
    
    ea0110oc16.3
  - Testosterone therapy and the risk of atrial fibrillation, venous thromboembolism and cardiovascular events in cisgender men with hypogonadism and transgender men
    
    ea0110oc16.4
  - Histological markers of testicular health and spermatogenesis in transgender adolescent girls following puberty suppression and subsequent gender-affirming hormone therapy
    
    ea0110oc16.5
  - Testicular function in young men and risk of cardiometabolic disease up to 20 years later - a register-based follow-up study of more than 5000
    
    ea0110oc16.6
Rapid Communications
- Rapid Communications 1: Adrenal and Cardiovascular Endocrinology
- - Role of postural test in differentiating from primary aldosteronism to low-renin hypertension
    
    ea0110rc1.1
  - Clinical and biochemical determinants of left ventricular hypertrophy and its severity in primary aldosteronism: insights from the SPAIN-ALDO registry
    
    ea0110rc1.2
  - Long-term cardiovascular outcomes after adrenalectomy in mild autonomous cortisol secretion: results from the multicentric ENSAT NAPACA outcome study
    
    ea0110rc1.4
  - Integrated liquid biopsy approach as disease monitoring tool in adrenocortical carcinoma: a preliminary study
    
    ea0110rc1.5
  - Metabolic phenotype in non-aldosterone producing adrenal adenomas (NAPACAs) with co-existent polycystic ovaries syndrome (PCOS): a joint ENSAT project
    
    ea0110rc1.6
- Rapid Communications 2: Diabetes and Insulin Part 1
- - Stable age at diagnosis and persistently high incidence of inaugural diabetic ketoacidosis in children with type 1 diabetes: insights from french diabetic ketoacidosis observatory (2010-2023)
    
    ea0110rc2.1
  - Migration background 2000-2023 in type 1 and 2 diabetes, analysis based on the DPV registry: children with Turkish background at increased risk to develop type 2 diabetes - independent of their BMI
    
    ea0110rc2.2
  - Islet cell autoimmunity and preclinical phase of type 1 diabetes in general population of 1-9 year old children in north-eastern region of Poland - a summary of the first 18 months of the study
    
    ea0110rc2.3
  - Transition of youth with type 1 diabetes from pediatric to adult care in Europe: Insights from centers participating in the international sweet initiative
    
    ea0110rc2.4
  - Developing a multicentre surveillance system for hyperosmolar hyperglycaemic syndrome: a framework for implementation and findings
    
    ea0110rc2.5
  - Isolated glucosuria in adolescence and early-onset type 2 diabetes: a nationwide cohort study of 1.6 million adolescents
    
    ea0110rc2.6
- Rapid Communications 3: Metabolism and Aging
- - Genotype-histotype-phenotype correlations in atypical congenital hyperinsulinism
    
    ea0110rc3.1
  - An ongoing phase 2 study of efpegerglucagon: promising results on safety and efficacy in subjects with congenital hyperinsulinism
    
    ea0110rc3.2
  - Modulation of SIRT1-related microRNAs in differentiating adipocytes and their relationship with inflammation
    
    ea0110rc3.3
  - Sensitivity to thyroid hormones and glomerular hyperfiltration in children and adolescents with overweight or obesity
    
    ea0110rc3.4
  - Delivery mode is associated with persistent changes of steroid hormone levels in boys at three months of age - a COPANA study of 508 healthy infants
    
    ea0110rc3.5
  - Efficacy and safety results from a pivotal phase 3 trial of DTX401, an AAV8-mediated liver-directed gene therapy, in individuals with glycogen storage disease type Ia (GSDIa)
    
    ea0110rc3.6
- Rapid Communications 4: Pituitary, Neuroendocrinology and Puberty Part 1
- - Targeted correction of plasma sodium in hospitalized patients with chronic hyponatremia
    
    ea0110rc4.1
  - Melatonin as a possible stimulus to unmask an oxytocin deficient state in hypopituitarism and hypothalamic damage
    
    ea0110rc4.2
  - Clofutriben inhibits 11sz-hydroxysteroid dehydrogenase type 1 and improves ACTH-dependent cushing's syndrome compared with placebo in a phase II trial (RESCUE)
    
    ea0110rc4.3
  - Results from the core phase of the open-label, phase 3 ACROINNOVA 2 trial: CAM2029, a subcutaneous octreotide depot, achieves sustained, long-term biochemical control in acromegaly
    
    ea0110rc4.4
  - Efficacy and safety of once-weekly somatrogon in adults with growth hormone deficiency: a phase 3 study
    
    ea0110rc4.5
  - Comparison of long-acting and short-acting GLP-1 receptor agonists on copeptin in euvolemic participants - a secondary analysis of three prospective trials
    
    ea0110rc4.6
- Rapid Communications 5: Reproductive and Developmental Endocrinology Part 1
- - Excess adrenal androgen secretion is a consequence of in utero androgen excess in an ovine model of PCOS
    
    ea0110rc5.1
  - Comparison of oxytocin and incretin dynamics in response to food intake in women with polycystic ovary syndrome and healthy controls
    
    ea0110rc5.2
  - The kisspeptin/nNOS/GnRH (KiNG) neuronal network: regulating reproductive function through a dual activation-inhibition mechanism
    
    ea0110rc5.3
  - Kisspeptin-54 accurately identifies the cause of delayed puberty
    
    ea0110rc5.4
  - The predictive value of AMH and FSH concerning spontaneous vs induced puberty: a retrospective, longitudinal study of 50 girls with Turner Syndrome
    
    ea0110rc5.5
  - Low prolactin levels as a risk factor for gestational diabetes mellitus: a longitudinal cohort study
    
    ea0110rc5.6
- Rapid Communications 8: Diabetes and Insulin Part 2
- - Study of predictive markers determining poor response to finerenone therapy in the management of diabetic kidney disease
    
    ea0110rc8.1
  - Efficacy and safety of finerenone in people with chronic kidney disease and type 2 diabetes by treatment goal attainment: A FIDELITY analysis
    
    ea0110rc8.2
  - Deviations in guideline implementation lead to severe hypoglycemia in diabetic ketoacidosis management
    
    ea0110rc8.3
  - Congenital hyperinsulinism and diabetes later in life -dominant variants causing both phenotypes
    
    ea0110rc8.4
  - Assessment of derangements in glucose metabolism in children with transfusion dependent thalassemia: a cross sectional analytical study
    
    ea0110rc8.5
  - Inherited stress vulnerability exacerbates obesity-induced metabolic alterations through dysfunctional adipose tissue
    
    ea0110rc8.6
- Rapid Communications 9: Endocrine Related Cancer
- - Hereditary duodenopancreatic neuroendocrine tumors, what genetic analysis? a retrospective analysis on 410 patients
    
    ea0110rc9.1
  - Dysregulation of a RNA exosome component: a driving force behind prostate cancer progression
    
    ea0110rc9.2
  - Defining the clinical value of circulating splicing factors in prostate cancer: SRRM1 as a novel predictive biomarker and exploitable therapeutic target
    
    ea0110rc9.3
  - Adipsic arginine vasopressin deficiency in CNS tumour patients: clinical management challenges
    
    ea0110rc9.4
  - Preclinical development and first clinical use of a radioiodinated CYP17 inhibitor for adrenal theranostics
    
    ea0110rc9.5
- Rapid Communications 10: Pituitary, Neuroendocrinology and Puberty Part 2
- - Recessive truncations in a previously uncharacterized gene, CCDC149, are a novel cause of congenital hypopituitarism
    
    ea0110rc10.1
  - Transcriptomic classification of PIT1-lineage PitNETs reveals distinct molecular groups associated with tumor differentiation and treatment resistance
    
    ea0110rc10.2
  - TNIP1 as a key regulator in sparsely granulated somatotropinomas: a combined proteomics and bioinformatics approach
    
    ea0110rc10.3
  - Sustained DNA methylation changes despite biochemical remission in cushing's disease
    
    ea0110rc10.4
  - Histotype is not associated with short- or long-term remission of somatotroph tumours
    
    ea0110rc10.5
  - Hypothalamic obesity following craniopharyngioma surgery; what is the role of hypothalamic inflammation?
    
    ea0110rc10.6
- Rapid Communications 11: Thyroid Part 1
- - Medullary thyroid carcinoma and pathogenic ret proto-oncogene variants in children: clinical outcomes following prophylactic/therapeutic thyroidectomy
    
    ea0110rc11.1
  - Different thyroid hormone profiles in women with euploid compared to aneuploid pregnancy loss - a prospective cohort study
    
    ea0110rc11.2
  - Proteomics-based identification of novel biomarkers for assessing severity and predicting recurrence in graves' thyrotoxicosis
    
    ea0110rc11.3
  - The role of ferroptosis as a novel alternative cell death model in thyrocytes from Hashimotos thyroiditis patients
    
    ea0110rc11.4
  - Thyrosense - a sensing device for monitoring of thyroid-stimulating hormone
    
    ea0110rc11.5
  - Evaluation of congenital hypothyroidism cases diagnosed through newborn screening and predictive factors for transient forms
    
    ea0110rc11.6
- Rapid Communications 13: Adrenal and Cardiovascular Endocrinology Part 2
- - Constitutional duplication of PRKACA causes primary pigmented nodular adrenocortical disease (PPNAD) and generates new chromatin interactions
    
    ea0110rc13.1
  - Imaging bias in patients with adrenal adenomas
    
    ea0110rc13.2
  - Adrenal aldosterone synthase (CYP11B2) histopathology and its association with disease-induced sudden death
    
    ea0110rc13.3
  - Primary adrenal insufficiency in the young, consider APS-1
    
    ea0110rc13.4
  - Crinecerfont improves reproductive hormones in classic congenital adrenal hyperplasia: 1-year results from the phase 3 CAHtalyst™ adult study
    
    ea0110rc13.5
  - Crinecerfont enables glucocorticoid dose reductions while maintaining/improving androstenedione in paediatric patients with congenital adrenal hyperplasia: subgroup analyses from CAHtalyst™ paediatric
    
    ea0110rc13.6
- Rapid Communications 14: Growth Axis and Syndromes
- - Long-term efficacy and safety of once-weekly somapacitan in children with growth hormone deficiency: 7-year results from the randomised REAL 3 trial
    
    ea0110rc14.1
  - Unexpected unbalanced upregulation of genes in gene replacement therapy with a constitutively active promoter and growth hormone receptor (GHR) in mice with nonfunctional GHR (laron mice)
    
    ea0110rc14.2
  - AKT and PI3K inhibitors are more efficient in inhibiting growth of Proteus syndrome patient cells compared to mTOR inhibition
    
    ea0110rc14.3
  - Neurodevelopmental outcomes in silver russell syndrome: the impact of molecular causes
    
    ea0110rc14.4
  - Pituitary gigantism: what differences beyond height can we expect compared to acromegaly? a comparison of clinical features and mortality in 3244 patients
    
    ea0110rc14.5
  - Identification of novel genetic variants associated with short stature using whole exome sequencing: insights from a pediatric cohort
    
    ea0110rc14.6
- Rapid Communications 15: Metabolism, Nutrition and Obesity
- - Age of onset of hyperphagia and/or obesity as key predictors of a positive genetic test for POMC, PCSK1 or LEPR deficiency or BBS
    
    ea0110rc15.1
  - Setmelanotide treatment in individuals with obesity and PHIP variants: results from the DAYBREAK trial
    
    ea0110rc15.2
  - Premature aging in alstrom syndrome: a model of monogenic syndromic obesity
    
    ea0110rc15.3
  - Long-term weight gain in children who underwent adenotonsillectomy
    
    ea0110rc15.4
  - A metabolomic signature of maternal BMI is associated with pregnancy complications: insights from the COPSAC2010 and VDAART mother-child cohorts
    
    ea0110rc15.5
  - Brown adipose tissue as nutrient buffer through diet-induced thermogenesis
    
    ea0110rc15.6
- Rapid Communications 16: Reproductive and Developmental Endocrinology Part 2
- - Genotype-phenotype correlation in patients having a WT1 germline variant : lessons from a large French cohort
    
    ea0110rc16.1
  - Steroidogenesis and CYP17A1 inhibition: development of potent inhibitors for adrenal and gonadal steroid biosynthesis
    
    ea0110rc16.2
  - Testicular contributions to masculinization in HSD17B3 deficiency: the critical role of HSD17B12
    
    ea0110rc16.3
  - Semen quality and lifespan - a study of 78,284 men followed for up to 50 years
    
    ea0110rc16.4
  - Smart menstrual health monitoring patch: a non-invasive ai-driven solution for cycle tracing
    
    ea0110rc16.5
  - Examining factors associated with androgen abuse withdrawal symptoms during the first year of cessation: a cross-sectional study of 286 men
    
    ea0110rc16.6
Poster Presentations
- Adrenal and Cardiovascular Endocrinology
- - Stimulated peak cortisol in healthy paticipants measured during the insulin tolerance test: defining cut-off limits for adrenal insufficiency with two generations of Roche cortisol immunoassays
    
    ea0110p1
  - Neonatal screening in subjects with non-classic congenital adrenal hyperplasia (NCCAH)
    
    ea0110p2
  - Relacorilant improved blood pressure and maintained other cardiometabolic improvements in long-term study in patients with endogenous hypercortisolism (Cushing syndrome)
    
    ea0110p3
  - Initial findings of the study into the health status of adults with CAH in the UK and Ireland - CaHASE2
    
    ea0110p31
  - is imaging alone sufficient for lateralising PA in younger patients?
    
    ea0110p32
  - Challenges in the interpretation of cortisol response during insulin tolerance test: prevalence of secondary adrenal insufficiency and predictive factors
    
    ea0110p33
  - The relationship between androgens and autistic traits: a comparative study in children with congenital adrenal hyperplasia
    
    ea0110p34
  - Adrenal dysfunction and cardiometabolic comorbidities associated with weight cycling in postmenopausal conditions
    
    ea0110p35
  - Chronotherapy with once-daily osilodrostat is safe and effective in Cushing's syndrome and restores circadian profile improving quality of life and sleep
    
    ea0110p36
  - Assessment of adrenal function after oral prednisolone therapy in children with epileptic spasms
    
    ea0110p37
  - Brain and behavior in primary adrenal insufficiency - with emphasis on the precuneus & orbitofrontal cortex
    
    ea0110p38
  - Exploring oligogenicity as a contributor to the broad phenotypic spectrum of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study
    
    ea0110p39
  - Understanding the sources of aldosterone and cortisol production in primary aldosteronism and autonomous cortisol secretion
    
    ea0110p40
  - Ready, steady, go: an exploration of the knowledge and self-management skills of patients with congenital adrenal hyperplasia during transition
    
    ea0110p41
  - Neurocrine regulation of aldosterone secretion: The role of substance P and NK1 receptor in aldosterone-producing adenomas
    
    ea0110p42
  - Molecular mechanisms of glucocorticoid sensitivity: insights from a novel transgenic mouse model
    
    ea0110p43
  - Real word incidence of adrenal insufficiency after long-terme use os systemic and inhaled corticosteroids
    
    ea0110p44
  - Real-world experience with 68Ga-Pentixa for positron emission tomography in the management of primary aldosteronism
    
    ea0110p45
  - A retrospective longitudinal study on the association between urine metanephrines and cardiovascular events in patients in primary prevention without chromaffin tumors
    
    ea0110p46
  - Circadian dysregulation of metabolic pathways in different states of cortisol excess and insufficiency
    
    ea0110p47
  - Cardiac function and morphology in patients with adrenal incidentalomas: a longitudinal study
    
    ea0110p48
  - Correlation of morning cortisol with HPA axis response to insulin-induced hypoglycemia in children
    
    ea0110p49
  - Pseudohypoaldosteronism in infantile atopic dermatitis: a case series
    
    ea0110p50
  - Real-life evaluation of efficacy and safety of modified-release hydrocortisone (MR-HC) in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A national cohort study
    
    ea0110p51
  - WHAT\..IF? Organizing a focus group for young adults with congenital adrenal hyperplasia who underwent feminizing surgery in childhood and/or adolescence
    
    ea0110p52
  - Aldosterone synthase (CYP11B2) immunostaining predicts outcome in unilateral primary aldosteronism
    
    ea0110p53
  - High prevalence of CYP11B2-positive aldosterone-producing micronodules in subjects without known adrenal diseases
    
    ea0110p54
  - Advancing adrenal tissue analysis: A comprehensive guide to immunohistochemical evaluation, RNA-scope, and digital pathology with QuPath
    
    ea0110p55
  - Long-term outcomes and prognostic value of LC-MS/MS hormone profiling in the largest single-center cohort of adrenocortical carcinoma: a cohort study since 2000
    
    ea0110p56
  - Adrenalectomy reduces the risk of vertebral fractures in patients with adrenal adenoma and mild autonomous cortisol secretion
    
    ea0110p57
  - Pediatric adrenal incidentalomas: Insights from a multicenter study on diagnosis and outcomes
    
    ea0110p58
  - Adrenomedullary stem cells can instigate the formation of steroidogenic adrenal cortex through paracrine signalling
    
    ea0110p59
  - Adrenal insufficiency associated with mutations in haem biosynthesis genes
    
    ea0110p60
  - Lipoid congenital adrenal hyperplasia due to mutations in StAR: Genotype and phenotype in 10 Vietnamese patients
    
    ea0110p61
  - Growth-promoting therapy in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Real-world data from the I-CAH registry
    
    ea0110p62
  - Influence of glucocorticoid replacement and dosage on infection rates and adrenal crises in patients with adrenal insufficiency
    
    ea0110p63
  - Systemic treatment and outcomes in metastatic pheochromocytomas and paragangliomas of a multicenter Spanish cohort
    
    ea0110p64
  - Factors influencing the time to achieve target mitotane concentration
    
    ea0110p65
  - Diurnal aldosterone and potassium intake in third trimester are associated with higher blood pressure in offspring up to 5 years of age
    
    ea0110p66
  - Activation of calcium signaling, using chemogenetic tools, leads to the development of hyperaldosteronism and adrenal remodeling in mice
    
    ea0110p67
  - Investigating the role of insulin and adipose tissue in regulating adrenal steroidogenesis in response to metabolic diseases
    
    ea0110p68
  - Medical treatment of hypercortisolism with relacorilant: Final results of the phase 3 GRACE study
    
    ea0110p69
  - PLK1 and multi-CDKs dual inhibition as a novel approach for the treatment of adrenocortical carcinomas
    
    ea0110p70
  - Is muscle strength an overlooked parameter in patients affected by mild autonomous cortisol secretion (MACS)? A prospective study
    
    ea0110p71
  - Exploring the impact of pathogenic variants and cortisol secretion on M2-like tumor-associated macrophage polarization in adrenocortical adenomas
    
    ea0110p72
  - Diagnostic accuracy of urinary free cortisol and cortisone excretion for the diagnosis of neoplastic hypercortisolism
    
    ea0110p73
  - Increased mortality in patients with primary adrenal insufficiency: a systematic review and meta-analysis
    
    ea0110p74
  - Prediction of lateralisation in primary aldosteronism - a decision tree model for bypassing adrenal vein sampling in bilateral disease
    
    ea0110p75
  - The genetic and functional analysis of CYP21A2 mutants in congenital adrenal hyperplasia
    
    ea0110p76
  - The impact of alternative treatment approaches on final adult height in patients with congenital adrenal hyperplasia
    
    ea0110p77
  - Diagnostic work-up of paediatric adrenocortical tumours - International consensus through a modified Delphi process
    
    ea0110p78
  - Once-daily low-dose prednisolone has lower cardiovascular risk than conventional hydrocortisone replacement therapy in adrenal insufficiency: A double-blind randomised controlled trial
    
    ea0110p79
  - Evaluation of the overnight dexamethasone suppression test in a large cohort of patients with incidentally discovered adrenal nodules
    
    ea0110p80
  - Thyroid hormone regulation of adrenal androgens: Observations from the H295R cell model and pediatric CAH patients
    
    ea0110p81
  - -hour blood pressure profiles in patients with adrenal insufficiency
    
    ea0110p82
  - GC-MS urinary steroid metabotyping of aldosterone deficient states
    
    ea0110p83
  - Metabolic associations of premature adrenarche 4 years after menarche
    
    ea0110p84
  - Myocardial microcirculation and left ventricular function in former and current female androgenic anabolic steroid users: A cross-sectional study
    
    ea0110p85
  - Predictors of increased vulnerability for adrenal crises in patients with chronic adrenal insufficiency - long-term follow-up of an initial prospective study
    
    ea0110p86
  - Treatment of children and adolescents with congenital adrenal hyperplasia with hydrocortisone modified-release hard capsules
    
    ea0110p87
  - AZD1775: effect of monotherapy or EDP-M combination in the treatment of ACC preclinical models
    
    ea0110p88
  - Adrenalectomy ameliorates cardiovascular profile in patients with mild autonomous cortisol secretion: results of a RCT
    
    ea0110p89
  - Assessing hypothalamus-pituitary-adrenal axis in Prader-Willi syndrome: experience in a tertiary care centre
    
    ea0110p90
  - Intraocular pressure and risk of glucocorticoid-induced ocular hypertension are increased in children with congenital adrenal hyperplasia
    
    ea0110p91
  - Analysis of novel ventricular repolarization parameters in Cushing's syndrome: A comparative study
    
    ea0110p92
  - Assessment of adrenal function after glucocorticoid therapy for childhood onset first episode nephrotic syndrome
    
    ea0110p93
  - Insights into the health provision for children with congenital adrenal hyperplasia in the UK and implementation of longitudinal collection and analysis of real-world data
    
    ea0110p94
  - Increased prevalence and incidence of psychiatric and sleep disorders in patients with non-functional adrenal tumors
    
    ea0110p95
  - Macrophage polarisation in patients with autonomous cortisol excess
    
    ea0110p96
  - Aldosterone, renin and their ratio (ARR) in patients with newly diagnosed and untreated hypertension
    
    ea0110p99
  - Incidental adrenal nodules: A single-center study on the prevalence and radiological predictors of phaeochromocytoma
    
    ea0110p100
  - Effects of prednisolone administration on clock gene expression and indices of circadian rhythms in healthy human subjects
    
    ea0110p101
  - Metabolomic profiling of premature adrenarche reveals a unique acylcarnitine-dominated signature
    
    ea0110p102
  - The determination of steroid levels directly in the tissue of bilateral adrenocortical lesions reveals discrepancies with circulating levels
    
    ea0110p103
  - Circulating GDF-15 is elevated in adrenal cushing's syndrome but not in cushing's disease
    
    ea0110p104
  - Unravelling the sexually dimorphic role of adrenocapsular progenitor cells during stress adaptation of the adult adrenal gland
    
    ea0110p105
  - Diagnostic genotyping of CYP21A2 gene employing Short Read-NGS: Benefits and Limitations
    
    ea0110p106
  - Elevated bone turnover in primary aldosteronism: a role for aldosterone-dependent phosphate changes?
    
    ea0110p107
  - Serum inflammation-based scores in adrenal incidentalomas: the role of salivary cortisol rhythm dysregulation
    
    ea0110p108
  - Spectrum of Presentation of 46,XY Sex Reversal and Adrenal Insufficiency: Case Report with Literature Review
    
    ea0110p109
  - Diagnostic accuracy of urinary aldosterone, independent of sodium intake, for the diagnosis of primary aldosteronism
    
    ea0110p110
  - Adrenocortical carcinoma following long-term stable adrenocortical adenomas: a rare phenomenon in a large cohort
    
    ea0110p111
  - Metabolic syndrome in patients treated for primary adrenal insufficiency
    
    ea0110p112
  - Oral Contraceptives: A Key to reducing androgen levels in women with classic CAH
    
    ea0110p113
  - Exploring the role of glucocorticoids and androgens in the regulation of brain immunity using zebrafish models of impaired steroidogenesis
    
    ea0110p114
  - Effect of very low LDL cholesterol levels on steroid metabolome
    
    ea0110p115
  - Performance of plasma renin assays in guiding mineralocorticoid dosing in children with adrenal insufficiency
    
    ea0110p117
  - Familial hypercholesterolemia in Chinese children and adolescents: a multicenter study
    
    ea0110p118
  - Effect of cholecalciferol and calcium supplementation on blood pressure in young Infertile but otherwise healthy men
    
    ea0110p119
  - Persistent renin suppression after unilateral adrenalectomy in patients with primary aldosteronism
    
    ea0110p120
  - Establishing the prevalence of non-classical congenital adrenal hyperplasia using serum 21-deoxycortisol concentrations
    
    ea0110p121
  - Can the plasma aldosterone/potassium ratio predict primary aldosteronism in patients scheduled for confirmatory testing?
    
    ea0110p122
  - Significance of plasma catestatin and relaxin-2 levels in patients with primary hypertension and type 2 diabetes mellitus
    
    ea0110p123
  - Education of sick day management of paediatric adrenal insufficiency: a national survey of paediatric endocrine nurse specialists
    
    ea0110p124
  - A validated liquid chromatography mass spectrometry method for comprehensive urinary steroid profiling: applications in hypertension research and diagnostic studies
    
    ea0110p125
  - Space Oil Vapours: Endocrine Risks and the Adolescent Challenges
    
    ea0110p126
  - Implementing a neonatal screening programme for Congenital Adrenal Hyperplasia using liquid chromatography-tandem mass spectometry in a Northern Spanish region
    
    ea0110p127
  - Morning serum cortisol predicts short synacthen test response during glucocorticoid weaning in children and adults
    
    ea0110p128
  - Metabolic disorders in pheochromocytoma: A retrospective multicenter study of pre- and post-operative profiles
    
    ea0110p129
  - Prognostic factors for cardiovascular complications induced by catecholamines in pheochromocytomas and paragangliomas: A systematic review and meta-analysis
    
    ea0110p130
  - Surgical outcomes and histochemical analysis in primary aldosteronism: a 10-year cohort study
    
    ea0110p131
  - Determination of cortisol cut-off limits in the overnight dexamethason suppression test using roche elecsys® cortisol II immunoassay
    
    ea0110p132
  - Urine steroid metabolomics, selected proteins and neuropeptides - new non-invasive diagnostic tools in hormonally active adrenal tumors
    
    ea0110p133
  - Does the cutoff point of 1.8 μg/dl in the 1 mg dexamethasone suppression test differentiate the cardiometabolic risk attributed to MACS?
    
    ea0110p134
  - Efficacy and safety of corticosteroid replacement therapies in pediatric congenital adrenal hyperplasia: insights from hydrocortisone, prednisone, and dexamethasone studies
    
    ea0110p135
  - Evaluating 24-hour urine aldosterone levels with suppressed renin activity as a practical diagnostic tool for primary aldosteronism: a comparison with conventional confirmatory tests
    
    ea0110p136
  - Serum orexin ghrelin and adropin levels in patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency
    
    ea0110p137
  - Evaluation of the frequency of Hashimoto's thyroiditis and thyroid cyto/histopathological findings in patients with Connshing Syndrome
    
    ea0110p138
  - The prevalence and the diagnosis of glucocorticoids-induced adrenal insufficiency: a systematic review
    
    ea0110p139
  - Lowering the day 5 postoperative cortisol cutoff value to avoid over-diagnosis of secondary adrenal insufficiency following pituitary surgery
    
    ea0110p140
  - The genetics of adrenal insufficiency, evolution of methodologies over 35 years in a single centre
    
    ea0110p141
  - Single daily dose prednisolone has a lower cardiovascular risk compared to multiple daily hydrocortisone doses in patients with adrenal insufficiency
    
    ea0110p142
  - Clinical characteristics and outcomes in 31 pediatric cases of x-linked adrenoleukodystrophy: a retrospective study at SCMC
    
    ea0110p143
  - ESPE school: sharing knowledge to save lives - developing and standardizing education for clinicians and families with children with adrenal insufficiency in Kazakhstan
    
    ea0110p144
  - Smoking and alcohol use plays a mediating role on the social determinants of high blood pressure: evidence from nationally representative sample in India
    
    ea0110p145
  - Management practices in Italy on adrenal insufficiency in young people with Duchenne muscular dystrophy on steroid treatment
    
    ea0110p146
  - Increased arterial stiffness and short QTc interval are associated to androgen levels in classical congenital adrenal hyperplasia due to 21 hydroxylase deficiency
    
    ea0110p147
  - Investigation of alternative hormones for evaluating selectivity of adrenal vein sampling in the subtype diagnosis of primary aldosteronism
    
    ea0110p148
  - Dose the GH IGF-1 Axis serve as a determinant of prognosis in Acute Ischemic Stroke?
    
    ea0110p149
  - Impact of gender-affirming hormone therapy on cardiovascular risk factors in transgender individuals
    
    ea0110p150
  - Cortisol response to coffee, tea, and caffeinated drinks: A comparative review of studies
    
    ea0110p151
  - Short-term effect on tissue sodium distribution in hypertensive patients following sodium loading test: A sodium MRI study
    
    ea0110p152
  - Impact of Val334Ile and Val472Leu variants on cytochrome P450 oxidoreductase activity
    
    ea0110p153
  - Education of sick day management in young people with adrenal insufficiency: Online survey and focus groups involving young people and parents
    
    ea0110p154
  - Post adrenalectomy hyperkalemia in primary aldosteronism. A case series of a not well-defined complication
    
    ea0110p155
  - Metabolic risk following gender affirming hormone therapy, a prospective cohort study
    
    ea0110p156
  - Patient-reported outcomes in patients with primary adrenal insufficiency - A study from the register for organ-specific sautoimmune diseases (ROAS)
    
    ea0110p157
  - Clinical characteristics and genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: A case series
    
    ea0110p158
  - Establishment of an adult mouse adrenal ex vivo tissue culture model
    
    ea0110p159
  - Paediatric peripheral adrenal insufficiency: Rare causes in an observational cohort
    
    ea0110p160
  - Contribution of immunohistochemistry and in situhybridization in BMAD and correlations with patient genotype
    
    ea0110p161
  - Direct detection of urinary free cortisol: Analytical and clinical validation of a new fully automated chemiluminescence assay
    
    ea0110p162
  - Characterization of ferroptosis activation in primary mouse spheroids
    
    ea0110p163
  - Treatment of primary aldosteronism improves cardiac autonomic function
    
    ea0110p164
  - Steroidomics in adrenal tumors
    
    ea0110p165
  - Cortisol secretion and its tissue sensitivity are associated with the comorbidities of obese patients without Cushing Syndrome
    
    ea0110p166
  - Impact of adrenal insufficiency on quality of life: clinical insights from a retrospective study
    
    ea0110p167
  - -Oxygenated androgens in healthy young men and women and the impact of hormonal contraceptives.
    
    ea0110p168
  - Androgens as prognostic factors - the evaluation of septic patients
    
    ea0110p169
  - INSM-1 - a new biomarker in the differential diagnosis of adrenal tumor lesions - a preliminary study
    
    ea0110p170
  - Endocrinological adverse effects of abiraterone acetate in the treatment of prostate cancer: Real-world prevalence
    
    ea0110p171
  - Diurnal pattern of secretion of cortisol, Aldosterone and 18-hydroxycortisol levels in four biological fluids in healthy volunteers
    
    ea0110p172
  - Long-term impact of hypercortisolism on diabetes outcomes: A follow-up study
    
    ea0110p173
  - Triple a syndrome: phenotypic and genotypic diversity and a novel AAAS gene variant
    
    ea0110p174
  - Reliability of morning cortisol in predicting the recovery of hypothalamic-pituitary-adrenal (HPA) axis in patients with glucocorticoid induced adrenal insufficiency
    
    ea0110p175
  - WES as a Tool for Differential Diagnosis of Adrenal Insufficiency in Sudanese Children
    
    ea0110p176
  - Cognitive function worsens with increasing age and glucocorticoid dose in classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    
    ea0110p177
  - Evaluation of the metabolic impact of modified-release hydrocortisone in patients with congenital adrenal hyperplasia: an observational cohort study
    
    ea0110p178
  - Active steroidogenesis increases the vulnerability of human adrenocortical cells to SARS-CoV-2 infection
    
    ea0110p179
  - Assessment of the association between cardiometabolic index (CMI) and metabolic dysfunction-associated steatotic liver disease (MASLD): A systematic review and meta-analysis
    
    ea0110p180
  - Is the 18 ng/ml cortisol cut-off at the 1 mg overnight dexamethasone suppression test effective with routine immunoassays? Comparison with LC-MS/MS
    
    ea0110p181
  - Harmonization of serum cortisol methods for dynamic testing
    
    ea0110p182
  - Prevalence and causes of negative genetic testing results in clinically diagnosed congenital adrenal hyperplasia: A research summary
    
    ea0110p183
  - Friedreich ataxia and impaired steroidogenesis
    
    ea0110p184
  - Less for more? Outcomes of adrenal vein sampling over a 5-year interval from a single operator in a specialist referral centre
    
    ea0110p185
  - The follow up of 3 patients with apparent mineralocorticoid excess after 32 years
    
    ea0110p186
  - Clinical significance of mild autonomous cortisol secretion associated with primary aldosteronism
    
    ea0110p187
  - Salt wasting in infancy: Pseudohypoaldosteronism type 1 secondary to a novel genetic mutation
    
    ea0110p188
  - Glucocorticoid receptor isoform expression in peripheral blood mononuclear cells differs in varying states of glucocorticoid exposure
    
    ea0110p189
  - Impact of cholesterol supplementation for critical illness-induced hypocholesterolemia in a mouse model of prolonged sepsis: Effect on muscle weakness and adrenal failure
    
    ea0110p190
  - Suprarenal adenomas in adult Bulgarian CAH patients
    
    ea0110p191
  - Congenital adrenal hyperplasia causing Gender dysphoria: The dilemma of being a boy or a girl?
    
    ea0110p192
  - A novel mutation in a female patient with congenital adrenal hyperplasia due to 11-hydroxylase deficiency: A case report
    
    ea0110p193
  - Quantification of plasma free cholesterol using LC-MS/MS: A potential screening marker for familial hypercholesterolemia in children
    
    ea0110p194
  - Comparison between Romanian and Flemish cohort of patients with PPGLs
    
    ea0110p195
  - Concordance between adrenal CT and adrenal venous sampling in defining laterality and biochemical outcomes in primary hyperaldosteronism
    
    ea0110p196
  - Clinical, biological and genetic characteristics in congenital adrenal hyperplasia due to 11-beta hydroxylase deficiency in a Tunisian center
    
    ea0110p197
  - Evaluation of cardiovascular risk and hepatic fibrosis scores in patients with pheochromocytoma
    
    ea0110p198
  - Ensuring safety in adrenal insufficiency: A review of emergency hydrocortisone kit prescriptions
    
    ea0110p199
- Bone and Mineral Metabolism
- - Consistent reduction in rate of fracture with setrusumab therapy in patients with osteogenesis imperfecta: month 14 data from phase 2 of the orbit study
    
    ea0110p4
  - Pathophysiology of osteoporosis (PATHOS Study): role of hidden cortisol excess (HidHyCo) and its predictors in bone fragility, preliminary results
    
    ea0110p5
  - Parathyroid surgery in children with sporadic and familial hyperparathyroidism
    
    ea0110p6
  - Bone microarchitectural degradation in hypertensive patients: a population study
    
    ea0110p200
  - The effect of low-dose cyclic 17-sz-estradiol administration on bone turnover in healthy postmenopausal women: a randomized controlled trial
    
    ea0110p201
  - Assessing PTH dynamics following total thyroidectomy: an important tool for predicting hypoparathyroidism
    
    ea0110p202
  - Quality of life assessed by HPES and HPQ28 questionnaires in patients with post-surgical hypoparathyroidism: correlation with biochemical and clinical features
    
    ea0110p203
  - Switch from rhpth1-84 to transcon PTH with individual dose adjustment in adult hypoparathyroidism - results for 40 patients one month after treatment transition
    
    ea0110p204
  - Bone health in cleidocranial dysplasia: a large single-centre UK case series and literature review
    
    ea0110p205
  - Serum phosphate as a marker of disease severity in primary hyperparathyroidism
    
    ea0110p206
  - Classification of bone turnover and calcium metabolism markers based on the molecular subtypes of osteogenesis imperfecta
    
    ea0110p207
  - Autosomal dominant hypocalcemia type 1 or type 2: baseline characteristics of pediatric participants in the CLARIFY disease monitoring study
    
    ea0110p208
  - Caloric restriction exerts duration-dependent effects on marrow adiposity, bone structure, & metabolic health
    
    ea0110p209
  - A novel method for the detection of hypercalciuria in individuals with chronic hypoparathyroidism
    
    ea0110p210
  - Cardiovascular disease in patients with post-surgical hypoparathyroidism
    
    ea0110p211
  - Deeplasia: a novel tool for the assessment of bone age in skeletal dysplasia
    
    ea0110p212
  - Switch from rhPTH1-84 to transcon PTH in patients with hypoparathyroidism normalizes phosphate, magnesium metabolism, and bone turnover
    
    ea0110p213
  - Risk of non-completion of sequential osteoporosis therapy after teriparatide treatment - real-life data from Hungary
    
    ea0110p214
  - Wide clinical spectrum of GCM2-related primary hyperparathyroidism
    
    ea0110p215
  - Risk of atypical femoral fractures among osteoporotic patients on denosumab treatment in real-life setting: a population-based study
    
    ea0110p216
  - Histopathological and clinical differences in primary hyperparathyroidism: a retrospective analysis of parathyroid adenomas with severe and mild hypercalcemia
    
    ea0110p217
  - Quantitative evaluation of hypophosphatemic rickets due to ENPP1 deficiency
    
    ea0110p218
  - Preliminary results from a prospective cohort study on real-world data of chronic hypoparathyroidism treated with trans-con PTH
    
    ea0110p219
  - Relation of body composition with 3D-DXA parameters and trabecular bone score in women with anorexia nervosa
    
    ea0110p220
  - Treatment of hypercalciuria in patients with chronic hypoparathyroidism
    
    ea0110p221
  - Effect of thiazide diuretics on bone turnover in osteoporotic postmenopausal patients with idiopathic hypercalciuria
    
    ea0110p222
  - FGF23 in chronic hypoparathyroidism: clinical implications of phosphate regulation
    
    ea0110p223
  - Clinical and phenotypic features of osteogenesis imperfecta caused by fkbp10 mutations: a study of skeletal deformities and cervical abnormalities
    
    ea0110p224
  - The role of FGF23 in phosphorus and calcium metabolism: lessons from diseases affecting serum phosphate levels
    
    ea0110p225
  - Gain-of-function CASR variants identified as a major genetic contributor of non-surgical hypoparathyroidism: findings from over 300 participants in a sponsored genetic testing program
    
    ea0110p227
  - Skeletal characterization of patients with PLS3-associated early onset osteoporosis in comparison to patients with osteogenesis imperfecta type i
    
    ea0110p228
  - X-linked hypophosphatemic rickets and FGF23 levels: the importance of a correct reference range
    
    ea0110p229
  - Getting bone health right from the start: new tools for bone mineral density evaluation and determinants of BMD from pregnancy to 12 months of life
    
    ea0110p230
  - Genotype-phenotype insights and longitudinal outcomes in WNT1-related osteogenesis imperfecta type XV: a 14-year study of 44 chinese patients
    
    ea0110p231
  - Increased MMP13-bip interaction and activated ER stress contribute to SEMD in patient-ipsc-derived chondrogenic with MMP13 variant
    
    ea0110p232
  - Non-interventional post-authorisation safety study of burosumab in the treatment of children and adolescents with X-linked hypophosphataemia: second interim analysis
    
    ea0110p233
  - CALIBRATE-PEDS: a phase 2/3, multicenter, single-arm study evaluating the pharmacokinetics, efficacy, and safety of encaleret in pediatric participants with autosomal dominant hypocalcemia type 1
    
    ea0110p234
  - Triptorelin effects on linear growth and bone mineral density in transgender adolescents: a longitudinal study
    
    ea0110p235
  - Vitamin D supplementation during pregnancy does not improve maternal bone mineral density at 4 years post-partum
    
    ea0110p236
  - Characterization of bone density, strength, and mineral metabolism in 20 adults with monoallelic ENPP1 pathogenic variants
    
    ea0110p237
  - Estimating the risk of chronic kidney disease progression in chronic hypoparathyroidism: a retrospective matched cohort study, using real world data from England
    
    ea0110p238
  - Evaluation of ALP and PLP as a screening tool for ALPL mutations in hypophosphatasia: a study in chinese pediatric patients
    
    ea0110p239
  - Renal safety of zoledronic acid infusion in osteoporosis patients: a retrospective analysis
    
    ea0110p240
  - Real-world bone health outcomes in surgical, medical, and monitored patients with primary hyperparathyroidism
    
    ea0110p241
  - Exploring parathyroid carcinoma: clinical and pathological observations from a two-decade review
    
    ea0110p242
  - Obesity and blunted FGF23 response associate with kidney impairment in patients with hypoparathyroidism
    
    ea0110p243
  - Effects of different dietary patterns on bone health: mouse models
    
    ea0110p244
  - Efficacy of anastrozole in adolescent boys with limited growth potential: a retrospective analysis
    
    ea0110p245
  - Atypical parathyroid tumor in patients with primary hyperparathyroidism: predictive preoperative characteristics
    
    ea0110p246
  - Does an aggressive onset affect prognosis? insights into atypical parathyroid tumors
    
    ea0110p247
  - Tumour induced osteomalacia in a teenager: successful tumour localisation (68-Ga DOTATE PET-CT), tumour genetics (FGFR1 fusion gene) and tumour removal
    
    ea0110p248
  - Pathways to facilitate early recognition and diagnosis of hypochondroplasia
    
    ea0110p249
  - The IMPACT survey: healthcare experiences reported by individuals with osteogenesis imperfecta and their caregivers
    
    ea0110p250
  - A case of heterozygous PTHLH deletion causing brachydactyly type E2
    
    ea0110p251
  - Insufficient bone mineralization to sustain mechanical load of weight in obese girls: a cross-sectional study
    
    ea0110p252
  - Clinical significance of chloride-to-phosphorus and chloride-to-magnesium ratios in primary hyperparathyroidism
    
    ea0110p253
  - Phenotypic heterogeneity and long-term bisphosphonate outcomes in osteogenesis imperfecta type V: an 8-year retrospective study of 143 chinese patients
    
    ea0110p254
  - Solving pancreatic insufficiency as a clue to normal vitamin D serum concentrations in cystic fibrosis
    
    ea0110p255
  - Predictors of long-term morbidity and mortality in patients with chronic post-surgical hypoparathyroidism
    
    ea0110p256
  - Effective management of rebound hypercalcemia during denosumab therapy in pediatric osteogenesis imperfecta through individualized calcium supplementation
    
    ea0110p257
  - The significance of gender regarding the effects of primary hyperparathyroidism on the cardiometabolic profile of the patients: a single-center experience
    
    ea0110p258
  - Histological and laboratory factors associated with negative 99mtc-sestamibi scintigraphy in primary hyperparathyroidism: insights from a retrospective analysis
    
    ea0110p259
  - The complex link between obesity and bone mineral density: exploring the role of body composition
    
    ea0110p260
  - The diagnostic incidence of normocalcaemic hyperparathyroidism decreases and diagnostic concordance of parathyroid hormone (PTH) assays improves with assay- and age-specific PTH reference intervals
    
    ea0110p261
  - Profile of patients initiating abaloparatide treatment
    
    ea0110p262
  - Birth outcomes and educational level among patients with post-surgical and non-surgical hypoparathyroidism
    
    ea0110p263
  - Bone phenotype in infantile hypercalcemia-1 caused by CYP24a1 pathogenic variant
    
    ea0110p264
  - Pseudohypoparathyroidism type 1b diagnosed in adulthood: a novel family deletion in the GNAS locus
    
    ea0110p265
  - The united kingdom adult northstar network consensus recommendation of management of osteoporosis in adults with duchenne muscular dystrophy and transition to adult care
    
    ea0110p266
  - Vitamin d-dependent rickets type 2a in a 1-year-old girl: a rare case of alopecia and hypocalcemic jerking episodes
    
    ea0110p267
  - Design of the ACCEL study: a prospective clinical assessment study in children with hypochondroplasia
    
    ea0110p268
  - The impact of parathyroid adenoma removal on the quality of life of patients with primary hyperparathyroidism
    
    ea0110p269
  - Denosumab treatment of two children with inoperable spinal aneurysmal bone cysts
    
    ea0110p270
  - Bone mineralization in children aged 7-10 years born after assisted reproductive technology with frozen and fresh embryo transfer
    
    ea0110p271
  - Machine learning model on opportunistic computed tomography for predicting vertebral fracture risk in women undergoing hormone deprivation therapy for breast cancer
    
    ea0110p272
  - Nonsurgical hypoparathyroidism: insights from a single-center experience
    
    ea0110p273
  - Association of size at birth and bone mineral density in adolescents
    
    ea0110p274
  - Hypertension in primary hyperparathyroidism: predictive factors and post-parathyroidectomy outcomes
    
    ea0110p275
  - Years later: cracking the mystery of x-linked hypophosphatemic rickets
    
    ea0110p276
  - Pediatric parathyroid adenomas: a single tertiary care center experience
    
    ea0110p277
  - Patient-reported outcomes and quality of life in children and adults with hpp treated with asfotase alfa
    
    ea0110p278
  - Hospitalizations in people with rare bone diseases across age groups: a population-based cohort study in switzerland
    
    ea0110p279
  - Clinical features of pediatric hypophosphatasia and eight-year outcomes of enzyme replacement therapy in korea
    
    ea0110p280
  - Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome
    
    ea0110p281
  - Genotype-phenotype correlations and therapeutic outcomes in osteogenesis imperfecta type vi: an 11. 5-year cohort study of 36 chinese pediatric patients
    
    ea0110p282
  - Onset of puberty in achondroplasia
    
    ea0110p283
  - Diabetes mellitus marginally impairs bone quality with chronic kidney disease
    
    ea0110p284
  - Biochemical response kinetics in vitamin d resistant rickets (VDDR) type 1 and 2: 13-year retrospective analysis from a tertiary care centre
    
    ea0110p285
  - Severe short stature secondary to distal renal tubular acidosis with slc4a1 gene mutation in a nigerian adolescent
    
    ea0110p286
  - Localization imaging and postoperative outcomes in primary hiperparathyroidism (phpt): is less enough?
    
    ea0110p287
  - Management of osteoporosis in a pediatric case of severe osteolysis
    
    ea0110p288
  - Hereditary and acquired phosphopenic rickets: from childhood to adulthood
    
    ea0110p289
  - Parathyroid washout's role in accurate adenoma localisation and diagnostic cut-offs
    
    ea0110p290
  - Pubertal development in hypophosphatemic rickets: does it have an impact on growth?
    
    ea0110p291
  - Pregnancy management in ectonucleotide pyrophosphatase/phosphodiesterase family member 1 (ENPP1) deficiency: a case report and considerations for maternal medicine care
    
    ea0110p292
  - "Familial hypocalciuric hypercalcemia in adolescence: diagnostic challenges and the role of genetic testing"
    
    ea0110p293
  - "A diagnostic odyssey: camurati - engelmann syndrome presenting as childhood onset leg pains and stiffness"
    
    ea0110p294
  - Bone health index (BHI) in children with osteogenesis imperfecta: is it an accurate tool for predicting fracture risk?
    
    ea0110p295
  - Clinical and laboratory characteristics of genetic rickets: a single-center experience with long-term outcomes
    
    ea0110p296
  - A novel case of macroprolactinoma in a patient with phenylketonuria
    
    ea0110p297
  - Trabecular bone score and risk of vertebral fracture in systemic lupus erythematosus children and adolescent who treated with glucocorticoids
    
    ea0110p298
  - Hypercalcaemia from primary hyperparathyroidism and CYP24a1 pathogenic variant: a coincidence or an underlying mechanism?
    
    ea0110p299
  - Effect of long-term treatment with teriparatide and vitamin k on bone density and bone markers, glucose metabolism and body composition in severe osteoporotic patients
    
    ea0110p300
  - Prevention and treatment of hypocalcaemia in children undergoing total thyroidectomy
    
    ea0110p301
  - X-linked hypophosphatemic rickets in children and adolescents - single centre expertise in romania
    
    ea0110p302
  - From highs to lows: the challenge of hypocalcemia after parathyroid carcinoma surgery
    
    ea0110p303
  - Biochemical ratios for predicting primary hyperparathyroidism: revisiting simple yet powerful diagnostic tools
    
    ea0110p304
  - Bone marrow stem cells derived exosomes for osteoporosis treatment
    
    ea0110p305
  - Jaw tumor syndrome: a rare endocrine disorder with diverse clinical manifestations
    
    ea0110p306
  - Heterozygous WNT1 variant causing severe, adult-onset hereditary osteoporosis
    
    ea0110p307
  - Infantile idiopathic hypercalcemia associated with heterozygous mutation of SLC34A1: a case series
    
    ea0110p308
  - Analysis of symptoms in paediatric patients with familial hypocalciuric hypercalcaemia, a case series
    
    ea0110p309
- Diabetes and Insulin
- - Secretagogin deficiency leads to gut microbiome dysbiosis and impairs thermogenesis in age-related diabetes via reduced 12,13-diHOME
    
    ea0110p7
  - Diabetes type 1 can induce testicular atrophy with Leydig cell hyperplasia and germ cell depletion and therefore negatively influence reproductive function in rats
    
    ea0110p8
  - Assessment of metabolic status in adolescents with type 1 diabetes: the utility of the SPISE index
    
    ea0110p9
  - Long-term beta-cell function and GLP-1 secretion after sleeve gastrectomy vs gastric bypass in patients with type 2 diabetes: the oseberg clinical trial
    
    ea0110p310
  - Cathepsin s is elevated in pancreatic islets and plasma in new-onset type 1 diabetes and positively associates with systemic inflammatory cytokines
    
    ea0110p311
  - Challenges in managing MODY 12: a case report
    
    ea0110p312
  - Gut microbiota-derived indole-3-propionic acid alleviates diabetic kidney disease through its mitochondrial protective effect via reducing ubiquitination mediated-degradation of SIRT1
    
    ea0110p314
  - Leukocyte telomere length as a potential indicator of early kidney dysfunction in persons with type 2 diabetes
    
    ea0110p315
  - Effect of semaglutide vs placebo on HbA1c, weight, mental health and SF-36: a randomized clinical trial in people with pre-diabetes, obesity and schizophrenia
    
    ea0110p316
  - Cardiorespiratory fitness and cardiovascular risk in youth with type 1 diabetes
    
    ea0110p317
  - Parental perception on immunotherapy for children at risk of type 1 diabetes and islet cell transplantation/stem cell therapy for children with type 1 diabetes
    
    ea0110p318
  - Can diabetes self-management applications replace continuous glucose monitoring in low-resource environments?"
    
    ea0110p320
  - Comparison of moderate intensity atorvastatin and ezetimibe with high intensity atorvastatin on cardiovascular events and diabetes in patients with angina pectoris
    
    ea0110p321
  - To study the effect of medical nutrition therapy on school-time hyperglycemia and the glycemic outcomes in childeren with type 1 diabetes mellitus
    
    ea0110p322
  - The impact of regulatory-approved and open-source automated insulin delivery systems on glycemic control: real-world data from a heterogeneous population
    
    ea0110p323
  - Can insulin level measured by oral glucose tolerance test be a guide in the diagnosis of prediabetes?
    
    ea0110p324
  - HDL Lipidome remodeling is linked to diabetic kidney disease progression independent of albuminuria severity
    
    ea0110p325
  - Relevance of PFKP lysine lactylation in coupling glycolytic adaptation and mitochondrial respiration in diabetic proximal tubules
    
    ea0110p326
  - Alpelisib therapy for patients with congenital hyperinsulinism
    
    ea0110p327
  - Hyperinsulinemic hypoglycaemia in small for gestational age neonates: clinical characteristics, biochemical features, treatment, and clinical outcome
    
    ea0110p328
  - Predictive markers of insulin resistance and dysglycemia in children and adolescents with overweight or obesity before and after the COVID-19 pandemic
    
    ea0110p329
  - Co-designing a multicentre quality improvement initiative for hypoglycaemia: the dekode model
    
    ea0110p330
  - Prevalence of MASLD in children and adolescents with type 1 diabetes assessed by transient elastography
    
    ea0110p331
  - Portosystemic shunt as a cause of alternating ketotic hypoglycemia and hyperinsulinism in patients with associated anomalies
    
    ea0110p332
  - Disparities in diabetes incidence and prevalence among koreans under 30 in 2008-2021: a greater burden on socioeconomically disadvantaged populations
    
    ea0110p333
  - Influence of SARS-CoV-2 virus and COVID-19 pandemic on course of type 1 diabetes in children during the first year of disease
    
    ea0110p334
  - Correlation between visceral fat and estimated disposal glucose rate in patients with type 1 diabetes
    
    ea0110p335
  - Screening of first-degree relatives of children with type 1 diabetes: preliminary results
    
    ea0110p336
  - [ldquo]Urinary c-peptide to creatinine ratio (UCPCR) as a marker of insulin secretion: impact of glucose load and sex differences[rdquo]
    
    ea0110p338
  - Single-cell analysis reveals plasticity of pancreatic [beta]-cells during pregnancy and postpartum in mice
    
    ea0110p339
  - Influenza vaccine coverage and factors associated with vaccination in adults with type 1 diabetes - a danish register-based study
    
    ea0110p340
  - Continuous glucose monitoring in paediatric residents with normal glucose metabolism: correlations to 24-hour duty schedule
    
    ea0110p341
  - Acceptance of artificial intelligence by clinicians: a study on adoption and integration in medical practice
    
    ea0110p342
  - Postprandial glucose response to a novel low-sucrose chocolate spread in adults with type 1 diabetes: a randomized, double-blinded, cross-over, controlled trial
    
    ea0110p343
  - Advance glycation end-products in diabetic persons with and without retinopathy during the first and second year of the project EEA-RESEARCH-60 [ldquo]perdire[rdquo]
    
    ea0110p344
  - Randomized controlled trial on the effectiveness and usability of interactive diabetes management application: a multi-centre study
    
    ea0110p345
  - JAK/STAT and TRAIL signaling in latent autoimmune diabetes in adults: findings from single-cell transcriptomics
    
    ea0110p346
  - Assessment of insulin-releasing and glucose-lowering effects of Piper guineense extracts in cellular and animal models of type 2 diabetes
    
    ea0110p347
  - Liver androgen receptor knockout fails to prevent high-fructose diet-induced glucose dysregulation in female mice
    
    ea0110p348
  - Experience with the use of dapagliflozin in patients with ckd of various etiologies
    
    ea0110p349
  - Accuracy and cost saving using haemoglobin A1c and lipid profiles point-of-care testing: a multicentre study
    
    ea0110p350
  - CGM as a useful tool providing deeper insights into the glucose metabolism of patients with transfusion dependent b-thalassemia
    
    ea0110p351
  - KARLOTTA 2. 0 (kids + adolescents research learning on tablet teaching aachen) - study results of a digital educational app for pediatric patients with type 1 diabetes
    
    ea0110p352
  - Incidence trends and seasonal variation of new cases of type 1 diabetes in lithuanian children in 2001-2022
    
    ea0110p353
  - Pilot screening program for early detection of type 1 diabetes in first-degree relatives in saudi arabia (VISION-T1D)
    
    ea0110p354
  - Impact of sex and BMI on A1C trajectory amongst children and adolescents with type 1 diabetes
    
    ea0110p355
  - Incidence and burden of childhood diabetes in china from 1990 to 2021: findings from the global burden of disease study 2021
    
    ea0110p356
  - Elevated alanine aminotransferase predicts the risk of prediabetes/diabetes and NAFLD in obese children: a cross-sectional retrospective study
    
    ea0110p357
  - Giving the child with diabetes a clear voice: what matters the most to children with type 1 diabetes attending a pediatric diabetes clinic? A substudy in the ProKidsDia project
    
    ea0110p358
  - Use of portable elastomeric pump for home-based continuous enteral carbohydrate administration through gastrostomy in children with congenital hyperinsulinism or ketotic hypoglycemia
    
    ea0110p359
  - Association of the triglyceride/HDL cholesterol ratio with cholesterol efflux in adolescents with type 2 diabetes mellitus
    
    ea0110p361
  - Effects of transition from basal insulin glargine 100 u/ml to 300 u/ml on glycemic control in children and adolescents with type 1 diabetes - real-world data
    
    ea0110p362
  - Early detection of peripheral and autonomic neuropathy in children and adolescents with type 1 diabetes mellitus
    
    ea0110p363
  - Does celiac disease have an impact on hypoglycemia awareness in children with type 1 diabetes?
    
    ea0110p364
  - Prognostic value of the neutrophil-to-lymphocyte ratio for acute appendicitis in children with acute abdominal pain and T1DM
    
    ea0110p365
  - Beyond glycemic control: managing rare complications in type 1 diabetes
    
    ea0110p366
  - The interplay of cortisol, trygliceride glucose index and microalbuminuria in type 2 diabetes: a prospective observational case-control study
    
    ea0110p367
  - Unveiling the spectrum of mitochondrial diabetes - a single center, multidisciplinary case series analysis
    
    ea0110p368
  - Diabetic foot recurrence: a study of predictive factors
    
    ea0110p369
  - Simulation-based education enhances healthcare professionals' confidence in managing acute diabetes scenarios
    
    ea0110p370
  - Development and validation of hba1c prediction models using CGM metrics in korean pediatric patients with type 1 diabetes: insights on average glucose and recent glycemic trends of CGM
    
    ea0110p371
  - Challenges in transitioning from pediatric to adult diabetes care in armenia: patient experiences and systemic gaps
    
    ea0110p372
  - New criteria of 1-hour post-load plasma glucose for the diagnosis of intermediate hyperglycaemia and type 2 diabetes in adolescents
    
    ea0110p373
  - Causal association between diabetes and herpesvirus infections: a bidirectional two-sample mendelian randomization study
    
    ea0110p374
  - Epidemiology of monogenic diabetes in the czech republic
    
    ea0110p375
  - Closed-loop CamAPS system shows time-specific glucose variability and hypoglycemic patterns in very young children with type 1 diabetes
    
    ea0110p376
  - Comprehensive genetic testing reveals a deep intronic variant in HNF1A in a family with early-onset diabetes mellitus
    
    ea0110p377
  - Cross sectional and longitudinal study of arterial stiffness in pediatric patients with type 1 diabetes mellitus (T1DM), with glycemic metrics derived from continuous glucose monitoring (CGM) devices
    
    ea0110p378
  - Development and validation of diabetes interpreter, a mobile application-based tool for point-of-care evaluation of children with diabetes
    
    ea0110p379
  - Fibrosis and severe steatosis contribute to liver dysfunction in patients with insulin resistance after hematopoietic stem cell transplantation
    
    ea0110p380
  - Three-year OCT/OCTA follow-up of retinal neurovasculature in pediatric type 1 diabetes
    
    ea0110p381
  - Factors affecting caregiver burden in families of children with type 1 diabetes
    
    ea0110p382
  - Omnipod5 real-world data from the first paediatric users universal coverage under the united kingdom national health service
    
    ea0110p383
  - Navigating complexity and challenges in managing type 1 diabetes in children with neurodiverse diagnoses - a qualitative study
    
    ea0110p384
  - A longitudinal analysis of the impact of alarmed sensors on anxiety, depression, sleep quality, quality of life and treatment satisfaction in patients with type 1 diabetes
    
    ea0110p385
  - The trend in hospitalizations for diabetes mellitus in brazilian children under 10 years of age: an analysis from 2013 to 2023
    
    ea0110p386
  - A novel GCK gene variant causing juvenile-onset adult-type diabetes in a family is reported for the first time
    
    ea0110p387
  - Depressive symptoms in youths with diabetes mellitus and their associating factors: an observational study in a single centre in hong kong
    
    ea0110p388
  - Twenty-four hours glycemic profile of women with early gestational diabetes mellitus
    
    ea0110p389
  - Association between serum lipid profile and glycemic control in adolescents with newly diagnosed type 2 diabetes: a single center study
    
    ea0110p390
  - Fasting blood glucose as predictor in achieving glycemic control among patients with gestational diabetes mellitus on non-pharmacologic therapy: a retrospective cohort study
    
    ea0110p391
  - Association between genetic variants of SLC30A8, CDKAL1 and HHEX and increased risk of gestational diabetes mellitus: implications for early detection and personalized management
    
    ea0110p392
  - Performance of an algorithms predicting mortality in medical vs surgical patient with diabetes
    
    ea0110p393
  - Weight stigma in pediatric type 1 diabetes: evaluating patient level factors and diabetes related outcomes
    
    ea0110p394
  - Levels of antioxidants and oxidizing agents in patients with different types of diabetes mellitus - a serum biomarker assessment
    
    ea0110p395
  - Efficacy of frequency rhythmic electrical modulated system (FREMS) in the treatment of diabetic neuropathy: a systematic review and meta-analysis of randomized controlled trials
    
    ea0110p396
  - Anti-parietal cell antibodies prevalence and clinical implications in youths with type 1 diabetes
    
    ea0110p397
  - Seasonal trends, clinical characteristics, and glycemic control in type 1 diabetes mellitus: a descriptive study from two private tertiary hospitals in nairobi, Kenya
    
    ea0110p398
  - Exploring the early symptoms of depression in children, adolescent and young adults: a review with public patient involvement
    
    ea0110p399
  - A rare metabolic puzzle: the case of an infant with hadh mutation
    
    ea0110p400
  - Morphofunctional assessment in type 1 diabetes mellitus: usefulness of muscle ultrasound in the evaluation of body composition and its relationship with metabolic variables
    
    ea0110p401
  - Pancreatic steatosis in newly diagnosed type 2 diabetes: relationships with glycemic control and exocrine function
    
    ea0110p402
  - Neonatal diabetes: clinical characteristics, genetic analysis and long-term follow-up from a single-center experience
    
    ea0110p403
  - Comparative analysis of ventricular repolarization in patients with type 1 diabetes vs. control and patients using insulin pump vs. multiple daily injections
    
    ea0110p404
  - Investigation of the relationship between alexisomia and treatment adherence in diabetic obese individuals: a pilot study
    
    ea0110p405
  - Clinical characteristics, risk factors, and outcomes of DKA in type 1 diabetes: a comparative study of continuous subcutaneous insulin infusion (CSII) vs multiple daily injections (MDI)
    
    ea0110p406
  - Association of arterial stiffness with mineral metabolism in type 2 diabetes patients with chronic kidney disease
    
    ea0110p407
  - Functional analysis of RFX2 gene as a candidate gene for monogenic diabetes
    
    ea0110p408
  - Three case studies of congenital hyperinsulinism - variants and clinical outcomes
    
    ea0110p409
  - Multi-center investigation of pediatric diabetes in China
    
    ea0110p410
  - Therapeutic education in children and adolescents with type 1 diabetes mellitus; systematic review
    
    ea0110p411
  - Hamman's syndrome as a rare complication of diabetic ketoacidosis in a newly diagnosed pediatric patient with type 1 diabetes mellitus
    
    ea0110p412
  - Multidisciplinary team transition model of care for type 1 diabetes: health outcomes after 2 years of implementation
    
    ea0110p413
  - Correlation between inflammation, metabolic syndrom and visceral fat in young type 1 diabetes patients
    
    ea0110p414
  - Can c-peptide/glucose ratio at the diagnosis be a marker for predicting short or long term metabolic control in type 1 diabetes?
    
    ea0110p415
  - Alpelisib associated hyperglycemia in patients with advanced breast cancer
    
    ea0110p416
  - Understanding severe hypoglycaemia in diabetes mellitus: a retrospective analysis into risk factors, management and outcomes
    
    ea0110p417
  - Real-world evidence of the effect of adjunctive semaglutide on weight change, liver steatosis and metabolic control in people with type 1 diabetes
    
    ea0110p418
  - Prevalence and characteristics of patients with cystic fibrosis-related diabetes in croatia
    
    ea0110p419
  - Partitioning the genetic risk of obesity and type 2 diabetes using single-cell multi-omics of the gastrointestinal tract
    
    ea0110p420
  - A proof-of-concept study of type 2 diabetes remission with pharmacotherapy
    
    ea0110p421
  - Type 1 diabetes children with less sleeping time have higher HbA1c level and shorter stature
    
    ea0110p422
  - Predictive factors of type 2 diabetes and prediabetes diagnosis in women with gestational diabetes
    
    ea0110p423
  - Using the telegram bot for differential diagnosis of diabetes mellitus and risk assessment of its complications
    
    ea0110p424
  - An unusual case of MODY
    
    ea0110p425
  - Exploring a synergistic approach: dual GLP-1 agonist combined with degludec basal insulin for early type 1 diabetes treatment and its impact on albumin-insulin producing cells expression
    
    ea0110p427
  - Comparative study on clinical indicators of type 1 diabetes mellitus in children in southwest china before and after the COVID-19 pandemic
    
    ea0110p428
  - Socioeconomic status, modifiable factors, and risk of microvascular complications in individuals with type 2 diabetes: a cohort study from the UK biobank
    
    ea0110p429
  - Challenges in the diabetes transition clinic: a 10-year experience at a tertiary care hospital
    
    ea0110p430
  - Evaluation of emergency department admission reasons and associated factors in pediatric patients diagnosed with type 1 diabetes mellitus
    
    ea0110p431
  - Investigation of lower urinary tract symptoms and their effects on quality of life in patients using sglt-2 (sodium-glucose cotransporter-2) inhibitors
    
    ea0110p432
  - Comparison of metabolic control in children with type 1 diabetes using reimbursed, self-funded intermittent, and self-funded continuous CGM
    
    ea0110p433
  - An Unusual case of late-onset ipex syndrome
    
    ea0110p434
  - Transforming youth diabetes care: the role of tellmi in providing digital mental health support in NHS somerset UK
    
    ea0110p435
  - The relationship of iron homeostasis and biochemical biomarkers according to therapeutic management in patients with type 2 diabetes
    
    ea0110p436
  - Monogenic diabetes: results from targeted sequencing in lithuania during 2017-2022
    
    ea0110p437
  - Maturity-onset diabetes of the young type 10 with a rare insulin gene mutation in a 35-year-old male
    
    ea0110p438
  - The association between metabolic score for insulin resistance and acanthosis nigricans in overweight and obese individuals: a cross-sectional study
    
    ea0110p439
  - Time in tight range during ramadan intermittent fasting in adolescents and young adults with diabetes: are the new CGM targets met?
    
    ea0110p440
  - Phenotypic variation of fasting glucose in GCK-related hyperglycaemia
    
    ea0110p441
  - Glycemic control in people living with type 1 diabetes using the medtronic minimed™ 780 system: results from the galaxy service in greece
    
    ea0110p442
  - Application of an extended NGS gene panel in 573 monogenic diabetes mellitus referrals
    
    ea0110p443
  - Body composition in T1DM: a comparison of patients using advanced hybrid closed-loop systems vs. multiple daily injections/patch pumps
    
    ea0110p444
  - Exploring pancreatic diabetes: key features and diagnostic insights from 145 patients
    
    ea0110p445
  - Renoprotective effects of dipeptidyl peptidase-4 inhibitors in diabetic kidney disease: a meta-analysis of randomized controlled trials
    
    ea0110p446
  - Subcutaneous insulin aspart in treatment of children with mild and moderate diabetic ketoacidosis
    
    ea0110p448
  - Characteristics of maturity-onset diabetes of the young: a single-center experience from a tertiary referral hospital
    
    ea0110p449
  - Progression and outcomes of prediabetes in children and adolescents: insights from an indian perspective
    
    ea0110p450
  - From pediatric to adult diabetes care: experience of the organized transition process of youth with type 1 diabetes
    
    ea0110p451
  - Evaluation of the performance of continuous glucose monitoring in the treatment of patients with congenital hyperinsulinism
    
    ea0110p452
  - Turning back the metabolic disturbances - results of treating two brothers with Berardinelli Seip syndrome with leptin analogue for five months
    
    ea0110p453
  - Driving data-driven impact through digital innovation: a collaborative case study between action4diabetes and correlaid's data4good initiatives
    
    ea0110p454
  - SGLT-2 Inhibitor-induced erythrocytosis and risk of coronary artery disease in type 2 diabetes - a nationwide cohort study
    
    ea0110p455
- Endocrine Related Cancer
- - Validation of prognostic biomarkers in adrenocortical carcinoma through a Next-Generation Sequencing in real-life setting
    
    ea0110p10
  - ACCacia, a novel machine-learning approach for adrenocortical carcinomas molecular classification in routine care
    
    ea0110p11
  - Measurement of circulating cell-free DNA concentrations for differential diagnosis of adrenal masses: a pilot study
    
    ea0110p12
  - Quantitative analysis of [¹⁸F]fluorocholine-PET acquisition times in patients with histopathologically proven primary hyperparathyroidism
    
    ea0110p456
  - Evolution of small (=4 cm) adrenal lesions diagnosed as adrenocortical carcinomas: a5 multicenter retrospective cohort study
    
    ea0110p458
  - Plasma concentrations of selected growth factors as a potential tool for detecting recurrence in endocrine tumors - a pilot study
    
    ea0110p459
  - Molecular characterization of circulating tumor cells (CTCs) in sporadic medullary thyroid carcinoma (spMTC) patients
    
    ea0110p460
  - Years of pediatric thyroid cancer experience at a tertiary care center
    
    ea0110p461
  - Exploring SDHA variants: navigating predisposition and incidental findings
    
    ea0110p462
  - Variable redifferentiation effect of larotrectinib for NTRK fusion-positive pediatric papillary thyroid carcinoma and disease outcomes off therapy
    
    ea0110p463
  - Radiogenomics pilot study in adrenocortical carcinoma: assessing the relationship between genetic background and computerized tomography texture
    
    ea0110p464
  - Increased serum visfatin in neuroendocrine tumors shows promise as a diagnostic biomarker: a single-center, cross-sectional study
    
    ea0110p465
  - A comparison of clinical and hormonal characteristics in patients with paraneoplastic cushing's syndrome and in those with cushing's disease
    
    ea0110p466
  - Long-term persistence of glycemic dysregulation in patients with a history of pheochromocytoma/paraganglioma
    
    ea0110p467
  - [⁶⁸Ga]Ga-DOTA-exendin-4 PET/CT for the localization of insulinoma: results of an international, dual-center, retrospective, open-label real-world imaging study
    
    ea0110p468
  - Phenotypic and genotypic characteristics of patients with MEN2 in france: preliminary features from the MEN2 french database
    
    ea0110p469
  - Individual dosimetry in radionuclide therapy (RLT) of NET using [177Lu]Lu-DOTA-TATE or [177Lu/90Y]-DOTA-TATE mixture - effect on total administered RLT activity
    
    ea0110p470
  - Thyroid carcinoma in children and adolescents - subtypes and clinical evolution
    
    ea0110p471
  - Annual tumour surveillance screening for paediatric carriers of SDHX gene variants in family clinics at barts health NHS trust
    
    ea0110p472
  - USP10 as a multifaceted therapeutic target in adrenocortical tumors: implications for tumor biology and steroidogenesis
    
    ea0110p473
  - Pediatric and adolescent von hippel-lindau disease: tumor profiles, genotype-phenotype correlations, and a comparison with adults
    
    ea0110p474
  - Treatment of lung neuroendocrine tumors with ¹⁷⁷Lu-DOTATATE: experience from a tertiary oncology centre
    
    ea0110p475
  - MiR-191-5p represents a potential personalized diagnostic and therapeutic tool in the pathophysiological interplay between obesity and prostate cancer
    
    ea0110p476
  - DICER1 syndrome: clinical and endocrinological manifestations in pediatric patients followed in a third-level hospital
    
    ea0110p477
  - Frequency and phenotypic spectrum of DICER1 syndrome among children and adolescents with thyroid cancer
    
    ea0110p478
  - Cabozantinib in advanced adrenocortical carcinoma - first preliminary results of the prospective phase II caboACC study
    
    ea0110p479
  - Rare occurrence of thyroid paraganglioma in the context of SDHB mutation: a case report
    
    ea0110p480
  - Chromogranin a and pancreatic polypeptide are not suitable for the screening of pancreatic neuroendocrine tumors in MEN1 - a long-term follow-up study
    
    ea0110p481
  - Ectopic adrenocorticotrophic hormone secreting bronchial carcinoid: a retrospective study from a tertiary center
    
    ea0110p482
  - Medullary thyroid carcinoma and c-cell hyperplasia in patients affected with neurofibromatosis type 1
    
    ea0110p483
  - Thyroid and pituitary dysfunction after total body irradiation as conditioning therapy of haematopoietic stem cell transplantation during childhood
    
    ea0110p484
  - Pediatric papillary thyroid carcinoma as the first manifestation of undiagnosed hereditary tumor predisposition syndrome?
    
    ea0110p485
  - The importance of assessing IDO1 activity when targeting tryptophanyl-tRNA synthetase (WARS) inhibition in medullary thyroid carcinoma (MTC)
    
    ea0110p486
  - Lipodystrophy in children following hematopoietic stem cell transplantation: analysis of prevalence, risk factors and response to conventional treatments
    
    ea0110p487
  - Unraveling the role of autophagy in adrenocortical carcinoma
    
    ea0110p488
  - Urinary steroid profiling by GC-MS as a diagnostic tool for evaluating malignancy of adrenocortical tumors - profile fit for purpose?
    
    ea0110p489
  - Exploration of the genomic clinical correlations of follicular differentiated thyroid cancer through a 56 gene panel next generation sequencing study
    
    ea0110p490
  - Clinical implications of measuring muscle mass by computed tomography in neuroendocrine tumor patients
    
    ea0110p491
  - Selective early genetic screening for targetable gene fusions in papillary thyroid cancer (PTC) tissues
    
    ea0110p492
  - Identifying the burden of hypothalamic syndrome in paediatric patients with craniopharyngioma in a single specialised centre cohort
    
    ea0110p493
  - Multiple endocrine neoplasia 2B in two siblings with short stature, an uncommon association
    
    ea0110p494
  - Serum and cerebrospinal fluid hCG leves in children with beta hCG producing germ cell tumors
    
    ea0110p495
  - Prevalence and morphology of pineal gland calcifications in children with cranial germ cell tumors are different from normal chidren aged 0-15 years
    
    ea0110p496
  - Co-occurrence of burkitt lymphoma and follicular thyroid adenoma in a pediatric patient: a rare case report
    
    ea0110p498
  - Overweight and obesity in survivors of pediatric brain tumor
    
    ea0110p499
  - Treatment with GnRH analogues in paediatric and adolescent patients with cancer diagnosis undergoing chemotherapy
    
    ea0110p500
  - Genomic view of poorly diffentiated thyroid cancer as a bridge between well differentiated and anaplastic thyroid cancer
    
    ea0110p501
  - Menin expression in parathyroid tumors of patients with multiple endocrine neoplasia type 1 phenocopies
    
    ea0110p502
  - Targeted management of recurrent paraganglioma with SDH-B mutation: a case report
    
    ea0110p503
  - Thyroid core-needle biopsy. the first 569 results in Romania
    
    ea0110p504
  - Periprostatic adipose tissue (PPATs) adipokine profile highlights lipocalin-2 as a potential key player in the pathophysiological association between PPAT, obesity and prostate cancer microenvironment
    
    ea0110p505
  - Clinical, hormonal, and neuroradiological characteristics and therapeutic outcomes of prolactinomas in children and adolescents at a single center
    
    ea0110p506
  - Severe hypercalcemia in an infant caused by PTHrP secretion from renal malignancy
    
    ea0110p507
  - Premature pubarche in 20 month old girl as a first sign of Li-Fraumeni syndrome - case report
    
    ea0110p508
  - Challenges in the diagnosis of patients with mild and moderate hypercalcitoninemia and nontoxic multinodular goiter
    
    ea0110p509
  - Redifferentiation treatment in radioiodine refractory metastatic papillary thyroid cancer
    
    ea0110p510
  - The metastatic medullary thyroid carcinoma: a rare cause of ectopic ACTH-dependent cushing's syndrome
    
    ea0110p511
  - Management of ectopic cushing's syndrome: a retrospective analysis of therapeutic outcomes
    
    ea0110p512
  - The impact of 12 months of aromatase inhibitors on body composition in postmenopausal women with early-stage breast cancer
    
    ea0110p513
  - Extraordinary cortisol and 11-deoxycorticosterone co-secretion from an ectopic peritoneal adrenocortical carcinoma
    
    ea0110p514
  - Patient reported outcome measurements (PROM) for the evaluation of the psychosomatic status in patients with adrenocortical carcinoma
    
    ea0110p515
  - Endocrine toxicity constitutes an independent predictor of survival in patients with extensive stage small cell lung cancer
    
    ea0110p516
  - Six unrelated italian kindreds with multiple endocrine neoplasia type 4 (MEN4) harboring variants of the CDKN1B gene
    
    ea0110p517
  - Whole exome sequencing of gastroeneteropancreatic neuroendocrine tumors reveals specific SNV associated with epithelial-mesenchymal transition
    
    ea0110p518
  - Persistent severe hypokalemia as a critical marker of diagnosis and response to treatment in ectopic cushing's syndrome (ECS) caused by small-cell lung cancer (SCLC)
    
    ea0110p519
  - Liver transplantation in a patient with small-intestine neuroendocrine tumor (NET) and carcinoid syndrome
    
    ea0110p520
  - Thyroid nodule progression prediction using convolutional neural networks and ultrasound images
    
    ea0110p521
  - Bilateral phaeochromocytomas in a young patient with a pathogenic MAX gene variant
    
    ea0110p522
  - Cribriform morular carcinoma (CMC), a heterogeneous neoplasm of the thyroid gland. Report of four cases
    
    ea0110p523
  - Identifying vulnerable pituitary tumor patient subgroups after endoscopic transsphenoidal surgery: a prospective study on psychological well-being and self-perceived health
    
    ea0110p524
  - Comparative evaluation of postoperative pathology in patients with fine needle aspiration biopsy cytology of bethesda category IV
    
    ea0110p525
  - Unravelling thermotolerance in adrenocortical carcinoma: implications for hyperthermia-based therapies
    
    ea0110p526
  - Diagnostic and therapeutic specificity of thyroid nodules in children
    
    ea0110p527
  - Intracranial germ cell tumors presenting with precocious puberty and diabetes insipidus in female patients: three case reports
    
    ea0110p528
  - Adrenocortical carcinoma in a 9-year-old girl with li-fraumeni syndrome: a case report
    
    ea0110p529
  - Association of hemizygous MAMLD1 gene mutation and testiculer germ cell neoplasia in situ: a case report
    
    ea0110p530
- Environmental Endocrinology
- - The effect of iodine- and selenium-fortified eggs on urinary excretion: findings from a randomized controlled study
    
    ea0110p13
  - Impact of early-life exposure to phthalates on anogenital distances in a cohort of healthy children and their mothers, from birth to three years of age
    
    ea0110p14
  - Plasma phthalate metabolites correlate with genetic alterations in PCOS patients with metabolic dysfunction
    
    ea0110p531
  - Longitudinal exposure to benzophenones, parabens, and simple phenolic substances in children and adolescents and effects on puberty
    
    ea0110p532
  - Higher pfas exposure associated with lower 24h urine aldosterone in pregnant women. the odense child cohort
    
    ea0110p533
  - Circadian temperatures in relation to thyroid function and cold exposure among subsistence hunters in east greenland
    
    ea0110p534
  - Endocrine disruption by phthalates and substitute substances: a hidden link to hypertension via adrenal steroidogenesis?
    
    ea0110p535
  - The impact of phthalates on adrenal steroidogenesis in HAC15 cells
    
    ea0110p536
  - Early-life exposure to phthalates and risk assessment in a cohort of healthy mother-infant dyads: a 3-year follow-up study
    
    ea0110p537
  - Exposure to per- and polyfluoroalkyl substances during fetal development and risk of testicular germ cell cancer in adult life
    
    ea0110p538
  - From sea to sample: tracing iodine nutrition in the faroe islands
    
    ea0110p539
  - Menopause related psychological symptoms influence work and careers more than vasomotor symptoms: findings from a cross-sectional study among 1562 women in diverse occupations
    
    ea0110p540
  - Awareness of endocrine disrupting chemicals among medical students and physicians: is it time for urgent curriculum and training reform?
    
    ea0110p541
  - Phthalates: an endocrine disrupting hazard from birth to adulthood
    
    ea0110p542
  - Final adult height in male patients with central precocious puberty after GnRH agonist treatment
    
    ea0110p543
  - Association between urinary 3-phenoxybenzoic acid and thyroid function among 6-year-old children according to iodine status
    
    ea0110p544
  - The LIFE-MILCH project: exposure to endocrine-disrupting chemicals in breast milk samples from the risk assessment model
    
    ea0110p545
  - An investigation of basic biochemical and endocrinological parameters in 34, 595 patients with occupational heavy metal exposure: a Turkey cohort
    
    ea0110p546
  - Triptorelin stimulated gonadotropin concentrations for precocious puberty
    
    ea0110p547
  - Sex-specific associations between maternal and postnatal exposure to bisphenol a (BPA) and children's body mass index: a prospective cohort study
    
    ea0110p548
- Fetal and Neonatal Endocrinology
- - Differential expression and protein abundance of key regulators of the IGF, adiponectin and PPAR signalling pathways in placentas from small, adequate and large for gestational age newborns
    
    ea0110p15
  - The pharmaceutical-grade oral Glyburide = Glibenclamide suspension, AMGLIDIA, is safe and efficacious in French patients with neonatal diabetes mellitus
    
    ea0110p16
  - Hypospadias and fetal growth restriction: a shared genetic origin?
    
    ea0110p549
  - Deciphering the physiological downregulation of mineralocorticoid receptor expression at birth: implications of mir-409-3p and mir-431-5p
    
    ea0110p551
  - Testing a continuous glucose monitoring assessment tool for congenital hyperinsulinism
    
    ea0110p552
  - MEN2B syndrome, the impossible clinical challenge and how genomic newborn screening will improve morbidity and mortality
    
    ea0110p553
  - Altered neuronal function and impaired cognition among healthy people with different cortisol levels based on resting-state fMRI analysis
    
    ea0110p554
  - Which algorithm for antenatal management of disorders/differences of sex development? PECAN-VDG retrospective study of lyon multidisciplinary prenatal diagnosis center experience
    
    ea0110p555
  - Impact of in utero exposure to sesamol on the folliculogenesis and metabolism in F1 female offspring rats
    
    ea0110p556
  - Hypoglycemia to hyperglycemia: the clinical spectrum of ABCC8 gene variants
    
    ea0110p557
  - Dasiglucagon treatment consistently reduces hypoglycemia assessed by continuous glucose monitoring in children with congenital hyperinsulinism across subgroups
    
    ea0110p558
  - Update on genetic etiology in vietnamese children with congenital hyperinsulinism during 15 years (2010-2024) at tertiary pediatric center
    
    ea0110p559
  - Collaborative global advocacy to improve the lives of children and families with congenital hyperinsulinism
    
    ea0110p560
  - Lower FT4 levels are associated with increased risk of C-section or assisted delivery
    
    ea0110p561
  - Prevalence and predictors of small for gestational age neonates and endocrinological follow-up: a retrospective analysis of 2018 birth cohort
    
    ea0110p562
- Growth Axis and Syndromes
- - Early life growth is important for pubertal growth and adult height
    
    ea0110p17
  - Genetic etiology of persistent short stature in chinese children born small for gestational Age
    
    ea0110p18
  - One year treatment with anastrozole increases predicted adult height in peri-pubertal boys with aggrecan deficiency
    
    ea0110p563
  - Macimorelin test: a safer and reliable alternative to the gold standard insulin tolerance test
    
    ea0110p564
  - Treatment with anastrozole alone or with GH increases final height in pubertal boys with short predicted adult height- real-world data
    
    ea0110p565
  - Effect of a short-term course of transdermal testosterone on growth, puberty and adult height in boys with constitutional delay of growth and puberty (CDGP)
    
    ea0110p566
  - Genetic insights into short stature: an evaluation of clinical, hormonal, and genetic parameters in a real world paediatric cohort
    
    ea0110p567
  - Evaluation of the pharmacokinetics (PK), pharmacodynamics (PD), and safety of the new capsule formulation of LUM-201, an oral growth hormone secretagogue
    
    ea0110p568
  - The need for early reassessment in children with growth hormone deficiency
    
    ea0110p569
  - Long-acting pegylated growth hormone in prepubertal children with turner syndrome: a 3-year multicenter study in China
    
    ea0110p570
  - Gastrointestinal and nutritional challenges in silver-russell syndrome: changes in management and outcomes since 2015
    
    ea0110p571
  - Does pubertal induction with transdermal or oral estrogen have an impact on uterine dimensions in Turner syndrome?
    
    ea0110p572
  - High diagnostic yield of WES in identifying monogenic causes of severe short stature in consanguineous children across three countries: importance of cellular mechanisms in extreme growth disorders
    
    ea0110p573
  - Evolving genetic influences on infant growth: a longitudinal analysis of polygenic scores and growth patterns in infancy
    
    ea0110p574
  - Effects of the ketogenic diet compared to the mediterranean diet in patients with acromegaly
    
    ea0110p575
  - Comparative efficacy of growth hormone, aromatase inhibitors, and gonadotropin-releasing hormone agonists in idiopathic short stature with advanced bone age
    
    ea0110p576
  - Long-acting PEGYlated recombinant human growth hormone (jintrolong) in short children born small for gestational age: 4-year results from a multicenter, randomized, dose-response trial in china
    
    ea0110p577
  - Aetiology of short stature in children originally diagnosed with idiopathic growth hormone deficiency: comprehensive genetic investigation of a single centre cohort
    
    ea0110p578
  - Comparison of oral vs intravenous glucose exposure on plasma growth hormone levels: a crossover study in healthy volunteers
    
    ea0110p579
  - Epidemiology of disorders associated with tall stature in childhood: a 20-year birth cohort study
    
    ea0110p580
  - Liver abnormalities in a population of adult women with turner syndrome
    
    ea0110p581
  - The growth paradox: unraveling the impact of advanced bone age on height potential in untreated conditions"
    
    ea0110p582
  - Efficacy of growth hormone therapy in children with npr2 and acan gene variants: a comparative study
    
    ea0110p583
  - Efficacy of somapacitan in treatment-fatigue adults with growth hormone deficiency previously treated with daily GH injections: a 24-week randomized active-controlled trial
    
    ea0110p584
  - Long-term maintenance in the upper normal IGF-1 levels has beneficial effects on body fat and marker of low-grade inflammation in adults with growth hormone deficiency
    
    ea0110p585
  - Analysis of functionally uncharacterized variants of the GH1 gene from patients with isolated growth hormone deficiency (IGHD)
    
    ea0110p586
  - Retrospective evaluation of the phenotypic-genotypic characteristics of patients with short stature who underwent next-generation sequencing analysis
    
    ea0110p587
  - The impact of dose modification guided by growth response monitoring on igf-1 levels and height velocity in growth hormone deficiency treatment
    
    ea0110p588
  - Real-world IGF-I variations & its management in children on recombinant human growth hormone (rhGH) therapy (RIGHT study)
    
    ea0110p589
  - Unexpected high frequency of copy number variations as genetic causes of failure to achieve catch-up growth in small for gestational age children: a multicenter study in Korea
    
    ea0110p590
  - Spinal deformities in patients with rasopathies and pathogenic variants in related genes
    
    ea0110p591
  - A genetic cause of tall stature is more often detected in children with familial tall stature compared to non-familial tall stature
    
    ea0110p592
  - Combined human growth hormone and gonadotropin-releasing hormone analog therapy improves pubertal growth in children with poor final height prognosis: a retrospective observational study
    
    ea0110p593
  - Development of muscle function in children with achondroplasia under vosoritide treatment
    
    ea0110p594
  - SEENEZ-trial: cost-analysis of withdrawing growth hormone treatment at mid-puberty in adolescents with transient idiopathic isolated growth hormone deficiency
    
    ea0110p595
  - Impact of methylphenidate on growth, thyroid function, and cortisol secretion in children with ADD/ADHD: a systematic review (2000-2024)
    
    ea0110p596
  - Long-term growth hormone therapy in a patient with hallermann-streiff syndrome: a 15-year follow-up
    
    ea0110p597
  - Short stature and growth hormone deficiency in a case of POMC deficiency: an unexpected clinical association
    
    ea0110p598
  - Impact of the TUITEK™ patient support program on caregivers-related behaviours in enhancing growth hormone treatment adherence
    
    ea0110p599
  - A novel point-of-care molecular diagnostic method for the rapid diagnosis of Turner syndrome
    
    ea0110p600
  - Genotype-phenotype correlations and clinical variability in noonan syndrome
    
    ea0110p601
  - Is the high incidence of false-positive results of growth hormone stimulation tests in children with short stature related to the nutritional status? Let's ask artificial intelligence
    
    ea0110p602
  - The medical impact of hypochondroplasia by age among adults in England between 1998 and 2019: a matched cohort study using electronic medical records from the clinical practice research datalink
    
    ea0110p603
  - Screening for shox gene variation in children with apparently idiopathic short stature: systematic screening or clinical and radiological oriented screening?
    
    ea0110p604
  - Long term follow-up in a patient with Cat Eye syndrome, hypopituitarism and hypertransaminasemia
    
    ea0110p605
  - Quality of life, sexuality, and psychosocial well-being in adult women with turner syndrome: insights from a danish questionnaire survey
    
    ea0110p606
  - Total and bioactive IGF-i in healthy children and adolescents and in short children during growth hormone therapy: an alternative tool to individualized GH treatment in patients
    
    ea0110p607
  - Frequency, detection and management of scoliosis in children with prader willi syndrome - experience of an irish tertiary referral centre
    
    ea0110p608
  - Characterization of bone health in an adult population with turner syndrome: insights from a monocentric cross-sectional study
    
    ea0110p609
  - Prevalence and growth pattern of poor long-term responders to gh therapy in prepubertal short children born small for gestational age: real life data from them belgian-luxembourgish registry BELGROW
    
    ea0110p610
  - Advancing precision in GH therapy: AI models for predicting IGF-1
    
    ea0110p611
  - EKAT-06 evidence based knowledge for monitoring childhood growth
    
    ea0110p612
  - Evaluation of growth velocity in patients with achondroplasia treated with vosoritide
    
    ea0110p613
  - Comparison of the effects of weekly and daily treatment on auxology, metabolism and quality of life in cases with growth hormone deficiency
    
    ea0110p614
  - Use of vosoritide in children with achondroplasia - clinical experience
    
    ea0110p615
  - Treatment in genetic short stature: growth hormone use in patients with npr2 heterozygous variants
    
    ea0110p616
  - The medical impact of hypochondroplasia among children in England between 1998 and 2019: a matched cohort study using electronic medical records from the clinical practice research datalink
    
    ea0110p617
  - Diagnosis of silver russell syndrome in 2025: is a scoring system still helpful?
    
    ea0110p618
  - GloBE-Reg: A global registry for evaluating the safety and effectiveness of growth hormone therapy across the age span
    
    ea0110p619
  - Clinical characteristics of children with mccune-albright syndrome in China: a retrospective cohort study
    
    ea0110p620
  - When genetics cast doubt on paternity
    
    ea0110p621
  - Impact of body mass index on growth hormone peak during insulin tolerance test in childrenand adolescents
    
    ea0110p622
  - Unraveling the genetic basis of short stature in pediatric patients: a whole exome sequencing approach
    
    ea0110p623
  - N-acetylcysteine treatment for skin-picking in children and young adults with pws: a randomized placebo-controlled cross-over trial
    
    ea0110p624
  - Challenges of puberty in turner syndrome: experience of a tertiary pediatric hospital
    
    ea0110p625
  - Quality of life improvements with GH, GnRHa, and AI therapies in children with short stature and advanced bone age
    
    ea0110p626
  - Effect of growth hormone therapy on final height in SHOX deficiency and turner syndrome: a single-center experience
    
    ea0110p627
  - Retrospective analysis of two databases on growth hormone treatment in chinese children with short stature - baseline characteristics and clinical inertia
    
    ea0110p628
  - Identifying relevant factors for recommendation of digital health solutions supporting paediatric growth hormone treatments in Finland: insights from participatory workshop
    
    ea0110p629
  - Continuous glucose monitoring (CGM) for assessing glycaemic variability in growth hormone deficient children shifting from recombinant GH daily injections to long-acting GH analogues: a case series
    
    ea0110p630
  - Comparison of leptin, ghrelin, and nesfatin levels in growth hormone deficiency and short stature patients before and after growth hormone therapy
    
    ea0110p631
  - Growth hormone therapy in noonan syndrome: impact on neurodevelopment and prognosis
    
    ea0110p632
  - Mysoconnect® for sogroya®: long-acting growth hormone for patients with growth-related disorders and their caregivers
    
    ea0110p633
  - Efficacy and safety of somapacitan vs daily growth hormone at 52 weeks in patients with growth hormone deficiency: pooled analysis of the randomised REAL 3, REAL 4 and REAL 6 clinical trials
    
    ea0110p634
  - Evaluation of features for a digital application for growth hormone therapy using perceptions gathered from patients, caregivers and healthcare professionals
    
    ea0110p635
  - Real-world data: effectiveness and safety of vosoritide in the treatment of achondroplasia in chinese population
    
    ea0110p636
  - Long-acting PEG-RHGH: insights from five-year outcomes in pediatric patients with growth hormone deficiency from CGLS database
    
    ea0110p637
  - Clinical delineation and genotype-phenotype correlation in 104 pediatric patients with kabuki syndrome: a large longitudinal cohort from a single center in china
    
    ea0110p638
  - Early growth hormone treatment enhances growth and nutritional status in silver-russell syndrome
    
    ea0110p639
  - The impact of growth retardation on quality of life
    
    ea0110p640
  - Assessing skeletal maturity in indian children: a comparative study of GP, GR, and TW3 methods
    
    ea0110p641
  - Factors influencing growth trajectory and adult height in children born small for gestational age and treated with growth hormone: a single center study
    
    ea0110p642
  - Childhood-onset growth hormone deficiency: transition from pediatric to adult endocrine care in the Netherlands
    
    ea0110p643
  - Effects of growth hormone (GH) and sex steroid therapy on brain structure and pituitary function in turner syndrome (TS)
    
    ea0110p644
  - Growth hormone therapy in children with congenital acyanotic heart disease and short stature: balancing growth and cardiac health
    
    ea0110p645
  - Should the initial dose of long-acting growth hormone therapy somatrogon for pediatric growth hormone deficiency be standard for each child?
    
    ea0110p646
  - Design of a phase 2, randomized, controlled, multicentre study of vosoritide treatment in children with idiopathic short stature
    
    ea0110p647
  - Phase 3 pivotal trial design of daily oral LUM-201's efficacy and safety in treatment-naive children with growth hormone deficiency (GHD) in randomized, double-blind, placebo-controlled study
    
    ea0110p648
  - Changes in body composition, ghrelin, adipokines, and FGF23 in growth hormone deficient children during rhGH therapy
    
    ea0110p649
  - Big data as a strategy in the development of population auxological studies
    
    ea0110p650
  - Non-evidence-based and off-label growth therapies - observations from consultations and practice patterns
    
    ea0110p651
- MTEabolism, Nutrition and Obesity
- - Dysregulation of RNA-Exosome machinery component EXOSC4 in MASLD-HCC progression
    
    ea0110p19
  - Setmelanotide in the Management of Pediatric Obesity Due to Genetic Disorders: Clinical Response and Quality of Life Assessment
    
    ea0110p20
  - Adverse waist-for-height ratio trajectories in childhood are associated with cardiometabolic and cardiovascular risk by age 10
    
    ea0110p652
  - Efficacy of treatment with combination dapagliflozin and metformin vs metformin alone in overweight and obese women with polycystic ovary syndrome: a randomized controlled trial
    
    ea0110p653
  - Enzymatic approach to neonatal hyperbilirubinemia
    
    ea0110p654
  - Growth trajectories of height and body composition in pre-pubertal and early pubertal stages across obesity transition groups: a longitudinal study
    
    ea0110p656
  - A comprohensive cohort analysis of 113 paediatric non-syndromic monogenic obesity
    
    ea0110p657
  - Assessing how the edmonton obesity staging system for pediatrics (EOSS-P) in childhood relates to mental health outcomes 7 years later: findings from the quality cohort
    
    ea0110p658
  - Benefits of ambulatory blood pressure monitoring over office blood pressure in children and adolescents with severe obesity: findings from the bern obesity in childhood and adolescence biorepository
    
    ea0110p660
  - Weight loss at 18 months of setmelanotide in 2-5-year-old patients with rare mc4r pathway diseases
    
    ea0110p661
  - Exosomal miRNA profile and its association with insulin resistance in obese children and NAFLD patients
    
    ea0110p662
  - Hepatic triglyceride export in acromegaly and the effects of treatment - a preliminary study
    
    ea0110p664
  - Phase II study to assess the efficacy and safety of pasireotide in patients with post-bariatric hypoglycaemia: PASIPHY study design
    
    ea0110p665
  - Empagliflozin: sex-specific effects on mitochondrial function and cellular redox-balance in HFPEF and MASLD
    
    ea0110p666
  - Diagnostic performance of triglyceride-glucose-based indices for identifying metabolic syndrome in paediatric populations
    
    ea0110p667
  - The rising burden of childhood obesity: prevention could start at primary school
    
    ea0110p668
  - The dutch experience with anti-obesity drugs in young adults and adults with prader-willi syndrome
    
    ea0110p669
  - Impact of a 4-week multidisciplinary prehabilitation program on tumor-related gene expression in patients with colon cancer: the ONCOFIT project
    
    ea0110p670
  - Comparison of insulin resistance indices in obese children and adolescents based on a 10-year data
    
    ea0110p671
  - Western diet-induced effects on renal glucose and sodium transporters - a novel mechanism in pathophysiology of the metabolic syndrome
    
    ea0110p672
  - Mesothelial cells act as critical mediator in hyperandrogenism-induced visceral obesity
    
    ea0110p674
  - Sex-specific effects of different dietary compositions and NO-synthase inhibition on mitochondrial respiration and cellular redox state in HFPEF and MASLD
    
    ea0110p675
  - Cardiometabolic profile between metabolically healthy obese (MHO) vs metabolically unhealthy obese (MUO) adolescents
    
    ea0110p676
  - Role of AMPK in preserving metabolic homeostasis in visceral adipose tissue and skeletal muscle in a PCOS rat model
    
    ea0110p677
  - Piezo1 activation suppresses bone marrow adipogenesis for healthy skeleton through inhibition of a mechanoinflammatory autocrine loop
    
    ea0110p678
  - The visceral adipose-derived hormone ANNEXIN A8 alleviates obesity-induced chronic inflammation via modulating macrophage functions
    
    ea0110p679
  - Recommendations for screening for polycystic ovarian syndrome (PCOS) in adolescents with obesity: are national and international management guidelines aligned?
    
    ea0110p680
  - Body fat percentage is associated with pubertal onset in boys and girls
    
    ea0110p681
  - Effect of oral glucose administration on ghrelin levels in normal heigh children born small for gestational age being in the first decade of their life
    
    ea0110p682
  - Cord blood exosomal miRNAS from small-for-gestational-age newborns associate with measures of subsequent catch-up growth and insulin resistance
    
    ea0110p683
  - Comparative analysis of GLP-1 receptor agonists, traditional glucose-lowering medications and traditional anti-obesity medications on skeletal outcomes in obese individuals with and without type 2 diabetes: a five-year propensity-score matched cohort study
    
    ea0110p684
  - Sex differences in white adipose tissue adaptation and insulin sensitivity in a diet-induced obesity mouse model
    
    ea0110p685
  - Characteristics of postmenopausal women with PCOS
    
    ea0110p686
  - Evolution and determinants of metabolic phenotypes from childhood into adulthood: data from the QUALITY cohort
    
    ea0110p687
  - Clinical, genetic characteristics and long-term follow-up of sitosterolemia in children
    
    ea0110p688
  - CASP3-mediated PARP1 cleavage promotes hepatocyte apoptosis in non-alcoholic fatty liver disease
    
    ea0110p690
  - Semaglutide as a promising treatment for hypothalamic obesity: a twelve-month case series on four females with craniopharyngioma
    
    ea0110p691
  - Long term effect of setmelanotide and semaglutide on a patient with severe obesity due to 16p11. 2 microdeletion, encompassing the SH2B1 gene
    
    ea0110p692
  - A case report of nevus excision under setmelanotide treatment
    
    ea0110p693
  - Early life determinants of body composition in healthy term-born children at age 5 years
    
    ea0110p694
  - Transient infantile hypertriglyceridemia: the first case from the state of qatar
    
    ea0110p695
  - Real-world outcomes of liraglutide treatment in children with obesity: beyond weight loss
    
    ea0110p696
  - Prevalence of obstructive sleep apnea syndrome in patients with lipodystrophy: a retrospective analysis
    
    ea0110p697
  - The effect of GLP-1 administration on food intake in people with weight regain post-metabolic surgery
    
    ea0110p699
  - Development of a gas chromatography mass spectrometry method for urinary oestrogen profiling in pre- and postmenopausal women
    
    ea0110p700
  - Cumulative effects of genetic variants detected in a patient with early-onset non-syndromic childhood obesity
    
    ea0110p701
  - Metabolomic mechanisms involved in the impact of liver injury on elevated coronary heart disease risk
    
    ea0110p702
  - Multi-omics characteristics of balanced diet combined with high-intensity interval training for weight loss in obese children
    
    ea0110p703
  - Mental health in 10 year old children with overweight
    
    ea0110p704
  - Role of ligand- and genetic variant dependent melanocortin 4 receptor (MC4R) bias signaling for the individual risk to develop obesity
    
    ea0110p705
  - Sex Hormone-binding globulin prevent carbon tetrachloride-induced liver fibrosis development
    
    ea0110p706
  - The beta-2-adrenoreceptor agonist fenoterol increases resting enery expenditure without activation of brown adipose tissue in humans
    
    ea0110p707
  - Sex hormones and high-fat, high-sucrose diets: unraveling their interaction on brown adipose tissue morphology and gene expression
    
    ea0110p708
  - Anthropometric and metabolic assessment in adults with down syndrome: the need for novel indices and customized criteria
    
    ea0110p709
  - Frequency of monogenic variants in a cohort of individuals with severe, early-onset obesity from a single large tertiary paediatric centre
    
    ea0110p710
  - Clinical significance of urine NAG and blood Cys-C in early renal damage assessment of children with simple obesity
    
    ea0110p711
  - Association between 25-hydroxyvitamin-D and insulin resistance in korean adolescents: findings from the 2008-2014 KNHANES
    
    ea0110p712
  - Investigate the role of insulin in regulating the local expression of aromatase in the growth plate
    
    ea0110p713
  - Muscle respiratory capacity correlates with insulin sensitivity independent of adiposity and metabolic flexibility
    
    ea0110p714
  - Educational cartoon in the podiacar PROject: an approach to combat paediatric obesity
    
    ea0110p715
  - Combination therapy of semaglutide and methylphenidate leads to significant weight loss in prader-willi syndrome patients
    
    ea0110p716
  - Body mass index trajectories from early childhood to late adolescence: an analysis of the leicester respiratory cohorts
    
    ea0110p717
  - Effectiveness of simulation-based learning in enhancing confidence and clinical competence in managing lipid-related diseases: a mixed-methods study
    
    ea0110p718
  - AIP deficiency in zebrafish causes loss of intestinal epithelial differentiation via disrupted wnt signaling
    
    ea0110p719
  - Development of a novel thyroid hormone profiling method using liquid chromatography tandem mass spectrometry
    
    ea0110p720
  - Relation of a-synuclein level to glucotoxicity, lipotoxicity and cerebral neurodegeneration in children with obesity
    
    ea0110p721
  - Beneficial effects of oleocanthal-rich olive oil on platelet functionality and other metabolic parameters of type II diabetic patients
    
    ea0110p722
  - Oxyntomodulin as a biomarker for metabolic dysregulation and obesity: pathophysiological insights and screening potential
    
    ea0110p723
  - Weighing the benefits: maternal and fetal health post-bariatric surgery
    
    ea0110p724
  - Rhein induces adipose browning via inhibition of glucocorticoid receptor
    
    ea0110p725
  - Effects of maternal pre-pregnancy body mass index and gestational weight gain on body composition and blood sugar in three-year-old offspring
    
    ea0110p726
  - Serum and liver lipidome following empagliflozin administration for six months in a fast food diet mouse model
    
    ea0110p727
  - Single point insulin sensitivity estimator (SPISE) for cardiovascular risk assessment in pediatric central nervous system cancer survivors (PCNSCSs): a practical approach for early detection
    
    ea0110p728
  - Real-world results of genetic testing and performance of clinical criteria for familial hypercholesterolemia in a targeted young adult population
    
    ea0110p729
  - Distinct response of the human plasma lipidome to cold and fenoterol
    
    ea0110p730
  - Evaluation of the relationship between IGF-1 and systemic immune-inflammatory markers and metabolic comorbidities in patients with obesity
    
    ea0110p731
  - The french prader-willi registry: an essential tool for clinic and research on prader-willi syndrome
    
    ea0110p732
  - A case of familial monogenic obesity: the role of MC4R mutation in childhood obesity
    
    ea0110p733
  - Association of childhood BMI with height growth pattern and adult stature: mendelian randomization study
    
    ea0110p734
  - Non-high-density lipoprotein cholesterol for screening dyslipidemia in overweight Korean children
    
    ea0110p735
  - Mediating role of prepubertal adiposity in the association between breastfeeding and central precocious puberty: a nationwide cohort study
    
    ea0110p736
  - Pairing obesity medication with health behaviour and lifestyle therapy: a single center experience
    
    ea0110p737
  - Perceived self-efficacy in the management of childhood overweight and obesity: a study of hungarian paediatricians
    
    ea0110p738
  - Muscle ultrasound (US) characterization in patients with lipodystrophy and potential metabolic correlates
    
    ea0110p739
  - Association between body composition, lipid profile, inflammatory markers and fatty acid composition in healthy women: a cross-sectional study
    
    ea0110p740
  - Transforming lives: the impact of liver transplantation in treating glycogen storage disease type 1a - a case report
    
    ea0110p741
  - Macrophage glucocorticoid and androgen metabolism influence muscle cell metabolism
    
    ea0110p742
  - The effect of stress resiliency level and maternal diet on the metabolic health of offspring
    
    ea0110p743
  - Evaluating lipid ratios for cardiometabolic risk and insulin resistance in obese children
    
    ea0110p744
  - Relationship between body mass index and 1 mg dexamethasone suppression test in obese patients
    
    ea0110p745
  - Obesity effect on epicardial fat thickness in children
    
    ea0110p746
  - Limited preventive effects of empagliflozin against metabolic dysfunction-associated steatotic liver disease in a mouse model of fast food diet
    
    ea0110p747
  - Visceral adipose tissue as an important predictor of TBS
    
    ea0110p748
  - Nutritional habits and weight perception in childhood cancer survivors: insights for long-term health
    
    ea0110p750
  - Body composition phenotyping and BIA-DXA agreement for fat mass assessment in pediatric obesity: an exploratory study
    
    ea0110p751
  - Metabolic-associated steatotic liver disease and arterial stiffness in obese children: early cardiometabolic insights - a preliminary study
    
    ea0110p752
  - SPISE index: a novel predictor for identifying metabolically healthy obesity and cardiovascular risk in obese children
    
    ea0110p753
  - Successful treatment of two children with POMC deficiency using setmelanotide: a one-year review
    
    ea0110p754
  - Circulating levels of ghrelin in patients with a rare neurodevelopmental disorder associated with hyperphagia, and/or overweight, and/or obesity - the hogrid study
    
    ea0110p755
  - Prevalence of obesity in swiss children's hospitals: first results from the swisspedgrowth project
    
    ea0110p756
  - Metabolic profile of paediatric patients with silver-russell syndrome (SRS) or temple syndrome (TS)
    
    ea0110p757
  - Genetic causes and clinical features identified through a genetic diagnostic programme in cases of early-onset severe obesity
    
    ea0110p758
  - Early use of setmelanotide in severe hypothalamic obesity leads to weight stabilization with a significant improvement in the quality of life
    
    ea0110p759
  - Metabolic associated fatty liver disease (MAFLD) in patients with cushing syndrome
    
    ea0110p760
  - The influence of body mass index and physical activity on menarche: a comparative study between regular and boarding school students
    
    ea0110p761
  - Evaluation of pulse wave velocity as early indicator of vascular damage in children and adolescents with heterozygous familial hypercholesterolemia
    
    ea0110p762
  - The association of ciruculating spexin, obesity, and metabolic parameters in Korean children and adolescents
    
    ea0110p763
  - ?ral administration of Crocus sativus tepals extract improves systemic glucose tolerance in mice fed a high-fat diet through changes in gut microbiota composition
    
    ea0110p764
  - Higher BMI as a protective factor for the development of ketotic hypoglycaemia in children with vomiting and dehydration
    
    ea0110p765
  - Tryptophan derivatives as non-invasive diagnostic indicators for obesity-related MASLD in children and adolescents
    
    ea0110p766
  - Postprandial metabolic response to intake of different milk fat structures in healthy individuals
    
    ea0110p767
  - Ketone supplementation acutely lowers androgen and glucose levels in women with polycystic ovary syndrome (PCOS)
    
    ea0110p768
  - When hunger defies satiety: insights from a case of LEPR-related monogenic obesity
    
    ea0110p769
  - Comparison of ambulatory glucose profile (AGP) parameters between two advanced hybrid closed-loop (AHCL) systems from childhood to adulthood at 6 and 12 months
    
    ea0110p770
  - VLCKD improves MASLD and metabolic dysfunction in patients with type 2 diabetes and obesity
    
    ea0110p771
  - Serum inflammation based scores in prediction of liver fibrosis among cushing syndrome and MACS patients: data from ERCUSYN krakow database
    
    ea0110p772
  - Endocrine manifestations in pediatric patients with inherited metabolic diseases
    
    ea0110p773
  - Metabolic profile of patients with albuminuria and previously undiagnosed chronic kidney disease according to the AURA register
    
    ea0110p774
  - Analysis of the concordance between body fat percentage estimated by dual-energy X-ray absorptiometry (DEXA) and anthropometric parameters in a cohort of obese patients
    
    ea0110p775
  - Setmelanotide treatment in genetic obesity: a single-center experience
    
    ea0110p776
  - The impact of prader-willi syndrome (PWS) on caregivers and the healthcare system: a burden of illness study design
    
    ea0110p777
  - Linking metabolic syndrome and physical fitness in children with obesity: a cross-sectional study from the PODiaCar project
    
    ea0110p778
  - Management and diagnosis of moderate and severe hypernatraemia in a UK district hospital: a retrospective audit
    
    ea0110p779
  - Patient and caregiver experiences with setmelanotide treatment in bardet-biedl syndrome - real-world evidence and a patient support program
    
    ea0110p780
  - Real life data of obesity in craneopharyngiomas in an pediatric/adult transition pituitary unit
    
    ea0110p781
- Multisystem Endocrine Disorders
- - Genome Edited Human Cell Lines For Studying Steroidogenesis In P450 Oxidoreductase Deficiency
    
    ea0110p21
  - -Week Results from the HELIOS Trial: A Phase 2, Open-Label Study Evaluating an Oral, Fixed-Dose Combination of Sodium Phenylbutyrate and Taurursodiol in Wolfram Syndrome
    
    ea0110p22
  - Post-authorisation safety study of ketoconazole HRA in endogenous cushing's syndrome: seventh annual interim report in 108 patients
    
    ea0110p782
  - Genetic and clinical insights into triple a syndrome in a multi-ethnic population: a large cohort from sudan
    
    ea0110p783
  - Factors affecting the prevelance of endocrinopathies in transfusion dependent thalassemia patients in the national thalassemia centre, kurunegala, sri lanka
    
    ea0110p784
  - Endocrine disorders in patients with neurofibromatosis type 1: a single-center prevalence study
    
    ea0110p785
  - Autoimmune diseases in 3, 812 danish transgender persons and 38, 120 cisgender controls before and after transgender care. a register based cohort study
    
    ea0110p786
  - Muscle characteristics in adult patients with APECED
    
    ea0110p787
  - EMPOWER-TRANS* - development and implementation of innovative, digital information and training concepts for children with gender incongruence/gender dysphoria (GI/GD) and their families
    
    ea0110p788
  - Clinical presentation and genotype-phenotype association of 95 patients with pathogenic mutation in the menin gene
    
    ea0110p789
  - Is hypernatremia related to insulin resistance in type 1 myotonic dystrophy?
    
    ea0110p790
  - Systematic analysis and network mapping of disease associations in autoimmune polyglandular syndrome
    
    ea0110p791
  - Endocrine involvement in a wide cohort of children and adults affected by 22q11.2 Deletion Syndrome
    
    ea0110p792
  - Associations of healthy lifestyle with all-cause and cardiovascular disease mortality in patients with cardiovascular-kidney-metabolic syndrome: two prospective cohort
    
    ea0110p793
  - First comprehensive quantification of the human endocrinome: patterns in hormone distribution and their physiological significance
    
    ea0110p794
  - Respiratory and sleep disorders in children with prader willi syndrome: prevalence and characterization
    
    ea0110p795
  - Evaluation of the relationship between metabolic-associated fatty liver disease and sarcopenic obesity in patients with diabetes
    
    ea0110p796
  - Abstract unavailable
    
    ea0110p797
  - Decoding clinical heterogeneity in ornithine transcarbamylase deficiency: novel mutations and therapeutic outcomes from a longitudinal cohort study
    
    ea0110p798
  - Successful transition strategies in turner syndrome
    
    ea0110p799
  - Algorithmic approach for the of hashimoto's thyroiditis: a case control indian study
    
    ea0110p800
  - Efficacy and safety of finerenone in type 2 diabetes with chronic kidney disease
    
    ea0110p801
  - Clinical characteristics and influencing factors of children with MT-TL1 gene m.3243A>G mutation: a phenotypic study based on 11 han chinese patients
    
    ea0110p802
  - The role of MRI and ferritin in assessing iron overload and endocrine dysfunction in thalassemia major: focus on pituitary MRI findings
    
    ea0110p803
  - Assessment of facial morphologic features in patients with polycystic ovary syndrome using deep learning:a multi-center cross-sectional study
    
    ea0110p804
  - Telomere length in patients with type 2 diabetes: impact of chronic kidney disease
    
    ea0110p805
  - Prevalence, incidence and risk factors for dysnatremia in european community-dwelling older adults - a secondary analysis of the DO-HEALTH trial
    
    ea0110p806
  - Endocrinopathies in turkish children with inborn errors of immunity: a single-center experience
    
    ea0110p807
  - A case of atypical wolfram syndrome with late diagnosis and without diabetes inspidus component
    
    ea0110p808
  - Coexistence of thyroid autoimmunity with adrenal disease: clinical implications and insights
    
    ea0110p809
  - Chronic hypoparathyroidism video-based CME series improved physician knowledge to prepare for an era of emerging therapies
    
    ea0110p810
  - Case-based rare disease CME significantly improves competence in diagnosing mct8 deficiency in pediatric/endocrinology practice
    
    ea0110p811
  - Multiple endocrine neoplasia type 4 (MEN4) syndrome due to rare pathogenic variant of CDK1B gene: a case report
    
    ea0110p812
  - Coexistence of papillary and medullary thyroid carcinomas in a patient with MEN2A
    
    ea0110p813
  - A case report of mccune-albright syndrome with hepatic focal nodular hyperplasia and review of literature
    
    ea0110p814
  - Quality of XLH care in the nordics: perspectives of parents with children with XLH
    
    ea0110p815
  - Association between body mass index (BMI) and immune-related adverse events among cancer patients receiving immune checkpoint inhibitors: a single institution analysis
    
    ea0110p816
  - Different faces of polycystic ovary syndrome: contrasting clinical and biochemical profiles in adolescents and adults
    
    ea0110p817
  - The role of pituitary MRI in assessing endocrine dysfunction and growth defects in thalassemia major
    
    ea0110p818
  - Comparative analysis of MRI and ferriscan in thalassemia major and intermedia: implications for growth, puberty, and endocrine health"
    
    ea0110p819
  - An intricate case of postmenopausal hyperandrogenism: causes and consequences
    
    ea0110p820
  - Endocrine monitoring when initiating immunotherapy in cancer patients: a quality improvement project
    
    ea0110p821
  - Large pheochromocytoma and primary hyperparathyroidism associated with a rare mutation in the succinate dehydrogenase a (SDHA) gene
    
    ea0110p822
- Pituitary, Neuroendocrinology and Puberty
- - Genetic basis of patients with congenital gonadotropin deficiency
    
    ea0110p23
  - The roles of PDLIM1 in silent corticotroph adenomas aggressiveness
    
    ea0110p24
  - Severe hyponatraemia in Europe: insights into endocrinologists' clinical practices and perspectives
    
    ea0110p25
  - Piperonyl butoxide: a putative novel endocrine disruptor causing Cushing Syndrome
    
    ea0110p823
  - The personality profile and neurostructural associations in patients with cushing's disease
    
    ea0110p824
  - Using genomics to characterize features of aggressiveness in PitNETs
    
    ea0110p825
  - Short-term efficacy of Stanozolol or recombinant human Growth hormone in CPP or EFP boys with excessive growth deceleration during GnRHa treatment
    
    ea0110p826
  - Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variants
    
    ea0110p827
  - [18F]Fluorethyltyrosine positron emission tomography for localisation of corticotroph pituitary adenomas in the initial evaluation of Cushing's disease
    
    ea0110p828
  - Overphosphorylation of the LKB1 signalling pathway proteins in sparsely granulated somatotropinomas
    
    ea0110p829
  - The endowatch - developing an 'external hypothalamus' to support patients (and their parents) with hypothalamic dysfunction
    
    ea0110p830
  - Survival in patients with pituitary carcinoma
    
    ea0110p831
  - A mouse luteinizing hormone-blocking monoclonal antibody; development and in vivo proof of blocking capacity
    
    ea0110p832
  - Understanding the developmental down-regulation of mkrn3 at puberty through bioinformatics and experimental approaches
    
    ea0110p833
  - sz-arrestin 2 protein expression correlated with non-functioning pituitary neuroendocrine tumors (NF-PitNETs) in vitro responsiveness to dopamine agonists
    
    ea0110p834
  - Validation of the PANOMEN-3 predictive model for tumor recurrence and progression in pituitary tumors. a real-world spanish multicenter study
    
    ea0110p835
  - Urea-stimulated copeptin: a novel diagnostic approach in polyuria polydipsia syndrome
    
    ea0110p836
  - Prognostic study of suspected dual CHH patients treated with gonadotropins
    
    ea0110p837
  - Omentin-1 as a new regulator of porcine pituitary function: in vitro effect on global proteome, endocrinology, and signaling pathways
    
    ea0110p838
  - Insulin-like growth factor 1 as a diagnostic marker to differentiate progressive central precocious puberty from non-progressive precocious puberty: a prospective study
    
    ea0110p839
  - It is quite stressful to be a stem cell
    
    ea0110p840
  - Development and validation of rapidly progressive central precocious puberty diagnostic prediction models in girls
    
    ea0110p841
  - Impact of pasireotide LAR on lipid and glucose metabolism in patients with acromegaly: a systematic review and meta-analysis
    
    ea0110p842
  - The role of functional imaging with 11C-methionine and 11F-tyrosine in patients with cushing's disease
    
    ea0110p843
  - Natural history of non-functioning pituitary microadenomas in clinically diagnosed MEN 1 syndrome
    
    ea0110p844
  - High risk of psychiatric morbidity in patients with acromegaly: a cohort study and meta-analysis
    
    ea0110p845
  - Involvement of menin, p27 and pakt in prolactinoma development. sexual differences
    
    ea0110p846
  - Multicentre 30-year data on the 4-mg intravenous dexamethasone suppression test in the diagnosis of cushing's syndrome
    
    ea0110p847
  - Laterality of amygdalavolume of brain in different genders help predict individuals with ambiguous genitalia of disorders of sexual development
    
    ea0110p848
  - Musculoskeletal disorders in acromegaly: a national, registry-based cohort study
    
    ea0110p849
  - Thromboprophylaxis of venous thromboembolism in endogenous cushing's syndrome: recommendations from a delphi panel consensus position statement
    
    ea0110p850
  - Safety and effectiveness of >8 years of osilodrostat treatment in patients with cushing's disease: findings from the LINC rollover open-label, multicentre study
    
    ea0110p851
  - Testosterone vs gonadotropin therapy for induction of puberty in boys with congenital hypogonadotropic hypogonadism
    
    ea0110p852
  - Delayed puberty and intellectual disability: in a boy with a 15q11.2-q13. interstitial duplication including MKRN3 gene
    
    ea0110p853
  - Genetic characterization of pituitary neuroendocrine tumours in the maltese population
    
    ea0110p854
  - Pasireotide induces long-term cystic degeneration of somatotrophic pituitary neuroendocrine tumors (PitNETs)
    
    ea0110p855
  - Acromegaly management beyond primary surgery: efficacy and safety of repeat surgery and radiotherapy
    
    ea0110p856
  - Impact of compressive neuropathy on peripapillary retinal nerve fiber layer thickness in pediatric patients after craniopharyngioma surgery
    
    ea0110p857
  - Prognostic factors of the level of cognitive functioning in children after craniopharyngioma treatment
    
    ea0110p858
  - The natural course of macroincidentalomas: a retrospective study of a single reference center
    
    ea0110p859
  - Immunohistochemical biomarkers in acromegaly: predicting treatment response and associations with tumor characteristics
    
    ea0110p860
  - Neurophysin I: a reliable, novel, and robust biomarker for oxytocin an analysis of a double-blind placebo-controlled cross-over trial
    
    ea0110p861
  - Clinical presentation and outcomes of pituitary apoplexy in patients with PitNETs: an Italian multicentric study
    
    ea0110p863
  - Generation and interrogation of a consensus multi-omics atlas for pituitary gland research
    
    ea0110p865
  - Preliminary results from the core registry-gender incongruence module: current insights and future directions
    
    ea0110p866
  - Worldwide secular changes in limits for age at thelarche: an updated systematic review and meta-analysis
    
    ea0110p867
  - The role of caSR for gonadotropin release in male mice
    
    ea0110p868
  - Calcium directly influences pituitary function in female mice through the calcium sensing receptor (CaSR)
    
    ea0110p869
  - Osilodrostat prior and new use in patients with endogenous cushing's syndrome: 2-year interim analysis results (safety and effectiveness) from the real-world non-interventional LINC 6 study
    
    ea0110p870
  - Hypogonadotropic hypogonadism diagnosis in boys under one year of age based on gonadotrophins, testosterone, antimullerian hormone (AMH) and inhibin B (INHB) measurements
    
    ea0110p871
  - Long-term outcome after craniopharyngioma in childhood: the role of treatment in specialized centers
    
    ea0110p872
  - Outcome of hypercortisolism screening tests and morning plasma ACTH in the differential diagnosis of ACTH-dependent cushing's syndrome: results from a large European multicenter study
    
    ea0110p873
  - Immune-related hypophysitis and imaging: a distinct type of hypophysitis?
    
    ea0110p874
  - Progression of potentially aggressive PitNETs after radiotherapy: risk factors, management, and outcomes
    
    ea0110p875
  - Clinical exome sequencing study of growth hormone secreting pituitary tumors
    
    ea0110p876
  - "Liver fibrosis and steatosis markers- FIB-4 and HSI in acromegaly: a single-center observational study"
    
    ea0110p877
  - The clinical course and the systemic inflammation biomarkers (SIBs) differ between giant and not-giant aggressive prolactinomas
    
    ea0110p878
  - Acromegaly detection from facial images using machine learning
    
    ea0110p879
  - Hyponatremia correction is associated with increased brain-derived neurotrophic factor levels (BDNF) - subanalysis of a randomized, double-blind, placebo-controlled, crossover trial
    
    ea0110p880
  - Perception and psychological effects of central precocious puberty or early normal puberty, and its treatment among girls and their caregivers
    
    ea0110p881
  - Hemodynamic changes in patients with idiopathic central precocious puberty treated with gonadotropin-releasing hormone (GnRH) analogue
    
    ea0110p882
  - "Endocrine and genetic influences on neurodevelopment: insights from neuroimaging in turner syndrome"
    
    ea0110p883
  - Spliceosome approach for the identification of diagnostic and prognostic biomarkers and therapeutic targets in paediatric brain tumors
    
    ea0110p884
  - Refining pituitary adenoma classification: the role of transcription factors in diagnosis and risk assessment
    
    ea0110p885
  - Persistent HPG axis reactivation: a conundrum in transgender male adolescents on gender-affirming testosterone therapy
    
    ea0110p886
  - Expression of asprosin, furin and Olfr734 in the pituitary during the estrous cycle in control and obese mice. in vitro effect of asprosin on pituitary cell proliferation
    
    ea0110p887
  - Impact of disease activity on cognitive and psychological outcomes in acromegaly: a prospective study
    
    ea0110p888
  - Primary empty sella and pituitary insufficiency - a retrospective analysis
    
    ea0110p889
  - Long-term safety of pasireotide in patients with acromegaly: final results from a 10-year open-label phase iv rollover study (B2412)
    
    ea0110p890
  - Endoscopic ultrasound-guided radiofrequency ablation is a safe and efficient treatment of symptomatic insulinomas - a single center experience of 14 patients
    
    ea0110p891
  - Changes in prevalence and incidence of pituitary neuroendocrine tumours: a 25-year population based study in malta
    
    ea0110p892
  - Folliculo-stellate cells in a series of ACTH-secreting pituitary neuroendocrine tumors
    
    ea0110p893
  - Clinical, metabolic, bone and body composition characteristics of patients with various causes of childhood growth hormone deficiency (COGHD) in the transition period - a single center study
    
    ea0110p894
  - The effect of MDMA on the anterior pituitary
    
    ea0110p895
  - Exenatide for diagnosing endogenous hyperinsulinemic hypoglycaemia - a randomised placebo-controlled, double-blind, cross-over proof-of-principle study - fast study
    
    ea0110p896
  - Changes in circulating levels of miR-30b during minipuberty and puberty in girls
    
    ea0110p897
  - Depression, cognitive dysfunction and anxiety in illicit androgenic steroid users' years after cessation of usage
    
    ea0110p898
  - Hypothalamic-pituitary abnormalities in paediatric histiocytosis: preliminary retrospective data from a large cohort of a tertiary italian center
    
    ea0110p899
  - Aggressive pituitary adenomas and pituitary carcinomas
    
    ea0110p900
  - Validation of arginine-stimulated copeptin cut-offs for diagnosing AVP deficiency (central diabetes insipidus)
    
    ea0110p901
  - Central diabetes insipidus and panhypopituitarism in acute myeloid leukemia
    
    ea0110p902
  - GLP-1 agonist semaglutide for the treatment of acquired hypothalamic obesity in adolescents: efficacy, adverse effects and impact on quality of life and eating behaviours
    
    ea0110p903
  - Repurposing dasatinib, an FDA-approved tyrosine kinase inhibitor, for the treatment of aggressive pituitary tumors
    
    ea0110p904
  - Macroorchidism and elevated inhibin B levels as key indicators of an extremely rare manifestation of mccune-albright syndrome in boys
    
    ea0110p905
  - Toward earlier diagnosis of childhood suprasellar brain tumors through improved growth monitoring
    
    ea0110p906
  - The association between gonadotropin-releasing hormone analogue use and body mass index in girls with idiopathic central precocious puberty or early puberty: a systematic review and meta-analysis
    
    ea0110p907
  - Age-related differences in the clinical features and management of pituitary apoplexy: insights from a spanish cohort study
    
    ea0110p908
  - Body mass index does not influence the gh response in the oral glucose tolerance test for the diagnosis of acromegaly
    
    ea0110p909
  - Sleep quality, depression and anxiety in patients with hypopituitarism - an international survey study
    
    ea0110p910
  - Evaluation of internalizing symptoms in mothers of girls diagnosed with central precocious puberty: a pre- and post-treatment analysis
    
    ea0110p911
  - A case of aggressive AIP-mutated pituitary acrogigantism treated with pasireotide
    
    ea0110p912
  - Cytokines and chemokines modulate the growth of pituitary adenoma/neuroendocrine tumors: preliminary results of a monocenter prospective pilot study
    
    ea0110p913
  - Aggressive prolactinomas: unveiling mechanisms of dopamine agonist resistance through exomic, tanscriptomic, and metabolic strategies
    
    ea0110p914
  - "Cortisone-loop" an educational tool that ensures the quality of care for children with adrenal insufficiency in sweden, how does it work in practice? evaluation in nirthern sweden
    
    ea0110p915a
  - Biological maturity and body composition changes during pubertal growth: a longitudinal study of korean adolescents
    
    ea0110p916
  - Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective
    
    ea0110p917
  - Update on the use of robotic surgery and artificial intelligence for pituitary tumors
    
    ea0110p918
  - Defective Nitric oxide pathway signalling - a link between premature birth and altered mini-puberty?
    
    ea0110p919
  - A phase 2, open-label, multiple-ascending-dose trial evaluating anti-ACTH antibody lu AG13909 in adults with cushing's disease: balanced trial design
    
    ea0110p920
  - MRI-based radiomics of the pineal gland in girls does not provide informative data for the diagnosis of central precocious puberty
    
    ea0110p921
  - Hormonal support for very young transgender adolescents aligns body composition with identified gender
    
    ea0110p922
  - Shredded AIP pituitary sequel
    
    ea0110p923
  - The prevalence of brain abnormalities in children with central precocious puberty or early and fast puberty
    
    ea0110p924
  - Glucocorticoid withdrawal syndrome, a potential marker for prolonged remission after transsphenoidal surgery in cushing's disease: insights from a single center 20-year retrospective cohort
    
    ea0110p925
  - "Bioimpedance vector analysis in hyponatremic patients with syndrome of inappropriate antidiuresis: a prospective multicenter study"
    
    ea0110p926
  - Macular ganglion cell complex thickness and the post-illumination pupil response before and after chiasm decompression in pituitary adenoma patients with and without visual field loss
    
    ea0110p927
  - Complete remission of headaches in aggressive pitnets treated with pasireotide. correlation with systemic inflammation biomarkers (SIBs)
    
    ea0110p928
  - Hyponatremia in severe hypothyroidism ("the HYPO2 study")
    
    ea0110p929
  - Effects of dulaglutide on oxytocin plasma levels in healthy men: a secondary analysis of a randomized, double-blind, placebo-controlled crossover study
    
    ea0110p930
  - Disrupted ACTH and cortisol response to osmotic and non-osmotic stress in patients with AVP-deficiency
    
    ea0110p931
  - Long-term outcomes of gonadotropin-releasing hormone analogue-treated obese girls with central precocious puberty
    
    ea0110p932
  - Early prolactin normalization and tumor shrinkage predict the first-year response to cabergoline treatment in invasive macro-giant prolactinomas
    
    ea0110p933
  - Early life exposure to antibiotics and precocious puberty in children: a nationwide population-based cohort study
    
    ea0110p934
  - Exosomal miRNA expression profiles and pathway enrichment analysis in girls with central precocious puberty and premature thelarche
    
    ea0110p935
  - Optimizing laboratory defined macroprolactin algorithm for follow-up patients
    
    ea0110p936
  - Discrepancy between central and peripheral ACTH response to desmopressin stimulation: two cases
    
    ea0110p937
  - Medium-term effects of surgical therapy vs. medical treatment in patients with remission of cushing's disease
    
    ea0110p938
  - Effect of bone age at GnRH agonist treatment cessation on near adult height in korean girls with central precocious puberty
    
    ea0110p939
  - Neurofibromatosis type 1 in the eyes of an endocrinologist - a disease requiring a coordinated care
    
    ea0110p940
  - Galactorrhea and headache in an 18-year-old transfeminine youth: a case report
    
    ea0110p941
  - Temperament, character, and quality of life in patients with acromegaly: factors affecting psychosocial processes
    
    ea0110p942
  - Septo-optic dysplasia: clinical phenotype and impact on the child and family
    
    ea0110p943
  - Impact of gender-affirming hormone therapy on cardiovascular function: a cross-sectional study
    
    ea0110p944
  - CAm²029 octreotide subcutaneous depot provides stable control of IGF-I and improves key symptoms throughout a 4-week post-dose interval: analysis from the ACROINNOVA 1 trial
    
    ea0110p945
  - BMI trajectories during childhood in girls with precocious puberty: a national register-based study
    
    ea0110p947
  - The intra-individual periodicity of serum GH patterns in acromegaly is very high and independent of disease control: analysis of 650 GH time series from 106 patients
    
    ea0110p948
  - Cardiovascular morbidity in acromegaly
    
    ea0110p949
  - Soluble alpha Klotho concentrations in patients with pituitary adenomas
    
    ea0110p950
  - Endocrine challenges in hypothalamic-pituitary region tumors in pediatric population: a greek children's hospital perspective
    
    ea0110p951
  - A case of severe ACTH-dependent cushing syndrome
    
    ea0110p952
  - Diagnostic delay in children with intracranial germ cell tumour and high burden of endocrinopathies among survivors
    
    ea0110p953
  - DISCERN: delta copeptin in the investigation of SIAD and CSW: evaluating the role of a novel biomarker
    
    ea0110p954
  - CAM2029, a self-administered subcutaneous octreotide depot, improved pros and symptoms in patients with ACROMEGALY in the acroinnova 2 phase 3 trial: final analysis of the core phase results
    
    ea0110p955
  - Metformin administration improves treatment response in non-diabetic patients with acromegaly
    
    ea0110p956
  - Medical treatment in acromegaly: imunohistochemical features of responder patients
    
    ea0110p957
  - Defining the clinical value of MYD88, a component of the inflammasome machinery, as a diagnosis, prognosis and therapeutic tool in brain endocrine cancers
    
    ea0110p958
  - Menstrual health: schoolgirls' knowledge and hygiene practices
    
    ea0110p959
  - From CRH to the desmopressin era: a comparative study of stimulation tests in cushing's disease
    
    ea0110p960
  - The effect of GNRHA therapy initiation age on final height in girls with central precocious puberty
    
    ea0110p961
  - A rare cause of isolated hypogonadotrophic hypogonadism: spry4 gene mutation
    
    ea0110p962
  - A scoping review to explore eating behaviour and psychological mechanisms associated with obesity in patients with craniopharyngioma
    
    ea0110p963
  - An assesment of data completeness in GloBE-Reg, an international registry for studying saftey & effectiveness of novel therapies
    
    ea0110p964
  - Case series and review of the literature on the surgical management of hypophysitis: the endocrine outcome seems to be worsened by surgery
    
    ea0110p965
  - "Long-term hormonal and clinical outcomes in empty sella syndrome: a retrospective cohort analysis"
    
    ea0110p966
  - Clinical manifestations and health care utilisation in septo-optic dysplasia, with particular focus on overweight and obesity
    
    ea0110p967
  - Clinicopathological characteristics associated with the prognosis of recurrent gonadotroph tumors
    
    ea0110p968
  - Glucagon stimulation test and insulin tolerance test provide equally strong stimulus for growth hormone and cortisol secretion: a cross-over study
    
    ea0110p969
  - Sellar and parasellar lesions in the childhood, adolescence and transition age
    
    ea0110p970
  - A Novel autosomal recessive multiple pituitary hormone deficiency and obesity syndrome associated with the SH2B1 gene
    
    ea0110p971
  - Delayed puberty as the initial presentation of combined oxidative phosphorylation deficiency 55
    
    ea0110p972
  - Long-term safety and efficacy of once-daily oral paltusotine in the treatment of patients with acromegaly: ACROBAT advance year 4 analysis
    
    ea0110p973
  - Natural history of non-functioning pituitary microadenomas: A systematic review and individual participant data meta-analysis
    
    ea0110p974
  - Giant cell tumour of the bone mimicking pituitary macroadenoma: a case report
    
    ea0110p975
  - The systemic effects of hormone replacement therapy for central hypoadrenalism in patients affected by hypothalamic-pituitary diseases: a retrospective and longitudinal study
    
    ea0110p976
  - Circulating vitamin D levels predict the occurrence of vertebral fractures in patients with cushing's disease
    
    ea0110p977
  - Assessing multiple variables following arginine test enhances the diagnosis of vasopressin deficiency
    
    ea0110p978
  - Cure from acromegaly after long-term medical treatment: may somatostatin receptor ligands drive complete disease disappearance in patients never treated with surgery and/or radiotherapy?
    
    ea0110p979
  - Clinical profile of patients with hypopituitarism in a tertiary endocrine center in nepal
    
    ea0110p980
  - Pituitary apoplexy: a retrospective study of 48 patients from a tertiary endocrine center
    
    ea0110p981
  - Effectiveness of serial prolactin measurement in the subsequent detection of pituitary lesions
    
    ea0110p982
  - Hyperprolactinemia in children and adolescents: clinical characteristics and etiological spectrum
    
    ea0110p983
  - Improving tumour localisation in cushing's disease: synergistic use of 11c-methionine pet/ct and osilodrostat
    
    ea0110p984
- Reproductive and Developmental Endocrinology
- - Reproductive hormones in infertile men with Y chromosome microdeletions
    
    ea0110p26
  - Apoptosis markers and hormonal changes in male infertility
    
    ea0110p27
  - Immune protein profiling of polycystic ovary syndrome
    
    ea0110p985
  - The effect of testosterone on gene expression in muscle in klinefelter syndrome - a single nucleus RNA sequencing study
    
    ea0110p986
  - Exploring the relationship between sex hormones and abdominal muscle composition in postmenopausal women: insights from the multi-ethnic study of atherosclerosis
    
    ea0110p987
  - High risk of type 2 diabetes in klinefelter syndrome irrespective of hypogonadism and testosterone replacement therapy
    
    ea0110p988
  - Precocious puberty and risk of psychiatric disorders: a nationwide register-based cohort study
    
    ea0110p989
  - Liquid chromatography-tandem mass spectrometry (LC-MS/MS) reliability compared to immunometric assay (IA) for testosterone (T) assay in a clinical laboratory setting for male hypogonadism management
    
    ea0110p990
  - Girls with high hormonal steroids, BMI and stress reach puberty early
    
    ea0110p991
  - Modelling polycystic ovary syndrome in vitro with endometrium epithelial organoids and stroma cell culture
    
    ea0110p992
  - Unveiling the genetic architecture of testicular volume: a population-based GWAS using machine learning-based mri segmentations
    
    ea0110p993
  - Changes in circulating small non-coding RNAs after castration
    
    ea0110p994
  - Maternal urinary paracetamol is associated with reduced uterine size and breast tissue diameter at infancy: a COPANA cohort study of 302 healthy girls
    
    ea0110p995
  - Central precocious puberty in males, whether GnRH analog-treated or untreated, is not associated with fertility or general health problems in mid-adulthood
    
    ea0110p996
  - Testosterone to estradiol ratio in men with acute coronary syndrome
    
    ea0110p999
  - New era: the pioneering journey of the GloBE-Reg database of long-acting growth hormone in china
    
    ea0110p1000
  - The Effects of isotretinoin on male reproduction
    
    ea0110p1001
  - Childhood gonadectomy in ireland in differences of sex development (DSD)/intersex: clinical characteristics, historical and current practices, and incidence of gonadoblastoma
    
    ea0110p1002
  - Testicular index: a simple, clinically applicable tool to predict pregnancy outcomes in men with idiopathic infertility undergoing follicle-stimulating hormone treatment
    
    ea0110p1003
  - Puberty induction in adolescents with primary ovarian failure: a single center study over a 10-year period
    
    ea0110p1004
  - Risk of advanced chronic kidney disease in transgender individuals undergoing gender-affirming hormone therapy compared with the general population
    
    ea0110p1005
  - Oligogenicity associated with the adrenal phenotype of individuals with NR5A1/SF-1 variants
    
    ea0110p1006
  - Reproductive hormones at 7-10 years of age in children born after assisted reproductive technology
    
    ea0110p1007
  - Habitual activity and muscle strength in children of mothers with, or without, polycystic ovary syndrome
    
    ea0110p1008
  - Childhood body mass index trajectories in women diagnosed with polycystic ovary syndrome
    
    ea0110p1009
  - Inflammatory stress in leydig cells: implications for steroidogenesis and mitochondrial dysfunction
    
    ea0110p1010
  - Gonadectomy in individuals with differences of sex development - a two year prospective i-dsd registry study
    
    ea0110p1011
  - Changes in reproductive hormones in the years before diagnosis of testicular cancer
    
    ea0110p1012
  - Effects of selected pre-treatments prior to denosumab administration on germ cell proliferation in ex vivo cultured testicular tissue from humanized RANKL mice
    
    ea0110p1013
  - Hypophosphatemia is a frequent finding in infertile men and is associated with semen quality
    
    ea0110p1014
  - Changes in quality of life and intimate experience after 10 years in young women with mayer-rokitansky-kuster-hauser syndrome
    
    ea0110p1015
  - Inhibin b- an important marker to screen testicular function in CAIS patients?
    
    ea0110p1016
  - The effect of treatment on matrix metalloproteinases levels and endothelial function in women with polycystic ovary syndrome. association with metabolic and hormonal abnormalities of the syndrome
    
    ea0110p1017
  - Sex steroids measurement by immunometric assay (IA) compared to liquid chromatography-tandem mass spectrometry (LC-MS/MS) in patients with klinefelter syndrome (KS)
    
    ea0110p1018
  - Exposure to high anti-mullerian hormone (AMH) levels during mini-puberty in mice induces polycystic ovary syndrome-like defects in both sexes
    
    ea0110p1019
  - Visfatin (Nampt) siRNA induced knockdown effect on blastocyst transcriptome, implantation rate and offspring ovarian function. Studies on normal weight and obese mice
    
    ea0110p1020
  - Fibrosis is an early marker of subcutaneous adipose tissue dysfunction in polycystic ovary syndrome (PCOS)
    
    ea0110p1021
  - TSH concentration does not affect metabolic and reproductive hormones in euthyroid women with pcos
    
    ea0110p1022
  - Remission of polycystic ovary syndrome based on the recovery of ovarian morphology identified by three-dimensional power doppler ultrasonography:a retrospective cohort study
    
    ea0110p1023
  - Paternal use of paracetamol prior to conception is associated with elevated adrenal steroid levels in female infants - a copana study
    
    ea0110p1024
  - Outcomes and fertility in men with PAIS worldwide: lessons from an I-DSD registry platform cohort
    
    ea0110p1025
  - Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants
    
    ea0110p1026
  - Low detransition rates among 709 gender-affirming therapy recipients and associated risk factors: results from a systematic follow-up study
    
    ea0110p1027
  - Prevalence and predictive factors of bleeding disorders in adolescents with abnormal uterine bleeding
    
    ea0110p1028
  - Reference intervals for serum total testosterone, free testosterone and sex hormone binding globulin in middle-aged men; the impact of overweight and obesity
    
    ea0110p1029
  - Sleep disturbances in adolescents with PCOS: does metabolic status have an impact beyond obesity?
    
    ea0110p1030
  - Baseline obesity classifications influence the impact of pharmacotherapy on weight and BMI in adolescents with PCOS: findings from the clinical adolescent polycystic ovary (CALICO) database
    
    ea0110p1031
  - Effects of testosterone treatment on the morphology of female internal genitalia assessed by transabdominal ultrasound (TAUS) in trans boys
    
    ea0110p1032
  - Long-term cardiovascular risk in women with subfertility: systematic review and meta-analysis
    
    ea0110p1033
  - Genetic landscape and clinical spectrum of 46,XY differences of sex development: a retrospective study in a major saudi referral center
    
    ea0110p1034
  - Mini-puberty induction in male infants with congenital hypogonadotropic hypogonadism: a case series
    
    ea0110p1035
  - The global landscape of managing hypogonadotropic hypogonadism in male infants: results of an international survey
    
    ea0110p1036
  - A novel role of pregnancy-specific glycoprotein 1 in the maintenance of human chorionic gonadotropin secretion in human placental trophoblasts
    
    ea0110p1037
  - Follicular fluid from women with polycystic ovary syndrome and obesity impairs granulosa cell glycolytic function
    
    ea0110p1038
  - The triglyceride-glucose (TyG) index and its relation to metabolic indices in women with PCOS: a phenotype-based analysis
    
    ea0110p1039
  - Morphometric and transcriptomic changes during early testicular development in pigs
    
    ea0110p1040
  - "Variable phenotypic expression of NR5A1 mutation in a family: sex development abnormalities and management challenges"
    
    ea0110p1041
  - Evidence for bone marrow adipose tissue dysfunction in polycystic ovary syndrome (PCOS)
    
    ea0110p1042
  - PCOS in adolescent girls vs young women: similar distribution of body fat, different severity of PCOS phenotype
    
    ea0110p1043
  - Health behaviours in women conceiving by medically assisted reproduction vs natural conception: a cross-sectional study of 23,334 nulliparous women
    
    ea0110p1044
  - Combining machine learning and metabolomics to identify the metabolic signatures of polycystic ovary syndrome patients according to body mass index
    
    ea0110p1045
  - Detection of piRNA-associated proteins as a diagnostic tool for spermatogenic arrest
    
    ea0110p1046
  - Sexual health in women with type 1 diabetes - a qualitative study from the ReproDia study
    
    ea0110p1047
  - A novel variant in the NDNF gene in a 17-year old boy with hypogonadotropic hypogonadism and anosmia
    
    ea0110p1048
  - Testicular parenchyma inhomogeneity is a potential new marker for testicular dysfunction and subfertility in men born with hypospadias
    
    ea0110p1049
  - The impact of organ specific autoimmunity on menopause onset in females with Graves' disease
    
    ea0110p1050
  - Luteinizing hormone/choriogonadotropin receptor (LHCGR)/G protein-coupled estrogen receptor (GPER) heteromers do not modulate reproductive signals in male and female gonadal cells
    
    ea0110p1052
  - A case of syndromic sexual dysgenesis caused by DAX1 gene duplication
    
    ea0110p1053
  - Follow-up of the pearl cycle app-evaluation: an integrated ovulation prediction kit (OPK) with urine test strips. fertility characteristics, number and course of pregnancies observed
    
    ea0110p1054
  - Late bedtime was associated with increased androgen and reduced lean mass in women with polycystic ovary syndrome: a cross-sectional study
    
    ea0110p1055
  - Impaired sperm quality in previous illicit users of anabolic androgenic steroids
    
    ea0110p1056
  - Establishing mouse ovarian ex vivo tissue culture
    
    ea0110p1057
  - The impact of estrogens on gut microbiome in post-menopause and premature ovarian insufficiency - a meta-analysis and systematic review
    
    ea0110p1058
  - Health implications of self-reported PCOS in a developing country: the brazilian longitudinal study of adult health
    
    ea0110p1059
  - Clinical and genetic overlap between congenital hypogonadotropic hypogonadism and cleft lip and palate
    
    ea0110p1060
  - Opposite degrees of virilisation in two individuals with 46,XY DSD and variants in NR5A1/SF1
    
    ea0110p1061
  - Reevaluating reference intervals for androstenedione in reproductive-aged woman
    
    ea0110p1062
  - Follicular fluid from women with polycystic ovary syndrome affects negatively the progressive motility of capacitating human spermatozoa
    
    ea0110p1063
  - Perfluorooctanoic acid (PFOA) and male reproductive health: redox status imbalance in Wistar rat testes
    
    ea0110p1064
  - What matters most? gender diverse individuals' perspective in gender-affirming hormone therapy - the TRANSFORM study
    
    ea0110p1065
  - Hair mercury levels in children with central precocious puberty and healthy individuals from two distinct geographic regions of Brazil
    
    ea0110p1066
  - Establishment of a foetal and prepubertal testis ex vivo mouse model
    
    ea0110p1067
  - Neurocognitive function in males with 46,XX testicular disorder of sex development
    
    ea0110p1068
  - Polycystic ovary syndrome in adolescent females with type 1 diabetes: a gonadotropins, leptin, insulin interplay
    
    ea0110p1069
  - Characterisation and evaluation of models of care for polycystic ovary syndrome (PCOS): a multinational study on clinical features, screening practices, and treatment outcomes
    
    ea0110p1070
  - Association of insulin resistance surrogate indices and erectile dysfunction: a systematic review and meta-analysis
    
    ea0110p1071
  - Identification of two novel likely pathogenic NR5A1 variants associated with DSD and infertility in two Kuwaiti families
    
    ea0110p1072
  - Disorders of sex development due to 17sz-hydroxysteroid dehydrogenase type 3 deficiency: searching for a phenotype-genotype correlation
    
    ea0110p1073
  - A case of 46, XY complete gonadal dysgenesis presenting with precocious peripheral puberty
    
    ea0110p1074
  - Testicular growth and sperm detection rates following combined hcg and rfsh therapy in adolescents with congenital and acquired hypogonadotropic hypogonadism
    
    ea0110p1075
  - Multilingual menopause comics: combating misinformation and enhancing global health literacy through peer-reviewed educational videos
    
    ea0110p1076
  - Role of anti-TPO antibodies on ovarian reserve and early embryo development in assisted reproductive technology
    
    ea0110p1077
  - Body composition and bone mineral density in adolescents with gender incongruence
    
    ea0110p1078
- Thyroid
- - Familial papillary thyroid carcinoma: identification of 12 families and novel putative gene defects in the finnish population
    
    ea0110p28
  - THRIVE-2 phase 3 trial of Veligrotug (VRDN-001) in chronic thyroid eye disease (TED): efficacy and safety at 15 weeks
    
    ea0110p29
  - Atypia of undetermined significance (AUS) in pediatric thyroid nodules: Surgery after first fine needle aspiration (FNA) or follow-up?
    
    ea0110p30
  - Diving into the shared genetics between hypothyroidism and its co-morbidities: Multi-trait meta-analyses and gene prioritization provide novel insights into the common genetic and biological factors
    
    ea0110p1080
  - Epithelial and tumor microenvironment changes driven by BRAF/RAS mutations in thyroid cancer progression
    
    ea0110p1081
  - Thyroid eye disease: online medical education unveils knowledge gaps and barriers regarding targeted immunotherapy
    
    ea0110p1082
  - Mental health, anxiety, depression, and the risk of incident thyroid dysfunction
    
    ea0110p1083
  - Thyroid function and ultrasound morphology of the thyroid gland in a cohort of patients with rasopathies: an italian multicenter study
    
    ea0110p1084
  - Fatal carotid blowout syndrome induced by lenvatinib and nivolumab combination therapy in anaplastic thyroid cancer: a case report
    
    ea0110p1085
  - Timing of levothyroxine ingestion in the INFINITY-study: a randomized controlled trial comparing dose-adjusted, non-fasting and fasting levothyroxine ingestion
    
    ea0110p1086
  - Natural course of subclinical hyperthyroidism in primary care in the netherlands
    
    ea0110p1087
  - Trends in thyroid cancer in the balearic islands, insights from 2000 - 2020 to 2021 - 2023
    
    ea0110p1088
  - Levothyroxine use in Belgium in 2003-2020: a longitudinal population-level registry-based cohort analysis
    
    ea0110p1089
  - Paediatric thyroid cancer management in france: a TUTHYREF network
    
    ea0110p1090
  - Is postoperative radioactive iodine (RAI) ablation necessary for low- and low-to-intermediate-risk papillary thyroid carcinomas? a web survey among Greek endocrinologists
    
    ea0110p1091
  - Artificial Intelligence-based longitudinal analyses of hypothyroidism patients using data from electronic health records provide insights into the sex-specific patient cluster patterns
    
    ea0110p1092
  - Molecular characterization of a multicenter cohort of patients with non-autoimmune subclinical hypothyroidism
    
    ea0110p1093
  - Evaluation of the diagnostic accuracy of European and ACR-TIRADS classification systems for thyroid nodules exceeding 20 mm in diameter
    
    ea0110p1094
  - Radiofrequency ablation (RFA) for locoregional structural incomplete response (SIR) in differentiated thyroid cancer (DTC)
    
    ea0110p1095
  - Clinical characteristics and outcomes of graves' disease in patients with prior hypothyroidism
    
    ea0110p1096
  - Biological activity and therapeutic potential of SAFA-based long-acting rhTSH
    
    ea0110p1097
  - Washout CYFRA 21-1 as a biomarker for thyroid cancer diagnosis in thyroid nodules
    
    ea0110p1098
  - Combining TERT promoter mutations with american thyroid association risk stratification system to predict short-term prognosis in papillary thyroid carcinoma
    
    ea0110p1099
  - Circulating tumor DNA as a diagnostic marker for molecular alterations in anaplastic thyroid cancer using next generation sequencing
    
    ea0110p1100
  - Differentiated thyroid carcinomas and its pre-operative characterization: a single centre study
    
    ea0110p1101
  - Clinical outcomes of non-invasive follicular thyroid neoplasm with papillary-like nuclear features: a single-center experience
    
    ea0110p1102
  - Hemithyroidectomy vs. total thyroidectomy for low-risk differentiated thyroid carcinoma: a retrospective cohort study from romania
    
    ea0110p1103
  - Evaluation of the role of systemic immune-inflammatory markers in predicting malignancy in patients with thyroid nodules
    
    ea0110p1104
  - Discordant thyroid function tests - a case report of ewly identified rare mutation of transthyretin related euthyroid hyperthyroxinaemia
    
    ea0110p1106
  - Endocrine specialist nurse-led post-radioiodine care pathway improves patient outcomes
    
    ea0110p1107
  - New de novo variants in THRA gene in adolescent patients: two clinical cases
    
    ea0110p1108
  - Parathyroid cyst in an adolescent girl - a rare pathology in pediatric population
    
    ea0110p1109
  - Preoperative detection of pathogenic variants in children and adolescents
    
    ea0110p1110
  - Efficacy and safety of the FCRN inhibitor, batoclimab, in graves' thyroidal and extrathyroidal disease: a proof-of-concept study
    
    ea0110p1111
  - Thyroglobulin antibodies in patients with thyroid cancer: autoimmunity or cancer immunoediting?
    
    ea0110p1112
  - Afirma genomic classifier in clalit health services: preserving thyroids and promoting equality
    
    ea0110p1113
  - The increased coexistence of autoimmune thyroid disease (AITD) in children and adolescents with differentiated thyroid carcinoma (DTC) in years 2015-2024 compared to 1996-2000; one center experience
    
    ea0110p1114
  - Total thyroidectomy vs thyroid lobectomy for low-risk papillary thyroid cancer
    
    ea0110p1115
  - Rituximab in addition to methylprednisolone pulse therapy for graves' orbitopathy improves the remission of graves' hyperthyroidism
    
    ea0110p1117
  - The role of blood cell derived parameters in the differential diagnosis of subacute thyroiditis and Graves' disease and long-term outcomes in subacute thyroiditis: a tertiary center experience
    
    ea0110p1118
  - The association between subcategorization, cytomorphological features, ultrasonographic characteristics, ACR and EU-TIRADS classifications with surgical outcomes of aus nodules
    
    ea0110p1119
  - Fear of recurrence in thyroid papillary cancer: a risk based comparison
    
    ea0110p1120
  - A case of pendred syndrome presenting due to thyroid nodule
    
    ea0110p1121
  - Predictors of initial remission in patients treated with antithyroid drugs for graves' disease
    
    ea0110p1122
  - Extracellular vesicles as a novel immunotherapeutic strategy in hashimoto's thyroiditis: advances in targeted delivery technologies
    
    ea0110p1123
  - CD74+ thyrocytes in hashimoto's thyroiditis: a potential therapeutic approach
    
    ea0110p1124
  - Method related differences in fT4 immunoassays are marked in the hyperthyroid range and support the need for assay standardisation
    
    ea0110p1125
  - Thyroid nudules in girls with mccune-albright syndrome(MAS) and gnrh independent precocious puberty concurrently
    
    ea0110p1126
  - Re-emergence of iodine deficiency-induced thyroid disorders in children: a comprehensive review and meta-analysis
    
    ea0110p1127
  - Genetic characterization of congenital hypothyroidism with gland in situ: findings from a cohort of italian pediatric patients
    
    ea0110p1128
  - Improving hormonal balance in the treatment of pediatric congenital hypothyroidism: the role of combined LT4-LT3 therapy
    
    ea0110p1129
  - Metabolic dysfunction-associated steatotic liver disease and the risk of thyroid cancer: a complication of systemic metabolic disorder
    
    ea0110p1131
  - Grave's orbitopathy: an atypical presentation
    
    ea0110p1132
  - Management of low-risk differentiated thyroid carcinomas in nuclear medicine: a retrospective study of 280 cases
    
    ea0110p1133
  - A study on the correlation between hyperthyroidism and bone metabolism & bone mass in children
    
    ea0110p1134
  - Levothyroxine absorption test with daily levothyroxine dose: preliminary results in patients with refractory hypothyroidism
    
    ea0110p1135
  - Familial thyroid hormone resistance: a case series of two sisters with THRsz mutation
    
    ea0110p1136
  - Differentiated thyroid cancer in acromegaly: increased risk, unaltered outcomes
    
    ea0110p1137
  - Association of extra-thyroidal abnormalities and genetic variants in congenital hypothyroidism: a single-centre study
    
    ea0110p1138
  - Chronotype and daytime sleepiness in patients with hashimoto's thyroiditis
    
    ea0110p1139
  - miRNA expression profiles in thyroid tumors with nras q61r variant
    
    ea0110p1140
  - Unraveling clinical clues for deciphering thyroid nodule malignancy
    
    ea0110p1141
  - Differences between pediatric and adult treatment protocols in differentiated thyroid carcinoma: need for transitional guidelines for adolescents
    
    ea0110p1142
  - A novel biallelic intronic variant in the TG gene associated with thyroid dyshormonogenesis and fetal goiter
    
    ea0110p1143
  - Antithyroid drug therapy for pediatric graves' disease: a dose-effect relationship study of initial dose and short-term efficacy
    
    ea0110p1144
  - miRNA expression profiles in braf v600e positive thyroid tumors
    
    ea0110p1145
  - miRNA expression profiles in medullary thyroid carcinoma with HRAS Q61R variant
    
    ea0110p1146
  - The impact of dry eye disease on magnetic resonance imaging findings and quality of life in patients with graves' orbitopathy
    
    ea0110p1147
  - Risk of psychiatric disorders in patients with graves' disease: a nationwide population-based analysis
    
    ea0110p1148
  - Simultaneous occurrence of subacute thyroiditis and graves' disease
    
    ea0110p1149
  - Angioinvasion and multifocality in papillary thyroid cancer: identifying prognostic biomarkers
    
    ea0110p1150
  - C cell hyperplasia and multifocal papillary thyroid microcarcinoma in a patient with remarkably elevated basal and stimulated calcitonin levels
    
    ea0110p1151
  - Re-considering wolff chaikoff effect in paediatrics
    
    ea0110p1152
  - Variable phenotype of resistance to thyroid hormone due to a pathogenic THRA gene variant in a mother and her two daughers
    
    ea0110p1153
  - Hidden impact of high-dose hook effect: a case report on cross-reactivity of human chorion gonadotropin on thyroid function
    
    ea0110p1154
  - Clinical profile and incidence of childhood graves' disease in brunei darussalam
    
    ea0110p1155
  - Visual functioning and physical appearance quality of life (QoL) scores of Thyroid Eye Disease (TED) patients seen in a multidisciplinary consultation
    
    ea0110p1156
  - Iron deficiency and thyroid dysfunction: impact of iron supplementation on tsh levels in women of reproductive age in ajara georgia
    
    ea0110p1157
  - Antithyroid arthritis syndrome in pediatric graves' disease: a rare adverse methimazole reaction
    
    ea0110p1158
  - AI-driven EMR integration in functional thyroid dysfunction: advancing diagnosis and management
    
    ea0110p1159
  - Utility of sPD-l1 and sPD-1 as biomarkers for assessing clinical activity in moderate-to-severe thyroid eye disease
    
    ea0110p1160
  - Microwave ablation therapy of an intrathyroid parathyroid adenoma
    
    ea0110p1161
  - A multimodal large language model as an end-to-end classifier of thyroid nodule malignancy risk: practical or potential?
    
    ea0110p1162
  - Thyroid artery embolization for compressive goiter in high surgical risk patients
    
    ea0110p1163
  - A case of autonomous hot thyroid nodule
    
    ea0110p1164
  - Evaluation of the effects of antithyroid drug therapy on body mass index in children and adolescents with graves' disease
    
    ea0110p1165
  - Evaluation of ultrasonographic and clinicopathological features of gallium-68 DOTA-TATE uptake in the thyroid gland
    
    ea0110p1166
  - Lymph node ratio predicts persistence/recurrence in medullary thyroid cancer
    
    ea0110p1167
  - Clinicopathological evaluation of advanced thyroid cancer
    
    ea0110p1168
  - Thyrotoxic hypokalaemia periodic paralysis-
    
    ea0110p1169
  - Radioiodine therapy in pediatric graves' disease: insights from a single-center study of 35 cases
    
    ea0110p1170
  - miRNA expression in the thyroid tumors with HRAS Q61R pathogenic variant
    
    ea0110p1171
  - Laboratory patterns differ between patients with severe vs milder forms of congenital hypothyroidism
    
    ea0110p1172
  - Thyroid nodule of tuberculous origin: a delayed and unexpected diagnosis - a case report
    
    ea0110p1173
  - Neuropsychological and growth outcomes in congenital hypothyroidism: impact of timing of thyroid hormone supplementation
    
    ea0110p1174
  - Prevalence of hypothyroidism in children with nephrotic syndrome: a systematic review and meta-analysis
    
    ea0110p1175
  - OCT and OCTA evaluation of neurovascular structures in pediatric graves' disease without active ophthalmopathy
    
    ea0110p1176
  - Thyroid lymphoma presented as a painful cervical mass: a diagnostic dilemma
    
    ea0110p1177
  - The impact of levothyroxine treatment on T lymphocyte gene expression in Hashimoto's thyroiditis
    
    ea0110p1178
  - Diagnostic performance of ultrasound-based risk stratification systems for follicular thyroid carcinoma
    
    ea0110p1179
  - The coexistence of graves' disease and thymic hyperplasia: a case report
    
    ea0110p1180
  - Case report: misleading increase in thyroid-stimulating hormone receptor antibodies during pregnancy in graves disease: value of functional, cell-based assays
    
    ea0110p1181
  - Thyroid dysfunction in children with nephropathic cystinosis- single center experience
    
    ea0110p1182
  - Risk factors, clinical characteristics, and outcomes of pediatric thyroid cancer: an egyptian single center experience
    
    ea0110p1183
  - Spindle epithelial tumor with thymus-like differentiation: A rare thyroid entity
    
    ea0110p1184
  - Using TSH-receptor antibody testing to guide antithyroid drug withdrawal reduces the early relapse rate - a population-based study
    
    ea0110p1185
  - Trapping-only nodules - are they higher risk for malignancy?
    
    ea0110p1186
  - From thyroid storm to cardiac recovery: the impact of hyperthyroidism on heart function
    
    ea0110p1187
  - Decoding elevated tsh with normal free t4: a comprehensive guide to differentiation, genetic insights, and diagnostic strategies
    
    ea0110p1188
  - Ultrasonography and cytology previous results analysis in patients that have undergone thyroid surgery
    
    ea0110p1189
  - Thyroid peroxidase antibodies and their role in predicting outcomes in graves' disease treatment
    
    ea0110p1190
  - Admission and follow-up characteristics of pediatric and adolescent patients with hyperthyroidism
    
    ea0110p1191
  - Hyperthyroidism and renal function: unravelling the diagnosotic dilemma in GFR estimation
    
    ea0110p1192
  - Life saving Plasma exhchange in resistant thyroid storm with myocardial infacrtion
    
    ea0110p1193
  - Thyroid cancer in thyroglossal duct cysts
    
    ea0110p1194
  - Predictor of treatment outcome for pediatric Grave's disease
    
    ea0110p1195
  - Prevalence of thyroid dysfunction in children with asthma in a tertiary care hospital of jharkhand, india - a cross-sectional study
    
    ea0110p1197
  - Thyroid cancer in children: insights from an 18-year retrospective study at a tertiary center
    
    ea0110p1198
  - Genetic landscape of goiterous hypothyroidism: key markers and clinical insights
    
    ea0110p1199
  - Ultrasound-based ultra-micro angiography for evaluating vascularity in diffuse thyroid disorders
    
    ea0110p1200
  - A less known cause of orbitopathy
    
    ea0110p1202
  - An optimal capillary screen cut-off of thyroid stimulating hormone for diagnosing congenital hypothyroidism: gathering evidence
    
    ea0110p1203
  - Nationwide web-survey on implementing the 2023 ETA guidelines for thyroid nodule management
    
    ea0110p1205
  - Riedl's thyroiditis arising from stable chronic atrophic Hashimoto's thyroiditis
    
    ea0110p1206
  - The clinical impact of vitamin D supplementation on thyroid eye disease outcome
    
    ea0110p1207
  - Association of thyroid cancer risk with plasma 25-hydroxyvitamin D levels in multinodular goiter patients
    
    ea0110p1208
  - MCT8 deficiency - a pathway of the "floppy baby" from thyroxine treatment to tiratricol
    
    ea0110p1209
  - A report on an unusual source of heterophilic antibodies interfering with thyroid function tests
    
    ea0110p1210
  - Challenges in the treatment and long-term follow-up results of children with resistance to thyroid hormone-sz
    
    ea0110p1211
  - A decade of thyroid orbitopathy research in albania: a retrospective study from a tertiary referral center
    
    ea0110p1212
  - Children undergoing thyroid surgery - diagnostic evaluation, type of surgery and pathological findings
    
    ea0110p1213
  - Congenital central hypothyroidism due to TSHB gene mutation: a case report
    
    ea0110p1214
  - Sonographic evaluation of thyroid volume and morphology over time in children with hashimoto's thyroiditis
    
    ea0110p1215
  - Clinical audit on ultrasound assessment and thyroid function testing in evaluation of thyroid nodules in a regional centre in Ireland
    
    ea0110p1216
  - Ultrasound-guided thermal ablation of symptomatic benign thyroid nodules: volumetric outcomes in a cohort of 36 patients
    
    ea0110p1217
  - Exacerbation of orbitopathy after total thyroidectomy in alemtuzumab-induced graves' disease: a case report
    
    ea0110p1218
  - The relationship between TSH suppression and metabolic associated fatty liver disease (MAFLD) in patients with thyroid cancer
    
    ea0110p1219
  - Complete blood count markers as possible prognostic values of immune checkpoint inhibitors induced hypothyroidism
    
    ea0110p1220
  - The rare entity of de Quervain thyreoiditis can be associated with hepatitis a
    
    ea0110p1221
  - Predictive factors for hypothyroidism in childhood autoimmune thyroiditis: insights from long-term follow-up
    
    ea0110p1222
  - Molecular insights into persistent or residual pediatric differentiated thyroid cancer
    
    ea0110p1223
ePoster Presentations
- Adrenal and Cardiovascular Endocrinology
- - A case of mistaken identity: hypoadrenalism and the cirrhotic paradox
    
    ea0110ep1
  - Effects of switching from conventional glucocorticoid therapy to modified-release hydrocortisone (MR-HC) on the steroid matabolome in patients with 21-hydroxylase deficiency
    
    ea0110ep2
  - Echocardiographic evaluation of functional and morphological alterations in obesity: a comparison between obese individuals with and without Metabolic Syndrome
    
    ea0110ep3
  - Impact of alert systems on glucocorticoid administration for adrenal insufficiency in the emergency department
    
    ea0110ep4
  - -H hormonal profile in patients affected by congenital adrenal hyperplasia: does it improve disease management?
    
    ea0110ep5
  - Suspected central adrenal insufficiency in a patient with PMM2-CDG
    
    ea0110ep6
  - First case of cytochrome P450 oxidoreductase deficiency with didelphic uterus and unilateral renal agenesis and a literature review on 46,XX patients
    
    ea0110ep7
  - Clinical, hormonal, and radiological evaluation of unilateral adrenal incidentalomas
    
    ea0110ep8
  - Heterozygous mutations in CYP11A1 lead to P450scc deficiency: case report and literature review
    
    ea0110ep9
  - Pitfalls of circulating miRNA-based biomarker studies in adrenocortical tumors
    
    ea0110ep10
  - The role of the posture test for primary aldosteronism subtyping
    
    ea0110ep11
  - The hippocampus in congenital adrenal hyperplasia (CAH) and autoimmune Addison's disease (AAD)
    
    ea0110ep12
  - Clinical characteristics of a large single-centre cohort of paediatric patients with congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency
    
    ea0110ep13
  - Management of adrenal insufficiency during pregnancy
    
    ea0110ep14
  - Impact of glucocorticoid replacement therapy on carbohydrate metabolism in patients with Addison disease
    
    ea0110ep15
  - Prognostic factors for survival in patients with metastatic adrenocortical carcinoma
    
    ea0110ep16
  - Continuous glucose monitoring in adult patients with classic congenital adrenal hyperplasia under different glucocorticoid regimens
    
    ea0110ep17
  - Adrenal and peri-adrenal schwannomas: two case reports and a review of clinical, imaging and pathological features
    
    ea0110ep18
  - Secondary adrenal insufficiency and immune checkpoint inhibitors: case series with pembrolizumab from a non-oncologic hospital
    
    ea0110ep19
  - Non-functional retroperitoneal paraganglioma: a case report
    
    ea0110ep20
  - Evaluation of adiponectin level and metabolic parameters in patients with mild autonomous cortisol secretion and non-functional adrenal adenomas
    
    ea0110ep21
  - Integrating patient and public involvement into simulation-based learning: a mixed-methods study enhancing healthcare professionals' confidence in managing adrenal disorders
    
    ea0110ep22
  - Transient 18F-FDG PET/CT uptake of contralateral adrenal gland in patient under Mitotane for R0 corticosurrenaloma
    
    ea0110ep23
  - The novel atherogenic indices and anthropometric measurements in patients with non-functioning adrenal adenomas and cardiovascular disease risk
    
    ea0110ep25
  - Prevalence, value, and reliability of genetic testing in congenital adrenal hyperplasia: a comprehensive review
    
    ea0110ep26
  - Adverse events in heart failure patients on SGLT2 inhibitors: a retrospective study
    
    ea0110ep27
  - Pheochromocytoma-induced takotsubo cardiomyopathy in a patient with SDHA and EGLN1 variants
    
    ea0110ep28
  - Carbohydrate metabolism disorders in pheochromocytoma
    
    ea0110ep29
  - Impact of Covid-19 pandemic on pheochromocytoma and paraganglioma incidence
    
    ea0110ep30
  - Glycemic disorders in pheochromocytoma and paraganglioma
    
    ea0110ep31
  - A case of aldosterone synthase deficiency presenting with hyponatremia in a 17-year-old male
    
    ea0110ep32
  - Congenital adrenal hyperplasia: about 10 cases in burkina faso
    
    ea0110ep33
  - Cell-cell communication shapes the impact of obesity-associated stressors on human vascular cells
    
    ea0110ep34
  - Adrenal incidentalomas and risk for cancer: a monocentric study in a tertiary greek center
    
    ea0110ep35
  - Aspects of diagnosing testosterone-producing tumours
    
    ea0110ep36
  - Primary adrenal lymphoma- 15years retrospective analysis from a tertiary care centre
    
    ea0110ep37
  - Nonsurgical management of pheochromocytoma in the very elderly - a case series and review of the literature
    
    ea0110ep38
  - The necessity for new criteria for overnight dexamethasone suppression test to diagnosis of cushing's syndrome
    
    ea0110ep39
  - From venipuncture to self-sampling DBS: a shift in monitoring testosterone levels
    
    ea0110ep40
  - Targeted proteomics reveals novel biomarkers of disease activity and cardiometabolic risk in acromegaly
    
    ea0110ep41
  - Vitamin D receptor mRNA expression in adrenal medulla and pheochromocytoma cells
    
    ea0110ep42
  - Long-term metabolic comorbidities in patients with adrenal incidentalomas - a single center experience
    
    ea0110ep43
  - Analysis of clinical characteristics and pharmacological treatment to achieve adequate plasma renin activity levels in primary hyperaldosteronism
    
    ea0110ep44
  - cases with different clinical features due to adrenal insufficiency after adrenal hemorrhage in newborns
    
    ea0110ep45
  - Thematic analysis of quality of life in a community-based sample of adults living with congenital adrenal hyperplasia reveals a significant unmet medical need
    
    ea0110ep46
  - Two different clinical presentations, one rare diagnosis: adrenocortical tumor
    
    ea0110ep47
  - A case of glucocorticoid deficiency due to MC2R mutation
    
    ea0110ep48
  - "Adrenal insufficiency with low 17-hydroxyprogresterone: lesson learned from a developing country"
    
    ea0110ep49
  - How to discover non-functioning adrenal cortical adenomas
    
    ea0110ep50
  - A rare case of iatrogenic cushing's syndrome
    
    ea0110ep51
  - A case of concurrent RET and FH GENE mutations in a patient with metastatic pheochromocytoma
    
    ea0110ep52
  - Two decades of ectopic ACTH cushing syndrome: retrospective analysis from a tertiary care centre in north India
    
    ea0110ep53
  - Assessment of atherosclerotic cardiovascular disease (ASCVD) risk using ASCVD risk estimator plus in indian patients with type 2 diabetes - a subgroup analysis from real-world, retrospective study
    
    ea0110ep54
  - Treatment of MACS with low doses of metyrapone - a preliminary report
    
    ea0110ep55
  - The role of a multidisciplinary team in the management of phaeochromocytomas
    
    ea0110ep56
  - Pheochromocytoma and pregnancy: diagnostic challenges and multidisciplinary management
    
    ea0110ep57
  - Incidentaloma: pathological and biochemical analysis management in the disorders of the adrenal medulla in albania popullation
    
    ea0110ep58
  - Stratification of total cardiovascular risk in young patients with type 1 diabetes mellitus
    
    ea0110ep59
  - Pituitary adenomas in adult bulgarian CAH patients
    
    ea0110ep60
  - Multiple recurrent cerebral and coronary vasospasms as an unusual initial presentation of pheochromocytoma: a case report and literature review
    
    ea0110ep61
  - A Chinese case of familial progressive hyperpigmentation and hypopigmentation misdiagnosed as primary adrenal insufficiency
    
    ea0110ep62
  - Evaluation of cardiovascular complications of primary hyperparathyroidism
    
    ea0110ep63
  - Clinical and paraclinical monitoring of pediatric patients with congenital adrenal hyperplasia: challenges and outcomes
    
    ea0110ep64
  - Effects of cushing's Syndrome remission on glycemic control: does remission always lead to improvement
    
    ea0110ep65
  - Infant with pubarche and suppressed serum cortisol. what is the diagnosis?
    
    ea0110ep66
  - Hypovitaminosis D and its association with the incidence and severity of major adverse cardiovascular events
    
    ea0110ep67
  - Significant metabolic syndrome improvement in a patient with adrenal Cushing's syndrome treated preoperatively with osilodrostat
    
    ea0110ep68
  - Mild autonomous cortisol secretion (MACS): data from a romanian tertiary centre
    
    ea0110ep69
  - ESPE caucasus&central asia school (C&CAS) sharing knowledge for saving patients' lives:organizing newborn-screening and pediatric endocrinology care for patients with adrenal insufficiency in armenia
    
    ea0110ep70
  - Primary adrenal insufficiency secondary to bilateral adrenal metastases: can extreme hyponatremia be compatible with life?
    
    ea0110ep71
  - Evaluation of bilateral adrenal incidentaloma at an endocrine department in Tunisia
    
    ea0110ep72
  - An adolescent-onset case of X-linked adrenoleukodystrophy with diagnostic challenges
    
    ea0110ep73
  - Pheochromocytomas and paragangliomas: clinical presentation, management, and outcomes in a tunisian cohort
    
    ea0110ep74
  - Prevalence, clinical and laboratory features of pheochromocytoma in minsk residents: analysis of data for 2023
    
    ea0110ep75
  - -hydroxilase autoantibodies positivity in Bulgarian patients with addison's disease and premature ovarian failure
    
    ea0110ep76
  - Reversion of impaired glucose tolerance and diabetes in patient with primary hyperaldosteronism -case report
    
    ea0110ep77
  - Uncharted territory: a novel SDHC mutation in a young patient with paraganglioma
    
    ea0110ep78
  - Cyclical cushing's syndrome secondary to ectopic ACTH-secreting neuroendocrine tumor: a diagnostic and therapeutic challenge
    
    ea0110ep79
  - Incidental adrenal mass leading to diagnosis of a rare composite pheochromocytoma
    
    ea0110ep80
  - ACTH-independent cushing's disease due to macronodular hyperplasia with a late diagnosis of klinefelter's syndrome
    
    ea0110ep81
  - Age-related differences and machine learning- based insights in patients with non-functioning adrenal adenomas
    
    ea0110ep82
  - Exploring the role of bilateral adrenalectomy in pediatric cushing's syndrome: case series and literature review
    
    ea0110ep83
  - Aldosteronproducing adrenal oncocytoma
    
    ea0110ep84
  - Adult onset of X-linked adrenoleukodystrophy: insights from a unique case
    
    ea0110ep85
  - Adrenergic crises simulating severe cardiac pathology
    
    ea0110ep86
  - Preparation for adrenal cortical carcinoma surgery with injectable fluconazole, a second successful experience (case report)
    
    ea0110ep87
  - Diagnosis of pheochromocytoma in a patient with recurrent reverse takotsubo cardiomyopathy
    
    ea0110ep88
  - The combination of afternoon and midnight salivary cortisol improves the diagnosis of cushing's syndrome
    
    ea0110ep89
  - Adrenal tuberculosis has not revealed all its secrets:an unusual case
    
    ea0110ep90
  - Post operative hypoaldosteronism after unilateral adrenalectomy. a case report and review of the literature
    
    ea0110ep91
  - Congenital adrenal hyperplasia and addison's disease: coincidence or consequence?
    
    ea0110ep92
  - How early should screening be performed in patients with congenital adrenal hyperplasia?
    
    ea0110ep93
  - Non-arteritic anterior ischemic optic neuropathy and addison's disease
    
    ea0110ep94
  - Skin lightening cream causing hypoadrenalism
    
    ea0110ep95
  - Thyroid hormone resistance syndrome de novo in a patient with THR mutation c.749T>C. a case report
    
    ea0110ep96
  - Ectopic ACTH syndrome in a patient with pheochromocytoma
    
    ea0110ep97
  - Acute hypoglycemia after surgery - a clue for the diagnosis of adrenal insufficiency
    
    ea0110ep98
  - Composite adenomatoid tumor with myelolipoma of adrenal gland: case report
    
    ea0110ep99
  - Neurofibromatosis type 1 with pheochromocytoma with high potential for progression (clinical case)
    
    ea0110ep100
  - Carotid paraganglioma: About 4 cases
    
    ea0110ep101
  - A rare case of codeine-induced secondary adrenal insufficiency with hyponatremia worsened by hydrochlorothiazide: a case report and review of literature
    
    ea0110ep102
  - Unmasking the genetics: decoding the paternal code in pheochromocytomas
    
    ea0110ep103
  - Adrenal suppression secondary to intranasal corticosteroid use: a case report
    
    ea0110ep104
  - Giant bilateral myelolipomas in a female patient with untreated classic 21-hydroxylase deficiency: a case report
    
    ea0110ep105
  - Achieving spontaneous pregnancy in a patient with classic congenital adrenal hyperplasia through modified-release hydrocortisone
    
    ea0110ep106
  - Bilateral macronodular adrenal cortical disease: a case series
    
    ea0110ep107
  - A patient with pheochromocytoma and MDH2 variant (c.478G>A)
    
    ea0110ep108
  - Amiodarone-induced thyrotoxicosis type 2 and iatrogenic cushing syndrome in patient with advanced heart failure and left ventricular assist device
    
    ea0110ep109
  - Case report: trauma - induced adrenal hematoma and pseudopheochromocytoma phenomenon
    
    ea0110ep110
  - Unfavorable metabolic outcomes in pediatric patients with classic congenital adrenal hyperplasia - study method proposal
    
    ea0110ep111
  - CAH care in a district general setting: care, safety and preferences
    
    ea0110ep112
  - Essential hypertension or primary hyperaldosteronism? Detecting the undetectable
    
    ea0110ep113
  - Non-functioning adrenal cortical adenomas: analysis of 31 cases
    
    ea0110ep114
  - Biochemically negative retroperitoneal paraganglioma: a case report
    
    ea0110ep115
  - Osilodrostat as a bridge to surgery in patient with ectopic cushing's syndrome
    
    ea0110ep116
  - Unusual adrenal incidentaloma: the ganglioneuroma
    
    ea0110ep117
  - Stage IV lung cancer with metastases confined to the adrenal glands: a case report
    
    ea0110ep118
  - Bilateral carotid paraganglioma: a rare entity
    
    ea0110ep119
  - Imaging phenotype over size: two cases of cavernous hemangiomas of the adrenal glands
    
    ea0110ep120
  - A rare case of silent metastatic pheochromocytoma with a breast metastasis
    
    ea0110ep121
  - "Adrenal incidentaloma complicated by adrenal crisis in a critically ill patient "- a case report
    
    ea0110ep122
  - A study on incidence and related characteristics of PPGLs in a well-defined population
    
    ea0110ep123
  - Addison's disease initially interpreted as sarcoidosis
    
    ea0110ep124
  - Is adrenalectomy still required as a treatment in cushing disease?
    
    ea0110ep125
  - Prevalence and evolution of diabetes in cushing's syndrome: a 31-year retrospective study
    
    ea0110ep126
  - Impact of cushing's syndrome treatment on glycemic control and diabetic complications
    
    ea0110ep127
  - Factors influencing persistence of diabetes after cushing's syndrome remission
    
    ea0110ep128
  - Diabetes in cushing's syndrome: secondary or type 2 diabetes
    
    ea0110ep129
  - Rare association of primary hyperaldosteronism and cushing's syndrome: clinical, hormonal, and imaging insights from a case series
    
    ea0110ep130
  - Overcoming the challenge: weaning corticosteroids in glucocorticoid-induced adrenal insufficiency
    
    ea0110ep131
  - Asymptomatic giant cystic pheochromocytoma, a misleading entity: a case report
    
    ea0110ep132
  - Clinical audit of outpatient short synacthen test utilisation and outcomes in a tertiary care cohort
    
    ea0110ep133
  - Primary hyperaldosteronism: diagnostic approach (endocrine-radiological)
    
    ea0110ep134
  - Implications of new diagnosis of adrenal insufficiency on class 1 commercial pilot licence
    
    ea0110ep135
  - Adrenal tumor in a child with salt-wasting 21-hydroxylase deficiency congenital adrenal hyperplasia
    
    ea0110ep136
  - Outcomes of bilateral adrenalectomy in patients with severe and persistent cushing's disease: a case series
    
    ea0110ep137
  - Adrenal schwannoma: a case report
    
    ea0110ep138
  - Silent pheochromocytoma: an insidious surgical finding
    
    ea0110ep139
  - Ganglioneuroma in a patient with primary adrenal insufficiency: a case report
    
    ea0110ep140
  - Acromegaly and high-grade heart blocks: a rare situation
    
    ea0110ep141
  - Not your average cushing syndrome - a case with a series of unusual complications
    
    ea0110ep142
  - Glycemic control and cortisol levels in patients with cushing's syndrome
    
    ea0110ep143
  - Adrenal ganglioneuroma: a rare mass and diagnostic challenge
    
    ea0110ep144
  - Familial form of adrenoleukodystrophy with late diagnosis of chronic adrenal insufficiency (clinical case)
    
    ea0110ep145
  - A challenging diagnosis in a patient with primary adrenal insufficiency
    
    ea0110ep146
  - Case of spontaneous adrenal tumour infarction resembling pheochromocytoma
    
    ea0110ep147
  - Prepubertal gynecomastia in a boy with classic 21-hydroxylase deficiency
    
    ea0110ep148
  - Adrenal imaging pitfalls: a case of a giant renal liposarcoma mimicking an adrenal tumor
    
    ea0110ep149
  - Primary adrenal insufficiency due to recurrent episodes of unilateral adrenal infarction
    
    ea0110ep150
  - Addison's disease initially interpreted as sarcoidosis
    
    ea0110ep151
  - Elevated serum dehydroepiandrosterone sulfate in a young male without visible adrenal tumor
    
    ea0110ep152
  - When hormonal and oncologic pathologies collide: navigating management complexities of primary hyperaldosteronism with an incidental finding of renal cell carcinoma
    
    ea0110ep153
  - Bilateral gynecomastia revealing adrenocorticaloma
    
    ea0110ep154
  - Plasma steroid profiling in early diagnosis of adrenocortical carcinoma
    
    ea0110ep155
  - Non-neoplastic hypercortisolism state and adrenal incidentaloma: a clinical challenge?
    
    ea0110ep156
  - An incidental adrenal mass misleading to surgical intervention: a case of misleading imaging findings
    
    ea0110ep157
  - Adreanal hystopatology in primary aldosteronism: single centre expiriance
    
    ea0110ep158
  - A rare case of vanishing bilateral adrenal masses
    
    ea0110ep159
  - A case of sheehan syndrome presenting with acute coronary syndrome: a case report
    
    ea0110ep160
  - Cushing's disease in a patient presenting for oculomotor palsy-a diagnostic and management conundrum
    
    ea0110ep161
  - Ectopic secretion of ACTH: diagnosis and management a case report
    
    ea0110ep162
  - Late diagnosis of classic simple virilizing congenital adrenal hyperplasia in a young female
    
    ea0110ep163
  - Pheochromocytoma: case report
    
    ea0110ep164
  - COVID-19 and Addison's disease
    
    ea0110ep165
  - Revealing adrenal tumors as a primary cause of secondary high blood pressure
    
    ea0110ep166
  - Partial 21-hydroxylase deficiency in a 7-year-old: a rare cause of precocious puberty
    
    ea0110ep167
  - Vagal paraganglioma: a diagnostic surprise
    
    ea0110ep168
  - Hypertension secondary to primary hyperaldosteronism
    
    ea0110ep169
  - A lesson for life!
    
    ea0110ep170
  - Diagnosis and management of recurrent ipsilateral pheochromocytoma due to medium sized adrenal tumor with renal vascular invasion
    
    ea0110ep171
- Bone and Mineral Metabolism
- - Phosphate as the earliest marker of metabolic bone disease of prematurity
    
    ea0110ep172
  - Double trouble: when combination therapy does more harm than good
    
    ea0110ep173
  - Compromised muscle strength in patients with hypophosphatasia
    
    ea0110ep174
  - Adolescent body mass index and osteoporosis risk: a nationwide study of one million israeli adolescents
    
    ea0110ep175
  - Mineral-bone disorder in chronic kidney diseases as early atherosclerosis indicators
    
    ea0110ep176
  - Bridging osteoporosis and glucose metabolism: the insulin sensitivity benefits of denosumab
    
    ea0110ep177
  - Diagnostic accuracy of choline pet in primary hyperparathyroidism with negative localization studies: a preliminary analysis
    
    ea0110ep178
  - Juvenile primary hyperparathyroidism revealed by genu valgum
    
    ea0110ep179
  - Boxed in: should the black box warning for osteosarcoma be retired for good?
    
    ea0110ep180
  - Risk factors for osteoporosis in children with hyperthyroidism under iodine-deficient conditions in the Republic of Uzbekistan
    
    ea0110ep181
  - Autosomal dominant hypocalcemia type 1 (ADH1): management during pregnancy
    
    ea0110ep182
  - Do patients with ehlers-danlos syndrome and a history of fractures have lower bone mineral density?
    
    ea0110ep183
  - Duchenne muscular dystrophy and risk of fracture
    
    ea0110ep184
  - Osteogenesis imperfecta: a novel mutation in the COL1A1 gene and 8 new patients in Greece
    
    ea0110ep185
  - Clinical and molecular profiles of 14 new patients with X-linked hypophosphatemia (XLH) in greece
    
    ea0110ep186
  - Bone metabolism in refractory rickets: a comparative study of treatment-compliant, non-compliant, and healthy children
    
    ea0110ep187
  - Relationship between vitamin D deficiency and low bone mineral density in children with inflammatory bowel diseases
    
    ea0110ep188
  - Novel association between cohen syndrome and low alkaline phosphatase, a potential new subgroup of hypophosphatasia
    
    ea0110ep189
  - A rare cause of short stature: the journey to diagnosing hypophosphatemic rickets with hypercalciuria
    
    ea0110ep190
  - Successful treatment of autosomal dominant hypophosphatemic rickets with burosumab: a case report
    
    ea0110ep191
  - Buschke-ollendorff syndrome in a mother-child duo: a rare cause of short stature and skeletal dysplasia
    
    ea0110ep192
  - At the crossroads: femoral osteonecrosis in [beta]-thalassemia major
    
    ea0110ep193
  - Treatment conundrums in newly recognized early-onset osteoporosis caused by heterozygous WNT1 mutation
    
    ea0110ep194
  - Hypercalcemia in primary hyperparathyoidism: when should ENT be alerted?
    
    ea0110ep195
  - Cartilage -hair hypoplasia due to double heterozygosity for the RMRPn.97_98dup mutation and the RMRPn.25_-12dup mutation in a girl with asymmetrical short stature and brachydactyly
    
    ea0110ep196
  - Effect of sacubitri/valsartan on bone turnover markers in patients with dilated cardiomyopathy
    
    ea0110ep197
  - Clinical, biochemical and radiological features of LRP5 gene variants in children: case series and literature review
    
    ea0110ep198
  - Bone turnover markers and their associations with longitudinal changes in bone mineral density and trabecular bone score in children and adolescents with graves' disease
    
    ea0110ep199
  - Palopegteriparatide for the treatment of autosomal dominant hypocalcemia type 1 (ADH1)
    
    ea0110ep200
  - Vitamin d replenishment and its effectiveness on bone health in children receiving antiepileptic drugs: a randomized controlled trial
    
    ea0110ep201
  - The achondroplasia roadmap
    
    ea0110ep202
  - A rare case of genetically confirmed X-linked dominant hypophosphatemic rickets in a 7-year-old girl from Kazakhstan
    
    ea0110ep204
  - Tumor-induced osteomalacia: the bone metabolism version of the princess and the pea
    
    ea0110ep205
  - Premature girl with unusual skeletal dysplasia
    
    ea0110ep206
  - Isolated mild hypocalcemia as the initial manifestation of previously undiagnosed Coeliac disease
    
    ea0110ep207
  - New clues that may connect the circulating irisin levels to glucose status and bone turnover markers in postmenopausal women (project IRI-OP-OB)
    
    ea0110ep208
  - Evaluation of a new IDS beta crosslaps® (CTX-I) assay for the iSYS automated analyzer
    
    ea0110ep209
  - Evaluation of children with persistently low ALP levels
    
    ea0110ep210
  - A rare cause of hypoparathyroidism: kenny caffey type 2 - case report
    
    ea0110ep211
  - The role of surgery in tertiary hyperparathyroidism with ectopic localization
    
    ea0110ep212
  - Do patients with ehlers-danlos syndrome and a history of fractures have calcium and phosphate metabolism disturbances?
    
    ea0110ep213
  - Not just another adenoma: the diagnostic challenges of atypical parathyroid lesions
    
    ea0110ep214
  - Bone and mineral metabolism alterations in newly diagnosed hyperthyroid patients
    
    ea0110ep215
  - Parathyroid cysts: about 10 cases
    
    ea0110ep216
  - A complex case of developmental anomalies, endocrinopathies, and neurological symptoms: albright hereditary osteodystrophy (AHO)
    
    ea0110ep217
  - Growth failure and chondrodysplasia following early hematopoietic stem cell transplantation for familial lymphohistiocytosis: a case report
    
    ea0110ep218
  - Case report and follow-up of juvenile paget's disease caused by TNFRSF11B mutations in sibling pair
    
    ea0110ep219
  - Evaluation of the Impact of Therapeutic Patient Education (TPE) on Quality of Life Compared to Standard Care and Injectable Parathyroid Hormone Treatment in Chronic Hypoparathyroidism
    
    ea0110ep220
  - Osteopenic males PHPT patients: prevalence and clinical features
    
    ea0110ep221
  - Prevention of rebound hypercalcemia in giant cell bone lesions treated with denosumab: a critical comparison of two different approaches
    
    ea0110ep222
  - Bone-specific alkaline phosphatase as a complementary diagnostic marker for the assessment of children and adolescents with secondary osteoporosis
    
    ea0110ep223
  - Novel allelic variants in Sanjad-Sakati and Kenny-Caffey syndromes identified by whole exome sequencing
    
    ea0110ep224
  - Iatrogenic hypoparathyroidism revealed by amicrobial pustulosis following total thyroidectomy: a case report
    
    ea0110ep225
  - Hypoparathyroidism: clinical and genetic characteristics with long-term outcomes
    
    ea0110ep226
  - Cinacalcet in primary hyperparathyroidism: QEHB audit
    
    ea0110ep227
  - Intravenous Bisphosphonates for Severe Hypercalcemia in Primary Hyperparathyroidism: Do We Need to Draw an Analogy From Osteoporosis Experience?
    
    ea0110ep228
  - Bone mineral density alterations in primary hyperparathyroidism: clinical and diagnostic implications
    
    ea0110ep229
  - Perspectives of patients and families on X-linked hypophosphatemic rickets (XLH) and its impact on quality of life: a qualitative study
    
    ea0110ep230
  - An exceptionally cause of fahr's syndrome: pseudohypoparathyroidism
    
    ea0110ep231
  - Severe hypocalcemia and psoriasis: an intriging link
    
    ea0110ep232
  - The potential (secondary) use of a calcilytic drug to prevent postoperative hypoparathyroidism
    
    ea0110ep233
  - Genetic skeletal disorders: phenotypic-genotypic characteristics and rhgh therapy responses of a pediatric cohort from a single center in china
    
    ea0110ep234
  - Analysis of the therapeutic effect of burosumab in the treatment of 6 children with x-linked hypophosphatemia
    
    ea0110ep235
  - utility of parathyroid index and calcium to phosphorous ratio in diagnosis of normocalcemic primary hyperparathyroidsm
    
    ea0110ep236
  - Effect of bisphosphonates on parathyroid adenoma in patients undergoing focused parathyroidectomy for primary hyperparathyroidism with hypercalcemic crisis
    
    ea0110ep237
  - Body fat mass influences hip geometry in adult male diabetic patients: A community-based study from North India
    
    ea0110ep238
  - Familial hypocalciuric hypercalcemia due to a novel CASR mutation: diagnostic challenges and clinical implications
    
    ea0110ep239
  - Severe hypercalcemia with persistent nausea and vomiting in a child with new-onset graves' disease
    
    ea0110ep240
  - Pseudohypoparathyroidism type 1c - a rare cause of obesity in children- a case report
    
    ea0110ep241
  - Pseudohypoparathyroidism type 1B and thyroid hemiagenesis: a case report
    
    ea0110ep242
  - A case of resistant hypocalemia and hungry bone syndrome after parathyroidectomy
    
    ea0110ep243
  - Fahr's syndrome with hypoparathyroidism: a case report
    
    ea0110ep244
  - Evaluation of cinacalcet prescribing and monitoring in primary hyperparathyroidism: a single-centre audit
    
    ea0110ep245
  - Experience of using cinacalcet for the treatment of secondary hyperparathyroidism in uzbekistan
    
    ea0110ep246
  - Novel VDR gene mutation in a vitamin D-dependent rickets type 2A compound heterozygote:a case report
    
    ea0110ep247
  - Evaluation of the effect of hypercortisolemia treatment on bone metabolism and structure in patients with endogenous cushing's syndrome- a single center experience
    
    ea0110ep248
  - PTH-independent hypercalcemia in a young adult due to a compound heterozygous CYP24A1 mutation
    
    ea0110ep249
  - An adolescent with spondyloepiphyseal dysplasia congenita and nephrocalcinosis: value of genetic testing in understanding complex clinical presentations
    
    ea0110ep250
  - The outcome of parathyroidectomy for secondary hyperparathyroidism in hemodilaysis patients
    
    ea0110ep251
  - Pseudohypoparathyroidism revealed by bone pain: a case report
    
    ea0110ep252
  - A rare parathyroid lipoadenoma in a patient with sporadic multiglandular primary hyperparathyroidism - pitfalls in preoperative localization and pathological diagnosis
    
    ea0110ep253
  - A young case of hyperparathyroidism-jaw tumor syndrome carrying a large deletion of the CDC73 gene
    
    ea0110ep254
  - Is burosumab a good choice?: experience in adult X-linked hypophosphatemic rickets in a turkish patient
    
    ea0110ep255
  - A curious case of trips and falls: pseudohypoparathyroidism
    
    ea0110ep256
  - Hypercalcaemia with unsuppressed parathyroid hormone level: a diagnostic dilemma; a case series
    
    ea0110ep257
  - The management of X-linked hypophosphatemia: oral phosphate and calcitriol supplementation vs. burosumab. a case report
    
    ea0110ep258
  - Family hypomagnesemia and hypercalciuric nephrocalcinosis: a case report and literature review
    
    ea0110ep259
  - Association between bone turnover markers, bone mineral density, and serum osteoglycin in middle-aged men with Type 2 Diabetes mellitus
    
    ea0110ep260
  - Clot twist: deep vein thrombosis uncovers primary hyperparathyroidism
    
    ea0110ep261
  - Primary hyperparathyroidism and monoclonal gammopathy of undetermined significance: a misleading association? A case report
    
    ea0110ep262
  - Autoimmune polyglandular syndrome type 2: when calcium steps in
    
    ea0110ep263
  - Alfacalcidol shortage in morocco and its impact on patient care: a retrospective study
    
    ea0110ep264
  - Secondary hyperparathyroidism in patients with chronic renal failure
    
    ea0110ep265
  - Suspected growth hormone deficiency as a mask of hypophosphatasia in a male patient with verified compound heterozygous variant in ALPL gene
    
    ea0110ep267
  - Case of successful management of primary hyperparathyroidism and incidentally found micro PTC during pregnancy
    
    ea0110ep268
  - About a rare association: primary hyperparathyroidism and clear cell renal cell carcinoma
    
    ea0110ep269
  - A young male patient presented with hypercalcemia due to familial hypocalceuric hypercalcemia type 1
    
    ea0110ep270
  - Rare case of concomitant pseudohypoparathyroidism and bilateral ovarian teratoma
    
    ea0110ep271
  - Acute hypercalcemia after immune checkpoint inhibitor therapy with pembrolizumab. A case report
    
    ea0110ep272
  - Hyperphosphatemic familial tumoral calcinosis in an omani child: case report
    
    ea0110ep273
  - Persistent hyperparathyroidism and bilateral oncocytic adrenocortical carcinoma: interplay of endocrine and oncologic challenges
    
    ea0110ep274
  - PROPEL: prospective observational registry for ENPP1 deficiency and early-onset ABCC6 deficiency
    
    ea0110ep275
  - Grading pseudofractures—the [ldquo]breach - beak - bump - bridge[rdquo] approach
    
    ea0110ep276
  - Radiofrequency ablation in primary hyperparathyroidism: a case study and literature review
    
    ea0110ep277
  - Hypocalciuric hypercalcemia: navigating the diagnostic challenges
    
    ea0110ep278
  - Rocky road to diagnosis: uncovering primary hyperparathyroidism
    
    ea0110ep279
  - Pregnancy and lactation-associated osteoporosis with multiple spinal fragility fractures
    
    ea0110ep280
  - Ectopic parathyroid adenoma associated with a thymoma: a case report
    
    ea0110ep281
  - Assessment of bone mineral density and it's determinants in children with precocious puberty
    
    ea0110ep282
  - Cystic angiomatosis. a diagnostic challenge - case report
    
    ea0110ep283
  - A rare case of primary hyperparathyroidism caused by a giant parathyroid adenoma: a case report
    
    ea0110ep284
  - Renaltu, a web page to satisfy the information needs on primary tubulopathies for patients and care provider
    
    ea0110ep285
  - Profound hyponatremia in acute heart failure with a good outcome
    
    ea0110ep286
  - Design of 3 multicenter, phase 3, randomized trials to evaluate efficacy and safety of the enzyme replacement therapy efzimfotase alfa in patients with hypophosphatasia (HICKORY, MULBERRY, CHESTNUT)
    
    ea0110ep287
  - Interest of the bone scintigraphy in the diagnosis and monitoring of enchondroma, about a case
    
    ea0110ep288
  - Mass effect revealing a sphenoidal brown tumor: a case report
    
    ea0110ep289
  - Familial hyperparathyroidism due to gcm² gene alteration: a case report
    
    ea0110ep290
  - Geriatric patient presenting with severe hypercalcemia due to suspicious parathyroid carcinoma
    
    ea0110ep291
  - A case of primary hyperparathyroidism due to an oxyphil cell adenoma
    
    ea0110ep292
  - Imaging in X-linked hypophosphataemia (XLH)
    
    ea0110ep293
  - Primary hyperparathyroidism: from diagnosis to treatment
    
    ea0110ep294
  - Demystifying an unusual culprit and analyzing implications for management: a case of lithium-induced parathyroid hyperplasia presenting as severe symptomatic hypercalcemia
    
    ea0110ep295
  - Two different causes of hypercalcemia
    
    ea0110ep296
  - Osteoporosis at a young age: an issue for endocrinologists - a case report
    
    ea0110ep297
  - Adrenal glands, pancreas, and urinary catheter calcifications in a 59-year-old woman with primary hyperparathyroidism
    
    ea0110ep298
  - An intrathyroidal parathyroid adenoma: a location not to be ignored!
    
    ea0110ep299
  - Palopegteriparatide use for severe postoperative hypocalcemia
    
    ea0110ep300
  - Dermatological disorders associated with hypocalcaemia: a case report
    
    ea0110ep301
  - A falsely labeled primary hyperparathyroidism: about a case report
    
    ea0110ep302
  - Primary hyperparathyroidism meets fibromyalgia: a crossroads of symptoms
    
    ea0110ep303
  - ENT manifestations of the relapsing polychondritis (RP) in diabetic patients
    
    ea0110ep304
  - The phantom hormone: decoding bone loss in a breast cancer patient
    
    ea0110ep305
  - Pseudohypoparathyroidism 1b diagnosed in middle adulthood with an atypical presentation: a case report
    
    ea0110ep306
  - Hypercalcemia as the initial manifestation of sarcoidosis: a case series
    
    ea0110ep307
  - A case report: COL1A1 mutation with albright hereditary osteodystrophy (AHO) features
    
    ea0110ep308
  - Waddling gait and parathyroid adenoma: what to have in mind for a quick diagnosis?
    
    ea0110ep309
  - Extremely rare association of primary hyperparathyroidism and familial hypocalciuric hypercalcemia
    
    ea0110ep310
  - Sjogren's syndrome revealing familial hypocalciuric hypercalcemia: a case report
    
    ea0110ep311
  - Osteoporotic fractures in hypogonadotropic hypogonadism linked to PROKR2 gene mutation
    
    ea0110ep312
  - Pitfalls and challenges in the management of secondary hyperparathyroidism and mineral and bone disorders associated with CKD
    
    ea0110ep313
  - Giant parathyroid adenoma revealed by severe hypercalcemia and disabling bone pain: case report
    
    ea0110ep314
  - Method for increasing the ultrasonic conductivity of skull bone tissue in patients who are planned to be treated with magnetic resonance imaging-guided focused ultrasonic imaging
    
    ea0110ep315
- Diabetes and Insulin
- - Blood sugar profiles in children receiving high doses of systemic glucocorticoids
    
    ea0110ep316
  - The role of muscular fitness on bone mineral content and areal bone mineral density in children and adolescents with type 1 diabetes: a 2-year longitudinal analysis of the diactive-1 cohort study
    
    ea0110ep317
  - Impact of emergency admission on glycemic control in hospitalized diabetic patients
    
    ea0110ep318
  - Screening for prenatal depression in women with gestational diabetes: the relationship with self-esteem and social support
    
    ea0110ep319
  - Identification of cardiometabolic phenotypes and key indicators in patients with arterial hypertension, type 2 diabetes mellitus, and obesity
    
    ea0110ep320
  - Correlation of hypoglycemic episodes and cognitive functions in people with diabetes mellitus
    
    ea0110ep321
  - The evaluation of arterial stiffness indices in children and adolescents with type 1 diabetes mellitus or excess weight
    
    ea0110ep322
  - Profile of chronic diabetes complications in hospitalized patients: A multicenter tunisian study
    
    ea0110ep323
  - Impact of surgical interventions on glycemic control in hospitalized diabetic patients
    
    ea0110ep324
  - The transition from pediatric to adult care in type 1 diabetes: A real challenge
    
    ea0110ep325
  - Association of AGES and obstructive sleep apnea in patients with diabetes
    
    ea0110ep326
  - Uncovering underlying causes: a crucial step in managing diabetic ketoacidosis
    
    ea0110ep327
  - Relationship between polymorphic markers rs7903146 variant of TCF7L2 gene, rs10830963 variant of mtnr1b gene and rs1801282 variant of pparg (pro12ala) gene and various subtypes of gestational diabetes mellitus
    
    ea0110ep328
  - Effect of vitamin D supplementation on metabolic and psychopathological disorders in patients with type 2 diabetes mellitus in chronic stress conditions
    
    ea0110ep329
  - Prevalence of sarcopenia and dinapenia in young population with type 1 diabetes mellitus
    
    ea0110ep330
  - Relationship between severe hypoglycemia and time in range in type 1 and type 2 diabetes patients
    
    ea0110ep331
  - Impact of corticosteroid therapy on glycemic control in hospitalized diabetic patients
    
    ea0110ep332
  - What fears do women with gestational diabetes face?
    
    ea0110ep333
  - Spontaneous pneumomediastinum: a rare complication of diabetic ketoacidosis
    
    ea0110ep335
  - A case of HAIRAN syndrome in a teenage girl with hirsutism and secondary amenorrhea
    
    ea0110ep336
  - PAX4 mody - a novel variant
    
    ea0110ep337
  - Sodium-glucose cotransporter 2 inhibitors in type 1 diabetes mellitus: prohibited?
    
    ea0110ep338
  - Efficacy on functionality and perceived quality of life of a nutritional support programme with specific supplementation for people with type 2 diabetes at risk of malnutrition
    
    ea0110ep339
  - Vitamin D and glycemic control in type 1 diabetes
    
    ea0110ep340
  - Fighting with a double-edged sword: a case of pancreatic transplant failure with resurgence of autoimmune diabetes in a patient with metastatic colon cancer treated with pembrolizumab
    
    ea0110ep341
  - When karyotype is necessary in hyperinsulinemic hypoglycemia:a case report in mosaic turner syndrome
    
    ea0110ep342
  - Incidence and survival implications of diabetic nephropathy in post-heart transplant patients
    
    ea0110ep343
  - Prediabetes and systemic inflammation
    
    ea0110ep344
  - Hypogonadism - is it more frequent in males with type 1 diabetes mellitus?
    
    ea0110ep345
  - Fear of hypoglycemia: a significant challenge for pregnant women with type 1 diabetes
    
    ea0110ep346
  - Dysglycemias in HNF1-b-associated disease: phenotype-genotype correlations
    
    ea0110ep347
  - Study of the clinical profile of diabetics followed up in front-line structures
    
    ea0110ep348
  - Retrospective evaluation of clinical and metabolic differences in the course of diabetic ketoacidos in patients with diabetes mellitus using SGLT-2 inhibitors: a single center study
    
    ea0110ep349
  - Trends in diabetic foot infections in albania: a decade of insights into etiology and risk factors
    
    ea0110ep350
  - The importance of interleukin 6 in the detection of silent myocardial ischemia in patients with tipe 2 diabetes
    
    ea0110ep351
  - Multifocal sporadic insulinoma with both intra- and peri-pancreatic lesions: a rare case report
    
    ea0110ep352
  - Increased utilization of diabetes technology and improved glycaemic control among children with type 1 diabetes in Hong Kong over the past 8 years
    
    ea0110ep353
  - Early diagnosis of acromegaly in patient with with type 1 diabetes based on glycemic data measured using an advanced hybrid closed loop system
    
    ea0110ep354
  - A 3-year follow-up of a diabetes-nephrology outpatient service for managing patients with type 2 diabetes and chronic kidney disease
    
    ea0110ep355
  - Evaluation of clinical, laboratory and immunological characteristics in the early onset (diagnosed age
    
    ea0110ep356
  - New technologies counteracting genetic errors: a case report
    
    ea0110ep358
  - Blood sugar peaks and valleys: visualizing glucose patterns through world´s highest mountains
    
    ea0110ep359
  - p deletion syndrome associated with type 1 diabetes and hashimoto's thyroiditis: a case report on autoimmune disorders and genetic factors
    
    ea0110ep360
  - Two rare monogenic diabetes cases due to CEL mutations: one with MODY 8 phenotype, one presenting as type 1 diabetes
    
    ea0110ep361
  - Frequency of cardiovascular autonomic neuropathy and its association with microvascular complications in states of glucose tolerance abnormalities
    
    ea0110ep362
  - Type 2 diabetes was linked to asthma: a meta-analysis
    
    ea0110ep363
  - Treatment of hyperuricemia as an option for slowing the progression of diabetic nephropathy
    
    ea0110ep364
  - Main epidemiological indicators of diabetes mellitus among the urban population on the example of Minsk (2014-2024)
    
    ea0110ep365
  - The transition phase and glycemic control: insights from 100 patients study
    
    ea0110ep366
  - Glycemic control in type 1 diabetes patients transitioning from pediatric to adult care
    
    ea0110ep367
  - Early-onset diabetic neuropathy in a teenager with brittle type 1 diabetes: a case report
    
    ea0110ep368
  - Ultrasound monitoring for chemotherapy complications in diabetic patients
    
    ea0110ep369
  - A rare case of MODY12 (ABCC8 Mutation) presenting with both congenital hyperinsulinism and maturity onset diabetes of the young
    
    ea0110ep370
  - From group to individual: how paediatric diabetes education is changing in the era of technology
    
    ea0110ep371
  - Donohue syndrome: three case studies illustrating clinical heterogeneity and management challenges
    
    ea0110ep372
  - Impact of smoking and physical activity on cardiovascular outcomes in type 2 diabetes with metabolic dysfunction-associated steatotic liver disease: a nationwide study
    
    ea0110ep373
  - Yellowish appearance - an unusual presentation of type 1 diabetes mellitus in children
    
    ea0110ep374
  - Neonatal diabetes mellitus in a boy with wolfram-like syndrome
    
    ea0110ep375
  - Type 1 diabetes, SARS-CoV-2 and vitamin D3
    
    ea0110ep376
  - Technological implementation and evolution of metabolic control in pediatric T1D patients: [ldquo]real life experience[rdquo]
    
    ea0110ep377
  - Lada diabetes in older patients: clinical diagnostic implications of imaging and laboratory biomarkers
    
    ea0110ep378
  - Evaluating the reach of hellotype1: a digital innovative educational platform in regional languages for diabetes education in southeast asia
    
    ea0110ep379
  - Association of metformin use and vitamin b intake with dementia risk in non-diabetic people: insights from the UK biobank
    
    ea0110ep380
  - In the heat of the moment: burns uncover the silent diabetes
    
    ea0110ep381
  - Prevalence and clinical impact of obesity in patients living with type 1 diabetes
    
    ea0110ep382
  - Effect of subcutaneous semaglutide in patients with type 2 diabetes mellitus on the degree of systemic inflammation
    
    ea0110ep383
  - Effect of subcutaneous semaglutide on liver fibrosis degree in patients with type 2 diabetes mellitus measured by the FIB-4 index
    
    ea0110ep384
  - Biological changes in new-onset diabetic ketoacidosis (DKA) before and during covid-19
    
    ea0110ep385
  - Study on insulin gene rs689 polymorphism in patients with diabetic neuropathy
    
    ea0110ep386
  - Treatment of 1182 early type I DM with a combination of 3 immune modulatory drugs Eight years of experience
    
    ea0110ep387
  - Superimposition of increased beta oxidation due to insulin deficiency is the principal molecular mechanism of diabetic ketoacidosis: a proportional hazard model
    
    ea0110ep388
  - Association between body composition parameters, disease duration, and glycemic control in adult patients with type 1 diabetes: a cross-sectional study
    
    ea0110ep389
  - Demographic and clinical characteristics of patients with LADA diabetes at hospital universitario de canarias, spain
    
    ea0110ep390
  - Characteristics of patients with diabetes mellitus evaluated by hospital interconsultations at the canarias university hospital (HUC)
    
    ea0110ep391
  - A diagnosis of MODY 2 following MIS-C
    
    ea0110ep392
  - Melatonin levels across patients with type 2 diabetes mellitus with and without sleep disorders
    
    ea0110ep393
  - Fibrocalculous pancreatic diabetes (SPINK 1 mutation) in klinefelter syndrome: first case report
    
    ea0110ep394
  - Localized scleroderma in a type 1 diabetic patient: a case report
    
    ea0110ep395
  - Predictors of diabetes in tropical calcific pancreatitis - a cross sectional, observational study
    
    ea0110ep396
  - The importance of cardiovascular implementation tests in diagnostic of the diabetic cardiovascular autonomic neuropathy
    
    ea0110ep397
  - Prevalence of obesity and diabetes in reproductive age (20-44 years) in the bulgarian population
    
    ea0110ep398
  - New-onset autoimmune diabetes mellitus concomitantly with myositis secondary to pembrolizumab treatment in a patient with squamous lung cancer: a case report
    
    ea0110ep399
  - Type 2 diabetes and quality of life in relation to perceived psychological stress
    
    ea0110ep400
  - Hypoglycemia in an insulin-treated diabetic: when causes pile up
    
    ea0110ep401
  - Evolution of glycemic profile of diabetic women after childbirth
    
    ea0110ep402
  - A case of insulin antibody-mediated insulin resistance in type 2 diabetes treated by glucocorticoid
    
    ea0110ep403
  - Diabetes as a major risk factor for pharyngostoma: influence of comorbidities on postoperative outcomes
    
    ea0110ep404
  - An unusual cause of hypoglycemia: insulin autoimmune syndrome
    
    ea0110ep405
  - On the evaluation of the significance of hyperuricemia from the position of belonging to the metabolic syndrome
    
    ea0110ep406
  - Diabetes mellitus in acute exacerbation of chronic obstructive pulmonary disease. retrospective study
    
    ea0110ep407
  - Post-surgical biliary pancreatitis and GAD positive diabetes: a rare case of type 3c DM with autoimmune features
    
    ea0110ep408
  - Working time and metabolic syndrome- analysis of indian data
    
    ea0110ep409
  - Durability of glycemic response with FDC of sitagliptin and metformin in treatment naive T2DM indian patients from a real-world retrospective EMR based study
    
    ea0110ep410
  - Hybrid closed loop in a residential setting: it takes a village but it is worth it
    
    ea0110ep411
  - Role of pre-pregnancy weight and weight gain during pregnancy on maternal and fetal outcomes: real word data from an italian centre
    
    ea0110ep412
  - Nephroprotective treatment with dapagliflozin in patients with diabetic kidney disease
    
    ea0110ep413
  - Predictive factors for the use of insulin therapy in gestational diabetes
    
    ea0110ep414
  - The use of hybrid closed-loop systems in a pediatric population with type 1 diabetes mellitus- a real-world retrospective study
    
    ea0110ep415
  - Congenital hyperinsulinism: same parents, different genetics. regarding two cases
    
    ea0110ep416
  - Role of dedicated DSN: improving outcomes through intervention and support
    
    ea0110ep417
  - Two cases of wolfram syndrome in bulgarian children from pleven region
    
    ea0110ep418
  - A favorable factors influencing glycemic control in pediatric type 1 diabetes patients
    
    ea0110ep419
  - Trends and outcomes in pediatric diabetes management after universal coverage expansion: a single tertiary care experience in Thailand
    
    ea0110ep420
  - Parotid lithiasis revealing previously undiagnosed diabetes mellitus: a case report
    
    ea0110ep421
  - Diabetes associated with childhood lipodystrophies: clinical characteristics and management
    
    ea0110ep422
  - Mody: when to consider? when should genetic tests be performed?
    
    ea0110ep423
  - A very rare case of MODY 12: inactivating ABCC8 mutation causing sulfonylurea-resistant diabetes
    
    ea0110ep424
  - Single center study on evaluating and mitigating key factors associated with extended hospitalisation in patients admitted for hypoglycaemia
    
    ea0110ep425
  - Case series of patients with euglycemic diabetic ketoacidosis
    
    ea0110ep426
  - Determination of antioxidant activity in seminal plasma of diabetic and non-diabetic individuals
    
    ea0110ep427
  - Severe acute pancreatitis secondary to major hypertriglyceridemia associated with diabetic ketoacidosis
    
    ea0110ep428
  - Allergic reaction following the injection of human insulin
    
    ea0110ep429
  - Clinical management and outcomes of diabetic foot ulcers: a study of 322 cases
    
    ea0110ep430
  - Diagnosis and therapeutic management of infected diabetic foot: insights from 278 cases
    
    ea0110ep431
  - Impact of glycemic profile on severe hypoglycemia recurrence in diabetic patients
    
    ea0110ep432
  - Use of automated insulin delivery systems in pregnant women with type 1 diabetes: real-world data
    
    ea0110ep433
  - Influence of socioeconomic factors on breastfeeding adherence in a group of diabetic women
    
    ea0110ep434
  - Epidemiology of type 1 diabetes in children: a 5-year study
    
    ea0110ep435
  - Diabetic ketoacidosis (DK) in the context of COVID-19: epidemiological and clinical insights
    
    ea0110ep436
  - Hyperuricemia: is it a cardiovascular risk factor?
    
    ea0110ep437
  - Generalized lipodystrophy masquerading as obesity and insulin resistance
    
    ea0110ep438
  - Measurement of insulin secretion during oral glucose tolerance test for prediction of obesity treatment success
    
    ea0110ep439
  - Screening for celiac disease in children with type 1 diabetes, is it necessary? twenty-five years of experience in a single center
    
    ea0110ep440
  - Development of disease-modifying therapies for early-stage type 1 diabetes: insights from the EDENT1FI project
    
    ea0110ep441
  - HbA1c measurement: comparison of biorad D10 (Hplc) and sebia capillarys 2 methods
    
    ea0110ep442
  - Factors associated with gestational weight gain in pregnant women with gestational diabetes mellitus
    
    ea0110ep443
  - Diabetic foot in patients with type 1 diabetes: a challenging complication (a study of 56 patients)
    
    ea0110ep444
  - Impact of glycemic imbalance on diabetic foot ulcer healing
    
    ea0110ep445
  - Microbiological spectrum of diabetic foot infections (a study of 46 cases)
    
    ea0110ep446
  - Lipid profile and micro and macrovascular complications in LADA diabetes at hospital universitario de canarias, spain
    
    ea0110ep447
  - Correlation between visceral fat, insulinresistance and age in type 1 diabetes patients
    
    ea0110ep448
  - Association between diabetes mellitus and severity of epistaxis: a retrospective study
    
    ea0110ep449
  - Electroconvulsive therapy and the onset of diabetes: a rare but critical complication in children
    
    ea0110ep450
  - Atezolizumab-induced autoimmune diabetes mellitus: clinical case
    
    ea0110ep451
  - Use of diabetes app to help improve management of adolescent type 1 dm patients
    
    ea0110ep452
  - Parenting style and glycemic control in adolescents with type 1
    
    ea0110ep453
  - Higher prevalence of mental health impairment in youth with diabetes and association of higher HbA1c with physical complaints
    
    ea0110ep454
  - Beyond blood sugar: body composition changes in children with T1DM
    
    ea0110ep455
  - Unilateral ptosis in a patient with graves' disease and multiple sclerosis: a diagnostic challenge
    
    ea0110ep457
  - Microbiota profiling in diabetic foot infections at oran university hospital: a study from the endocrinology-diabetology department
    
    ea0110ep458
  - Beliefs and eating habits in pregnant diabetic women
    
    ea0110ep459
  - Gestational diabetes: clinical profile, screening methods, and management approach
    
    ea0110ep460
  - Educational factors and their impact on metabolic management in diabetic patients
    
    ea0110ep461
  - Do we consider cardiovascular risk in patients with type 1 diabetes mellitus? a cross-sectional observational study at the canary islands university hospital complex (CHUC)
    
    ea0110ep462
  - Diabetic retinopathy in hospitalized patients: a multicenter tunisian study
    
    ea0110ep463
  - An atypical presentation of malignant otitis externa in a diabetic patient
    
    ea0110ep464
  - Kaposi sarcoma manifesting as leg lesions in a patient with diabetes mellitus: a case report
    
    ea0110ep465
  - Co-occurrence of Ketoacidosis Decompensation and Acute Pancreatitis in Type 1 Diabetic Patients: Clinical and Biological Specificities
    
    ea0110ep466
  - Asymptomatic hyperuricemia: prevalence and risks
    
    ea0110ep467
  - Association of type 1 diabetes and celiac disease
    
    ea0110ep468
  - A complex case of Type 1 DM with history of recurrent severe disabling hypoglycaemia treated with renal and pancreatic transplant
    
    ea0110ep469
  - Refocusing on the implications for management: a case of hyporeninemic hypoaldosteronism in a patient with diabetic nephropathy presenting with severe hyperkalemia
    
    ea0110ep470
  - Newly diagnosed LADA in elderly people: a case study
    
    ea0110ep471
  - Epidemiological, clinical, and therapeutic profiles of pre-existing diabetes in pregnancy: exploring complications in a moroccan cohort
    
    ea0110ep472
  - Clinical profile of patients with nondiabetic hypoglycemia in a tertiary endocrine center in Nepal
    
    ea0110ep473
  - Planned postpartum screening study for cardiometabolic and renal outcomes in women diagnosed with gestational diabetes mellitus in Auckland, new Zealand
    
    ea0110ep474
  - Time in tight range (TITR) stratified by coefficient of variation (CV) in a cohort of patients with type 1 diabetes mellitus and multiple daily injections. a real-life study
    
    ea0110ep475
  - Characteristics of diabetic ketoacidosis episodes treated at HUC between 2021 and 2023
    
    ea0110ep476
  - Association between diabetes mellitus and severity of epistaxis: a retrospective study
    
    ea0110ep477
  - The role of chronic diabetic imbalance in increasing the risk of hepatic fibrosis
    
    ea0110ep478
  - Metabolic profile of tunisian type 2 diabetes patients at insulin initiation: a retrospective study
    
    ea0110ep479
  - A rare presentation of type 1 diabetes mellitus: cornelia de lange syndrome presenting with nonketotic hyperosmolar state
    
    ea0110ep480
  - Ketotic decompensation revealing early-stage fournier gangrene complicating type 2 diabetes
    
    ea0110ep481
  - Diabetes mellitus in equatorial guinea: community-based primary health care intervention
    
    ea0110ep482
  - Charming circle between iron and vitamin D deficiencies in women with type 2 diabetes mellitus and heart failure with preserved ejection fraction
    
    ea0110ep483
  - Gestational diabetes: about an algerian population
    
    ea0110ep484
  - Potential of dietary polyphenols in prevention and treatment of type 2 diabetes and different types of dementia
    
    ea0110ep485
  - Marked inflammatory syndrome revealing type 1 autoimmune hepatitis in a young female patient with type 2 diabetes
    
    ea0110ep486
  - Prevalence of lipohypertrophy and associated factors among insulin-treated diabetes mellitus patients
    
    ea0110ep487
  - Unusual case of pancreatic neoplasm revealed by insulin initiation in a diabetic patient
    
    ea0110ep488
  - Comparative characteristics of carbohydrate metabolism in patients with different types of autoimmune diabetes
    
    ea0110ep489
  - Prevalence of autoimmune disorders in pediatric and adolescent patients with type 1 diabetes mellitus: a retrospective cohort study
    
    ea0110ep490
  - Severe ketoacidosis and multi-organ failure in a type 2 diabetes mellitus patient: a case report
    
    ea0110ep491
  - "Sweet testosterone" - improved metabolic compensation after starting testosterone therapy in two transgender adolescents
    
    ea0110ep492
  - Alpha-lipoic acid-induced insulin autoimmune syndrome: an emerging public health risk
    
    ea0110ep493
  - Polymorphisms of leptin`s gene in different types of diabetes mellitus
    
    ea0110ep494
  - Steroid-induced diabetes: when ocular treatment becomes a metabolic threat
    
    ea0110ep495
  - Dietary impact on the onset of MASLD in patients living with type 2 diabetes
    
    ea0110ep496
  - Association between neutrophil-to-lymphocyte ratio and metabolic syndrome in diabetic patients: a cross-sectional study
    
    ea0110ep497
  - Study on sialic acid concentrations in type 1 and type 2 diabetes mellitus
    
    ea0110ep498
  - Bilateral femoral head necrosis in early adulthood with pituitary stalk interruption syndrome: need for comprehensive medical education on the impact of growth retardation in misdiagnosis
    
    ea0110ep499
  - Prevalence of sarcopenia in indians with type 1 diabetes mellitus
    
    ea0110ep500
  - HbA1c measurement: comparison of biorad D10 (Hplc) and sebia capillarys 2 methods
    
    ea0110ep501
  - Factors impacting glycemic balance in pregnant diabetic women
    
    ea0110ep502
  - Euglycemic diabetic ketoacidosis in a type 1 diabetic: a case without SGLT2 inhibitors
    
    ea0110ep503
  - Type 1 diabetes in patients over 50: clinical and biological characteristics
    
    ea0110ep504
  - The complexity of diabetes management in MELAS syndrome: a personalized approach to glycaemic control
    
    ea0110ep505
  - Psychosocial experience of gestational diabetes in a population of tunisian women
    
    ea0110ep506
  - Blood lipid profile of patients with diabetes mellitus of various degrees of severity
    
    ea0110ep507
  - Growth assessment during puberty in children and adolescents with type 1 diabetes mellitus
    
    ea0110ep508
  - Type 2 diabetes mellitus in teenagers - a growing concern for armenia
    
    ea0110ep509
  - It is not always insulinoma
    
    ea0110ep510
  - Successful treatment of a foot ulcer in a female patient with newly diagnosed T1DM (LADA)
    
    ea0110ep511
  - Diabetic foot ulcer. peripheral artery disease and treatment with angioplasty
    
    ea0110ep512
  - Exploring the role of type 2 diabetes mellitus factors in the progression to advanced fibrosis in MASLD
    
    ea0110ep513
  - Perceived stress levels in women with gestational diabetes and associated factors
    
    ea0110ep514
  - Mauriac syndrome and autoimmune hepatitis: a rare combination in a patient with type 1 diabetes
    
    ea0110ep515
  - Vitamin D and microvascular complications in type 1 diabetes
    
    ea0110ep516
  - Specificities by gender of macroangiopathic complications in type 2 diabetic patients
    
    ea0110ep517
  - Gender differences in prevalence, clinical features, and treatment of hypertension in type 2 diabetes
    
    ea0110ep518
  - Unconventional use of continuous glucose monitoring: case report
    
    ea0110ep519
  - Vitamin D status and features of carbohydrate metabolism in fertile women with diabetes mellitus
    
    ea0110ep520
  - Elevated risk of life-threatening metabolic acidosis with combined metformin and SGLT2 inhibitor therapy in the elderly
    
    ea0110ep521
  - Hepatic glycogenosis in poorly controlled type 1 diabetes mellitus
    
    ea0110ep522
  - Challenge in the follow-up of a type 1 diabetic patient with short stature - how craniopharyngioma can disturb the hormone status
    
    ea0110ep523
  - Genetic diagnosis of MODY: a case highlighting the role of 17q12 deletion
    
    ea0110ep524
  - Severe hypercalcemia in a teenager with inaugural diabetic ketoacidosis
    
    ea0110ep525
  - Quality of life in patients with diabetes mellitus
    
    ea0110ep526
  - Unveiling the cardio-metabolic factors driving advanced fibrosis in type 2 diabetic patients with MASLD
    
    ea0110ep527
  - Prevalence of metabolic dysfunction-associated steatotic liver disease in patients with type 2 diabetes mellitus: a tunisian study
    
    ea0110ep528
  - Dietary impact on the risk of progression to hepatic fibrosis in patients with type 2 diabetes
    
    ea0110ep529
  - Influence of degenerative complications of diabetes on the occurrence of infections
    
    ea0110ep530
  - Cardiovascular risk in relation to Body Mass Index in patients with type 2 diabetes mellitus
    
    ea0110ep531
  - Can we predict the onset or worsening of microangiopathies in pregnant women with diabetes mellitus during pregnancy?
    
    ea0110ep532
  - Case of complete remission of diabetes mellitus type 1
    
    ea0110ep533
  - Diabetic ketoacidosis secondary to immunotherapy-induced diabetes mellitus
    
    ea0110ep534
  - Impact of gestational diabetes and maternal obesity on fetal growth: reduced length and cephalic circumference
    
    ea0110ep535
  - Solving a hypoglycaemia mystery
    
    ea0110ep536
  - Mucormycosis infections in a child with type 1 diabetes mellitus
    
    ea0110ep537
  - Renal complications in diabetic subjects
    
    ea0110ep538
  - Effects of weight loss after bariatric surgery on pregnancy outcome
    
    ea0110ep539
  - Kyrle's disease: a rare complication of diabetes (case report)
    
    ea0110ep540
  - Stress perception among patients with type 1 diabetes
    
    ea0110ep541
  - Tracing the causes: why hypoglycemia strikes in type 1 diabetes mellitus
    
    ea0110ep542
  - Antidiabetic treatment patterns in type 2 diabetic patients with metabolic associated steatotic liver disease
    
    ea0110ep543
  - Type 2 diabetes-related features in patients with metabolic associated steatotic liver disease
    
    ea0110ep544
  - Chronic kidney disease in type 2 diabetes patients with metabolic associated steatotic liver disease
    
    ea0110ep545
  - Mycosis fungoides and diabetes mellitus: is there a link?
    
    ea0110ep546
  - Diabetic retinopathy in normoalbuminuric patients with type 2 diabetes mellitus: any predictive factors?
    
    ea0110ep547
  - Vitamin D status in type 1 diabetic tunisian patients: a case-control study
    
    ea0110ep548
  - Acute pancreatitis in type 1 diabetic patients: etiological and evolutionary profile
    
    ea0110ep549
  - Microbiota and type 2 diabetes: current status and future perspectives
    
    ea0110ep550
  - Assessment of nutritional status in elderly diabetics in hospital
    
    ea0110ep551
  - Type 2 diabetes diagnosed after 10 years of insulin therapy
    
    ea0110ep552
  - Impact of vitamin d and vitamin d receptor activator in diabetic nephropathy
    
    ea0110ep553
  - Targeted, rapid glycaemic control and its potential adverse outcomes
    
    ea0110ep554
  - Unbalanced diabetes leads to orbital myositis with oculomotor nerve palsy (ONP)
    
    ea0110ep555
  - Barriers to achieving glycemic control in type 2 diabetes mellitus: focus on therapeutic adherence
    
    ea0110ep556
  - Peri-esophageal infections due to foreign body in the esophagus: a serious complication in diabetic patients
    
    ea0110ep557
  - Benefits of SGLT2 inhibitors on cardiovascular and renal health in clinical practice
    
    ea0110ep558
  - Cardiometabolic profile in type 2 diabetics with vitamin D deficiency
    
    ea0110ep559
  - Hypoglycemia and autoimmune diabetes; a cause not to be
    
    ea0110ep560
  - Pancreatic diabetes: diagnostic, therapeutic, and evolutionary particularities
    
    ea0110ep561
  - Successful treatment of 138000 patients with multimodal drug approach
    
    ea0110ep562
  - Diabetes and self-harm: a struggle beyond the surface
    
    ea0110ep563
- Endocrine Related Cancer
- - Incidence and survival of neuroendocrine neoplasia in the maltese islands - a population-based study
    
    ea0110ep564
  - V804M RET mutation screening and familial medullary thyroid carcinoma in the Maltese Islands
    
    ea0110ep565
  - Usefulness of the braf gene study in the evaluation of the thyroid nodule
    
    ea0110ep566
  - Diffuse large B-cell lymphoma leading to polyendocrine involvement (pituitary, adrenal, and thyroid)
    
    ea0110ep567
  - Bone metastases revealing a follicular carcinoma of the thyroid
    
    ea0110ep568
  - Autoimmune endocrinopathies associated with the use of immune checkpoint inhibitors: a clinical case of a combination of primary hypothyroidism due to destructive thyroiditis and diabetes mellitus
    
    ea0110ep569
  - Hyperprolactinemia and cancer risk: a swedish population-based cohort study
    
    ea0110ep570
  - Cowden syndrome: a case report
    
    ea0110ep571
  - Neuroendocrine tumors in association with other primary neoplasms
    
    ea0110ep572
  - Case series: ¹³¹I-MIBG treatment in pheochromocytoma and paraganglioma - insights from our experience
    
    ea0110ep573
  - A case of a 5.5-years-old girl with clitoromegaly, cafe-au-lait spots and a pathogenic variant in NF1 gene inherited from the mother
    
    ea0110ep574
  - A unique case of pheochromocytoma crisis leading to hypoxic cardiac arrest requiring veno-arterial-venous extracorporeal membrane oxygenation (ECMO) in a postpartum patient
    
    ea0110ep575
  - Higher incidence of fatigue in thyroid cancer survivors transitioning to primary care compared to other cancer survivors
    
    ea0110ep576
  - Impact of adjuvant mitotane on long-term outcomes in patients at high risk of adrenocortical carcinoma recurrence
    
    ea0110ep577
  - Pubertal arrest, polydipsia, polyuria, headaches and diplopia in a 13 year old girl
    
    ea0110ep578
  - Bilateral and malignant reninoma - case presentation
    
    ea0110ep579
  - Delayed diagnosis of an optic chiasm germinoma in a child: clinical evolution and metabolic consequences
    
    ea0110ep580
  - Gastroenteropancreatic neuroendocrine tumours (GEP-NETs): clinical profile, treatment and 10-year survival
    
    ea0110ep581
  - A rare case of chronic diarrhoea: medullary carcinoma of the thyroid
    
    ea0110ep582
  - A unique case of both adrenal and extra-adrenal paragangliomas in a patient with parkinson's disease
    
    ea0110ep583
  - Pediatric papillary thyroid carcinoma
    
    ea0110ep584
  - Gastric microbiota and antioxidants in patients with autoimmune atrophic gastritis and gastric neuroendocrine tumors
    
    ea0110ep585
  - Papillary thyroid carcinoma: a case of pulmonary metastasis
    
    ea0110ep586
  - Oestradiol: immunoassay measurement can be inaccurate in patients taking fulvestrant
    
    ea0110ep587
  - SPECT/CT skeletal muscle cancer in bronchial cancer, about a case
    
    ea0110ep588
  - Epidemiologic profile of differentiated thyroid cancer in algeria
    
    ea0110ep589
  - Uncommon thyroid cancer concurrence: a case of papillary microcarcinoma and medullary thyroid carcinoma
    
    ea0110ep590
  - Pituitary Adenoma as the First Manifestation of MEN1: A Case Report
    
    ea0110ep591
  - ENT monitoring following radioactive iodine (RAI) therapy in patients treated for papillary thyroid carcinoma
    
    ea0110ep592
  - An unusual first manifestation of pheochromocytoma leading to the discovery of a MEN2A family
    
    ea0110ep593
  - The hidden danger of small thyroid nodules: unmasking hereditary medullary thyroid carcinoma
    
    ea0110ep594
  - Ectopic cushing's syndrome associated with poorly differentiated nasal squamous cell carcinoma
    
    ea0110ep595
  - Differentiated high-grade thyroid carcinoma in pregnancy
    
    ea0110ep596
  - Radiolabeled somatostatin receptor antagonist in patients with metastatic pheochromocytoma or paraganglioma; dosimetry, efficacy and safety evaluation
    
    ea0110ep597
  - Challenging management of paraneoplastic cushing's syndrome: a 13 year clinical journey
    
    ea0110ep598
  - A rare source of ectopic ACTH secretion causing cyclical cushing's syndrome
    
    ea0110ep599
  - Niosome-encapsulated quercetin for enhanced thyroid cancer therapy and potential minimization of thyroid surgery
    
    ea0110ep600
  - Challenges in treatment of carotid paraganglioma: about a case report
    
    ea0110ep601
  - Toddler-age girl with rapidly progressing peripheral precocious puberty
    
    ea0110ep602
  - Adrenocortical carcinoma with co-secretion of aldosterone and cortisol: a case report
    
    ea0110ep603
  - When two cancers collide: a case of rectal adenocarcinoma following thyroid cancer
    
    ea0110ep604
  - Reabilitation of patients who was operate from the thyroid cancer
    
    ea0110ep605
  - Follicular thyroid carcinomas: epidemiological, clinical, and therapeutic profiles
    
    ea0110ep606
  - 177Lu-edotreotide versus everolimus in patients with advanced neuroendocrine tumors of lung or thymic origin: progress of the LEVEL / GETNE-t2217 trial
    
    ea0110ep608
  - Family matters! - a rare case of SDHB gene linked metastatic paraganglioma
    
    ea0110ep609
  - Molecular and functional characterisation of the somatostatin system unravels novel vulnerabilities in hepatocellular carcinoma
    
    ea0110ep610
  - A case of long-standing pituitary macroadenoma leading to panhypopituitarism and visual impairment
    
    ea0110ep611
  - A case of severe hyponatremia due to SIAD likely caused by uterine sarcoma
    
    ea0110ep612
  - Primary adrenal insufficiency secondary to bilateral adrenal metastasis of a prostatic adenocarcinoma: a case report
    
    ea0110ep613
  - When secondary localizations reveal papillary thyroid carcinoma: a case report
    
    ea0110ep614
  - Gastrinoma and zollinger ellison syndrome: a management roadmap
    
    ea0110ep615
  - Anatomopathological characteristics of papillary thyroid carcinomas associated with autoimmune thyroid disease
    
    ea0110ep616
  - Effective treatment of metastatic insulinoma in MEN-1 syndrom with pasireotide
    
    ea0110ep617
  - Late endocrine disorders in surviving children with acute lymphoblastic leukemia: single center study in Egypt
    
    ea0110ep619
  - Unveiling hidden hyperparathyroidism: the critical role of calcium and PTH measurement in early diagnosis
    
    ea0110ep620
  - The impact of metabolic syndrome on survival outcomes in urothelial carcinoma: a retrospective cohort study
    
    ea0110ep621
  - Asymptomatic insulinoma diagnosed following a motor vehicle accident: a case report
    
    ea0110ep622
  - A lung cancer patient presenting with gynecomastia and mastodynia secondary to paraneoplastic hyperestrogenism
    
    ea0110ep623
  - Humeral metastasis of papillary thyroid carcinoma: a rare localisation in a case report
    
    ea0110ep624
  - Phenotypic diversity in patients carrying the Y791F RET proto-oncogene mutation
    
    ea0110ep625
  - Association of schmidt syndrome with papillary thyroid carcinoma
    
    ea0110ep626
  - Parathyroid carcinoma on secondary hyperpara-thyroidism: a case report
    
    ea0110ep627
  - Primary hyperparathyroidism and papillary carcinoma of the thyroid: about a case
    
    ea0110ep628
  - Primary thyroid lymphoma: About 2 cases
    
    ea0110ep629
  - Hypercalcemia as a first manifestation of metastatic neuroendocrine tumour
    
    ea0110ep630
  - Endocrine status on glucose, thyroid and calcium metabolism after treatment for breast cancer in postmenopausal women
    
    ea0110ep631
  - Treatment of a catecholamine-secreting vagal paraganglioma with fractionated stereotactic radiotherapy
    
    ea0110ep632
  - Unexpected evolution of an ACTH secreting pitnet
    
    ea0110ep633
  - Calcium as a tumour marker in PTHrP-secreting pancreatic neuroendocrine tumour: a case of multimodal management
    
    ea0110ep634
  - Hypoglycemia secondary to metastatic solitary fibrous tumor: doege-potter syndrome. importance of the IGF-II/IGF-I ratio
    
    ea0110ep635
  - An unusual evolution of a malignant metastatic pheochromocytoma: A case report
    
    ea0110ep636
  - Thyroid metastasis of pulmonary choriocarcinoma: a rare and challenging diagnosis
    
    ea0110ep637
  - A rare combination of three endocrine neoplasms and cervical adenocarcinoma
    
    ea0110ep638
  - Successful management of papillary thyroid microcarcinoma with distant metastases: a case report
    
    ea0110ep639
  - Medullary thyroid cancer and infiltrating ductal carcinoma of the breast: a rare association
    
    ea0110ep640
  - Papillary thyroid carcinoma associated with primary hyperparathyroidism: a rare occurrence
    
    ea0110ep641
  - A case of ectopic ACTH secretion caused by thymic neuroendocrine tumor (typical carcinoid) with metastasis to the breast after long-term remission
    
    ea0110ep642
  - Cervical lymph nodes metastasis revealing occult papillary thyroid carcinoma
    
    ea0110ep643
  - An unusual case of cervical mass.a case report
    
    ea0110ep644
  - Incidental detection of papillary thyroid carcinoma on 18F-FDG PET/CT: a case report
    
    ea0110ep645
  - Unusual skeletal muscle metastasis from poorly differentiated thyroid carcinoma: a rare presentation
    
    ea0110ep646
  - Adrenocortical carcinoma: a deadly challenge
    
    ea0110ep647
  - The hidden complexity of adrenal tumors: six cases that challenge diagnosis and treatment
    
    ea0110ep648
  - Parathyroid carcinoma synchronous with multifocal papillary thyroid microcarcinoma presenting as recurrent retropharyngeal hematoma in 45 years old woman
    
    ea0110ep649
  - Effects of osilodrostat and metyrapone on 2D and 3D models of adrenocortical carcinoma cell lines viability: preliminary results
    
    ea0110ep650
  - Two unusual calcitonin negative medullary thyroid carcinomas
    
    ea0110ep651
  - Lymph node metastasis revealing a thyroid microcarcinoma in a patient monitored for laryngeal cancer
    
    ea0110ep652
  - Unexpected presentation of pancreatic metastasis in B-cell Lymphoma
    
    ea0110ep653
  - A rare case report of prolonged adrenal insufficiency following discontinuation of osilodrostat treatment for severe hypercortisolism due to ectopic ACTH syndrome
    
    ea0110ep654
  - Persistent virilization in a woman with CAH under medical treatment: a hidden culprit
    
    ea0110ep655
  - Peroperatory isotopic detection and mini invasive surgery, what prospects?
    
    ea0110ep656
  - Bilateral gynecomastia unveiling an adrenal cortical tumor
    
    ea0110ep657
  - A diagnostic dilemma: revisiting the utility of selective arterial calcium stimulation testing for localization of occult insulinoma
    
    ea0110ep658
  - Sporadic medullary carcinoma: case report
    
    ea0110ep659
  - Unusual case of prolactinoma mimicking stroke
    
    ea0110ep660
  - Great response to mitotane in advanced adrenocortical carcinoma
    
    ea0110ep662
  - A bilateral vestibular schwannoma in neurofibromatosis type 2
    
    ea0110ep663
  - An atypical presentation of a patient with neuroendocrine tumor
    
    ea0110ep664
  - Risk factors and malnutrition in colorectal cancer patients: identification and clinical implications
    
    ea0110ep665
  - Lung neuroendocrine tumours: clinical aspects and methods of investigation
    
    ea0110ep666
- Environmental Endocrinology
- - Molecular docking analysis of endocrine disruptors at the androgen receptor's ligand-binding domain
    
    ea0110ep667
  - Exposure to endocrine disruptors in the NICU: the chemical footprint in premature newborns
    
    ea0110ep668
  - Tracking endocrine disruptor effects of chlorobenzenes in AVP and OT mediated processes in Wistar? rat models
    
    ea0110ep669
  - Perceptions and concerns about endocrine disruptors in the real-life of Italian family pediatricians: preliminary data of a national survey. (On behalf of ISPED Endocrine Disruptors Study Group)
    
    ea0110ep671
  - Survey of attitudes and knowledge about endocrine disruptors among the student population of the republic of Serbia
    
    ea0110ep672
  - Seep survey of knowledge on endocrine disruptors in pediatrics: disenped study
    
    ea0110ep673
  - Chronotypes of medical residents and their association with career choice
    
    ea0110ep674
  - Vitamin D deficiency during pregnancy in the presence of prenatal maternal stress and their association with the development of attention-deficit/hyperactivity disorder like symptoms in toddlers
    
    ea0110ep675
  - Impact of lyposomal PC5 on rats behavioral activity
    
    ea0110ep676
  - Big data tools for assessing the nutritional situation of a pediatric population: did the prevalence of obesity change pre- and post-pandemic?
    
    ea0110ep677
  - Teplizumab for type 1 diabetes in children: a paradigm shift in treatment
    
    ea0110ep678
  - Clinical features of hypercalcemic crisis due to primary hyperparathyroidism
    
    ea0110ep679
  - Parental perception and knowledge of childhood obesity: descriptive study in tunisia
    
    ea0110ep680
  - Patient preference for gender of treating endocrinologist
    
    ea0110ep681
  - Primary hyperparathyroidism and pancreatitis: a rare and multifaceted association
    
    ea0110ep682
  - Primary hyperparathyroidism due to ectopic parathyroid lesions: our experience
    
    ea0110ep683
  - Gender differences in specialty choices among medical residents
    
    ea0110ep684
  - The night shift: impacts of delayed sleep patterns on endocrine function, growth, and puberty in adolescents
    
    ea0110ep685
  - Living on the edge: war, stress, and autoimmune diabetes
    
    ea0110ep686
  - Possible effects of the COVID-19 pandemic on the prevalence of malnutrition-anorexia cases in a pediatric population. using BIG DATA tools
    
    ea0110ep687
  - Thyroid health in the age of night shifts: the role of circadian disruption
    
    ea0110ep688
  - Endocrine disruptions in the kabuki syndrome spectrum
    
    ea0110ep689
  - Detection cases of childhood malnutrition using BIG DATA techniques: social and economic determinants
    
    ea0110ep690
- Fetal and Neonatal Endocrinology
- - Feeding issues: an under-recognized complication in people with hyperinsulinism
    
    ea0110ep691
  - Influence of maternal dietary protein precursor on reproductive endocrinology of neonatal bovine offspring
    
    ea0110ep692
  - Calculation of risk factors in medical vs. surgical treatment for persistent hyperinsulinemic hypoglycemia of infancy: a systematic review of long-term outcomes"
    
    ea0110ep693
  - Neonatal vitamin D deficiency as a risk factor for the development of bronchopulmonary dysplasia: a systematic review and meta-analysis
    
    ea0110ep694
  - Association of early nutrition and growth and metabolic parameters in very low birth weight infants
    
    ea0110ep695
  - Genetic characteristics and clinical management of patients with diazoxid-unresponsive congenital hyperinsulinism in Slovakia
    
    ea0110ep696
  - Serum neudesin levels in patients with congenital hypothyroidism
    
    ea0110ep697
  - Evaluation of clinical characteristics of syndromic and non-syndromic monogenic diabetes presented at neonatal and childhood period in a highly consanguineous population
    
    ea0110ep698
  - Managing daily challenges in congenital hyperinsulinism: impacts and solutions for improved quality of life"
    
    ea0110ep699
  - Neonatal hypocalcemic seizures revealing asymptomatic maternal hyperparathyroidism: case report and literature revue
    
    ea0110ep700
  - Novel mutation in TBX1 in a neonate with hypocalcemic seizures and digeorge syndrome
    
    ea0110ep701
  - Necrolytic migratory erythema following prolonged continuous subcutaneous Dasiglucagon administration: a case report
    
    ea0110ep702
  - Evaluation of a new guideline for the early detection and management of neonatal hypoglycaemia
    
    ea0110ep703
  - Cloudy blood, clear diagnosis: homozygous GP1HBP1 mutation in a 20 day old neonate
    
    ea0110ep704
  - Unraveling genotype-phenotype interactions in congenital hyperinsulinemic hypoglycemia: implications for targeted therapies and diazoxide responsiveness
    
    ea0110ep705
  - "Genotype and phenotype-driven probability of therapeutic response in congenital hyperinsulinism"
    
    ea0110ep706
  - The role of surgery in the 3rd trimester in the management of hypercalcaemia in pregnancy
    
    ea0110ep707
  - Clinical experience with various persistent congenital hyperinsulinisms in a single tertiary care center: a case series
    
    ea0110ep708
  - Comparative outcomes of medical and surgical management in children with persistent neonatal hyperinsulinemic hypoglycemia: a focus on long-term growth, metabolic, and developmental implications"
    
    ea0110ep709
  - Hypoglycemia screening before discharge in newborn identified as at risk
    
    ea0110ep710
  - New insights into hypothalamic dysfunction: schaaf-yang syndrome in two infants
    
    ea0110ep711
  - A case of PURA syndrome characterized mainly by hypotonia and hypersomnia
    
    ea0110ep712
  - Cardiometabolic function in offspring, mother and placenta after assisted reproductive technology (COMPART)
    
    ea0110ep713
  - Update on the association of prenatal and postnatal exposures to acetaminophen and neurodevelopmental disorders
    
    ea0110ep714
  - The neonatal TSH screening as an indicator of the iodine status in newborns in bulgaria: actual data 2021-2024
    
    ea0110ep715
  - A rare case of a male infant in mini-puberty presenting with premature pubarche and non-classical congenital adrenal hyperplasia
    
    ea0110ep716
  - A macrosomic preterm baby with hypoinsulinemic hypoketotic hypoglycemia: a diagnostic puzzle
    
    ea0110ep717
- Growth Axis and Syndromes
- - The effects of long-acting pegylated recombinant human growth hormone (jintrolong) on body composition and bone mass in transitional growth hormone deficiency
    
    ea0110ep719
  - Overgrowth: one patient, two syndromes
    
    ea0110ep720
  - Clinical and genetic characteristics of cornelia de lange syndrome: a retrospective study of 20 pediatric patients in China
    
    ea0110ep721
  - Development of AI-based growth prediction models for children with growth disorders: a 3-year analysis using the lg growth study
    
    ea0110ep722
  - The molar ratio of IGF-1/IGFBP-3 serves as a biomarker for evaluating the therapeutic efficacy of recombinant human growth hormone
    
    ea0110ep723
  - Celiac disease and short stature: sometimes it is not just gluten
    
    ea0110ep724
  - Rare case of DPH1 syndrome: report of a patient with two novel variants
    
    ea0110ep725
  - Osteogenesis imperfecta/ehler danlos overlap syndrome
    
    ea0110ep726
  - Growth hormone testing in prader willi syndrome: our experience with glucagon test
    
    ea0110ep727
  - Disease activity drop-off in elderly patients with active acromegaly over a median follow-up period of ten years: a longitudinal, restrospective study
    
    ea0110ep728
  - Clinical heterogeneity of sanjad sakati syndrome: experience from a single tertiary center in kuwait
    
    ea0110ep729
  - Short stature in CHARGE syndrome
    
    ea0110ep730
  - q26.3 Deletion effect on growth: a case report
    
    ea0110ep731
  - Is L-dopa test effective in detecting adrenal insufficiency with preliminary diagnosis of growth hormone deficiency in children with short stature?
    
    ea0110ep732
  - Treatment responce of the growth hormone in 3M syndrome: a single center experience
    
    ea0110ep733
  - "A shared GHSR gene variant in children with short stature and growth hormone deficiency: potential clinical relevance"
    
    ea0110ep734
  - Development of a minimum dataset (MDS) for the monitoring of growth hormone therapy in children with prader willi syndrome (PWS) - a globe-reg initiative
    
    ea0110ep735
  - Three decades of growth hormone therapy in prader-willi syndrome: insights from belgium
    
    ea0110ep736
  - New evidence of growth hormone treatment benefit on bone mineralization during transition from paediatric to adult care in a growth hormone deficient french cohort
    
    ea0110ep737
  - Insulin tolerance test for the diagnosis of adult GH deficiency: definition of BMI-dependent cut-offs using a clinical gold standard
    
    ea0110ep738
  - GLP-1 receptor agonists as therapeutic approach to severe obesity in PHP/iPPSD: two case reports
    
    ea0110ep739
  - The effects of long-acting growth hormone therapy on serum GH and IGF-i levels and potential safety risks compared to physiological pulsatile growth hormone and daily gh injections
    
    ea0110ep740
  - Positive impact of healthcare professionals' interaction with a digital health platform on patient adherence to recombinant human growth hormone therapy
    
    ea0110ep741
  - Results of treatment with recombinant human growth hormone (rhGH) in patients with noonan syndrome. albanian experience
    
    ea0110ep742
  - Growh patterns and genotype-phenotype correlations in tricho-rhino-phalangeal syndrome type i: insights from a korean cohort
    
    ea0110ep743
  - Noonan syndrome: a retrospective observational study from a paediatric endocrinology unit at a portuguese tertiary hospital
    
    ea0110ep744
  - An atypical case of silver-russel syndrome linked to a novel variant in HMGA2 gene
    
    ea0110ep745
  - A single center real world experience with vosoritide for the treatment of children with achondroplasia
    
    ea0110ep746
  - Sex steroid priming prior to growth hormone stimulation testing in peripubertal adolescents with short stature?
    
    ea0110ep747
  - Lamb-Shaffer syndrome as a rare cause of short stature
    
    ea0110ep748
  - Identification of a novel heterozygous variant of the aggrecan gene in a family with idiopathic short stature and accelerated bone maturation: treatments and challenges
    
    ea0110ep749
  - Differences in age at treatment start of recombinant human growth hormone therapy among european countries
    
    ea0110ep750
  - (Un)satisfactory effectiveness of whole-exome sequencing in detecting genetic causes of differential sexual development in 46,XY patients
    
    ea0110ep751
  - Mixed segmental uniparental disomy of chromosome 15q11-q1 coexists with homozygous variant in GNB5 gene in child with Prader-Willi and Lodder-Merla syndrome
    
    ea0110ep752
  - The impact of growth hormone treatment on physical performance in adult patients with severe growth hormone deficiency - preliminary results
    
    ea0110ep753
  - Severe growth hormone deficiency in siblings: a case study of GH1-related IGHD in a consanguineous family
    
    ea0110ep754
  - Integrating patient-generated health data into growth hormone therapy: perspectives from the paediatric endocrinologists in the gulf cooperation council
    
    ea0110ep755
  - Self-resolving regional lipodystrophy secondary to somatrogon therapy: a case report
    
    ea0110ep756
  - Filippi syndrome - a rare syndrome as a cause of short stature and primary amenorrhea
    
    ea0110ep757
  - Survey of electronic growth chart use reveals inconsistent provision and awareness of functionality across the United Kingdom
    
    ea0110ep758
  - Real world data for the first year of treatment with somatrogon of children and adolescents with growth hormone deficiency (GHD)
    
    ea0110ep759
  - Growth hormone treatment response in patients with biologically inactive growth hormone
    
    ea0110ep760
  - Intellectual and developmental function in children with Silver-Russell syndrome
    
    ea0110ep761
  - Patient dynamics and real-world insights from a somatropin patient support program (PSP): outcomes from 24,000 treated patients in brazil
    
    ea0110ep762
  - Adherence and its key-driving factors to growth hormone treatment in children with growth disorders: the french SCOPE study
    
    ea0110ep763
  - Paradoxical growth in multiple pituitary deficiencies: two clinical cases of obese pediatric patients
    
    ea0110ep764
  - Growth hormone insensitivity in an infant with LZTR1 mutation and growth failure: a case report
    
    ea0110ep765
  - Autosomal recessive ovarian dysgenesis associated to gh-deficiency and pituitary hyperplasia: a case report
    
    ea0110ep766
  - Experience with vosoritide for achondroplasia: insights from Kazakhstan
    
    ea0110ep767
  - Optimizing therapies for advanced bone age in obesity-related short stature, cah, precocious puberty, and sga: an updated view
    
    ea0110ep768
  - A rare cause of short stature: a case with a TBX6 gene variant
    
    ea0110ep769
  - A rare disease presented with bow legs
    
    ea0110ep770
  - A case of spondyloepiphyseal dysplasia, kimberley type, caused by a novel variant in the ACAN gene
    
    ea0110ep771
  - Evaluation of factors that predict a good response to growth hormone treatment in patients with isolated growth hormone deficiency in first year of therapy - single centre study
    
    ea0110ep772
  - Mauriac syndrome in a teenager with dual autoimmune disorders: a case report
    
    ea0110ep773
  - Effects of growth hormone therapy in patients with prader-willi syndrome: the first algerian experience
    
    ea0110ep774
  - The rare co-occurence of pituitary gigantism and thrombocytopenia!
    
    ea0110ep775
  - Response to recombinant growth hormone therapy in an indian girl with 3-M syndrome
    
    ea0110ep776
  - A paediatric case of progeroid lipodystrophy due to a de novo mutation in POLD1 gene
    
    ea0110ep777
  - Case series on growth hormone deficiency: clinical and endocrinological insights
    
    ea0110ep778
  - SEENEZ trial: growth prediction model from mid-puberty to near-adult height in adolescents with idiopathic isolated growth hormone deficiency treated with growth hormone
    
    ea0110ep779
  - Short stature in short bowel syndrome: complex interplay between nutrition and growth
    
    ea0110ep780
  - Comorbidities in pediatric turner syndrome: differences between 45,X0 and mosaic karyotypes
    
    ea0110ep781
  - Insights from IGF-1 generation test responses in growth disorders
    
    ea0110ep782
  - Growth and pubertal outcomes in CHARGE syndrome: a case study of hormone replacement therapy
    
    ea0110ep783
  - Our experience with somatrogon: therapeutic efficacy, adult height, safety and adherence
    
    ea0110ep784
  - A post market observational study to evaluate user's perception on technology acceptance and usability of two generations of digital devices to manage growth disorders across france and spain
    
    ea0110ep785
  - Neurofibromatosis type 1 revealed through growth delay: a case report
    
    ea0110ep786
  - Short stature due to ADAMTSL2 variant as a rare cause of geleophysic dysplasia: growth hormone had no role in treatment
    
    ea0110ep787
  - Access to growth hormone treatment for short stature children with noonan syndrome-the experience of the Wroclaw centre, poland
    
    ea0110ep788
  - Use of CGMS to identify early glucose changes in patients on growth hormone therapy
    
    ea0110ep789
  - Growth hormone therapy in montenegro over two decades
    
    ea0110ep790
  - An atypical case of a patient with prader-willi syndrome- difficult diagnostic pathway
    
    ea0110ep791
  - Bridging the treatment gap: growth hormone therapy for noonan syndrome in portugal
    
    ea0110ep792
  - Genotype-phenotype correlation of endocrine comorbidities in turner syndrome
    
    ea0110ep793
  - Role of molecular investigation for diagnosing short stature: a case report of a variant in the COL9A3 and UBA5 genes
    
    ea0110ep794
  - Growth hormone treatment in children with growth hormone deficiency: searching for predictors affecting adult height
    
    ea0110ep795
  - Enhancing paediatric care: insights from healthcare professionals on the quality and usability of digital devices in a participatory workshop in Korea
    
    ea0110ep796
  - Efficacy and safety of three-years growth hormone treatment in girls with turner syndrome and growth hormone deficiency: a case-control study
    
    ea0110ep797
  - Juberg-Marsidi syndrome coexisting with multihormonal hypopituitarism - a case report
    
    ea0110ep798
  - Circulating IGF-1 levels and trends in response to daily and weekly gh therapies: a comparative analysis
    
    ea0110ep799
  - Myhre syndrome - it is never too late
    
    ea0110ep800
  - Short stature and treatment in KBG syndrome: a case report
    
    ea0110ep801
  - Serum levels of intact and total IGFBP-4, and stanniocalcin-2 in congenital isolated gh deficiency
    
    ea0110ep802
  - The significance of cardiac MRI in transition care for Turner Syndrome: a prospective study
    
    ea0110ep803
  - Effects of gonadotropin-releasing hormone analog, alone and in combination with recombinant human growth hormone, on height in girls with early puberty across age groups
    
    ea0110ep804
  - ZTTK syndrome with growth hormone deficiency: a case report and literature review
    
    ea0110ep805
  - Whole exome sequencing uncovers the genetic diagnoses and new candidate genes for growth disorders in a cohort from the brazilian amazon
    
    ea0110ep806
  - Rare TXNRD2-related familial glucocorticoid deficiency in a chinese patient: a case report
    
    ea0110ep807
  - GH therapy and its short-term effectiveness in hong kong (the growth study)
    
    ea0110ep808
  - Identification of a novel IGF1R mutation in a family with short stature: a case report
    
    ea0110ep809
  - The impact of puberty on IGF-1: factors influencing growth and development
    
    ea0110ep810
  - Safety profile of large IGF-1 fluctuations: long-acting growth hormone therapy vs. daily growth hormone therapy
    
    ea0110ep811
  - Diagnostic utility of IGF-1 levels in growth and puberty-related disorders: a comprehensive review
    
    ea0110ep812
  - Are children with atopic eczema at higher risk of poor linear growth? - A systematic review of the literature
    
    ea0110ep813
  - Clinical features and genetic analysis of an SGA-born patient with IGF1R heterozygous mutation
    
    ea0110ep814
  - Experience with growth hormone therapy in a rare skeletal dysplasia
    
    ea0110ep815
  - Experience after 30 years of acromegaly management at the hospital clinico universitario de valladolid
    
    ea0110ep816
  - Cranio-lenticulo-sutural dysplasia (CLSD) as a rare cause of syndromic short stature: a case report of a complex clinical presentation
    
    ea0110ep817
  - Differences in treatment efficacy between idiopathic short stature and other conditions with advanced bone age
    
    ea0110ep818
  - INSIGHTS-GHT: first evaluation of paediatric patients with long-acting growth hormone therapy (LAGH) from the german registry
    
    ea0110ep819
  - Clinical and biochemical variation in a consanguineous family with heterozygous MAP2K2 variant and hetero/homozygous TSH receptor variant
    
    ea0110ep820
  - Prader-willi syndrome: a journey of resilience againt hyperphagia and developmental challenges
    
    ea0110ep821
  - Childhood growth hormone deficiency and continuation of therapy in adulthood: case series of patients followed at a tertiary center
    
    ea0110ep822
  - Noonan syndrome and growth delay: the hope of optimized growth with growth hormone therapy
    
    ea0110ep823
  - Skeletal ciliopathy and short rib dysplasia: a case report with response to growth hormone therapy
    
    ea0110ep824
  - A rare cause of short stature: cases with heterozygous mutations in the PCNT gene
    
    ea0110ep825
  - Beckwith wiedemann syndrome associated with transient typical features of classical congenital adrenal hyperplasia: a case report
    
    ea0110ep826
  - Differences in age, gender, and hormonal immunohistochemical profiles among patients with acromegaly and non-functioning pituitary adenomas
    
    ea0110ep827
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    ea0110ep828
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    ea0110ep829
  - Evaluating the IGF-1 generation test as a predictor of growth outcomes across pediatric growth disorders"
    
    ea0110ep830
  - A novel IGF1R variant in a patient with short stature in qatar
    
    ea0110ep831
  - Effect of urea ingestion on growth hormone levels in healthy adults - An analysis of a double-blind, randomized, placebo-controlled cross-over trial
    
    ea0110ep832
  - An early diagnosed leri-weill dyschondrosteosis case caused by unusual genetic results
    
    ea0110ep833
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    ea0110ep834
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    ea0110ep835
  - A clinical case of rasopathies caused by a mutation in the SHOC2 gene
    
    ea0110ep836
  - Pharmacological treatment of growth in boys with delayed or slow progression of puberty
    
    ea0110ep837
  - Spontaneous pregnancy in a patient with turner syndrome
    
    ea0110ep838
  - Shaff yang syndrome and growth hormone therapy
    
    ea0110ep839
  - Design of a randomized, multicentre, phase 2 study of vosoritide in children with turner syndrome, noonan syndrome, or short stature homeobox-containing gene (SHOX) deficiency
    
    ea0110ep840
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    ea0110ep841
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    ea0110ep842
  - Statural advance: a challenge for diagnosis and management
    
    ea0110ep843
  - Clinical and genetic analysis of three cases of short stature caused by the GHSR gene mutation in chinese
    
    ea0110ep844
  - Endocrine comorbidities in adult patients with Turner syndrome
    
    ea0110ep845
  - Somatotroph non functionnal pituitary adenoma: a case report
    
    ea0110ep846
  - A new prospective for the growth suppression in children with profound mental disability; case report and ethical consideration
    
    ea0110ep847
  - Glucose metabolism disorders in patients with acromegaly
    
    ea0110ep848
  - Pituitary acrogigantism from diagnosis to effective treatment- case study
    
    ea0110ep849
  - Two-year-old dizygotic twins diagnosed with rabson-mendenhall syndrome
    
    ea0110ep850
- Metabolism, Nutrition and Obesity
- - CiR-EIS sponges miR-548 to ameliorate metabolic dysfunction-associated steatohepatitis via regulating macrophage polarization
    
    ea0110ep851
  - Clinical and therapeutic characterization of patients with familial hypercholesterolemia: multicenter cross-sectional study
    
    ea0110ep852
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    ea0110ep853
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    ea0110ep854
  - Higher daytime systolic blood pressure, prepregnancy body mass index and an elevated sFlt-1/PlGF ratio predict the development of hypertension in normotensive pregnant women
    
    ea0110ep855
  - SGLT-2 inhibitors do not decrease tsh levels despite weight reduction, unlike GLP-1 agonists
    
    ea0110ep856
  - Gut microbiota and cytokine in children with nonalcoholic fatty liver disease
    
    ea0110ep857
  - Streamline - machine learning guided development of novel GLP-1 receptor agonists with improved drug properties
    
    ea0110ep858
  - High prevalence of MASLD already in children aged below 10 years
    
    ea0110ep859
  - Predictive factors of fat-free mass loss in obese patients after weight loss interventions
    
    ea0110ep860
  - A novel MED12 variant associated with early childhood-obesity
    
    ea0110ep861
  - Comparison of glucose-insulin-metabolism indices in obese male and female adolescents with equivalent height-normalised visceral and subcutaneous adipose tissue areas
    
    ea0110ep862
  - Metabolic syndrome and its components in overweight and obese children
    
    ea0110ep863
  - Effect of gliflozins on serum fetuin-a in patients with type 2 diabetes and nonalcoholic steatohepatitis
    
    ea0110ep864
  - Dapagliflozin protects against oxLDL-induced endothelial inflammation and oxidative damage by modulating the AMPK mechanism
    
    ea0110ep865
  - Challenges in the management of childhood obesity in primary care
    
    ea0110ep866
  - Phenotypic expression of biomolecular abnormalities in the leptin gene: a case report
    
    ea0110ep867
  - Evaluation of phenotypic age to improve screening and prognosis in patients with type 2 diabetes mellitus
    
    ea0110ep868
  - Changes in body composition among women users of anabolic androgenic steroids - suggestions of long-term impact on trunk fat accumulation
    
    ea0110ep869
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    ea0110ep870
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    ea0110ep871
  - Exploration of metabolic signatures or biomarkers associated with obesity in children and adolescents
    
    ea0110ep872
  - Comparative accuracy of glycemic parameters in identifying dysglycemia in obese indian children and adolescents
    
    ea0110ep873
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    ea0110ep874
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    ea0110ep875
  - Metabolic bariatric surgery reduces markers of aging in patients with obesity, independent of achieving optimal total weight loss
    
    ea0110ep876
  - Weight evolution in children of mothers with gestational diabetes: an analysis of the early years of life
    
    ea0110ep877
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    ea0110ep878
  - A rare syndrome hidden behind obesity
    
    ea0110ep879
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    ea0110ep880
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    ea0110ep881
  - Assessing allostatic load as a chronic stress marker in adolescents with anorexia nervosa: the impact of malnutrition
    
    ea0110ep882
  - Is gender affirming hormone therapy a risk factor for liver health? - 1-year follow-up data from a prospective study
    
    ea0110ep883
  - Gene diagnostic challenge of extreme early-onset obesity before 5 years old
    
    ea0110ep884
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    ea0110ep885
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    ea0110ep886
  - A rare case of hypertriglyceridaemia in infancy secondary to lipoprotein lipase deficiency
    
    ea0110ep887
  - Semaglutide treatment in hypotalamic obesity
    
    ea0110ep888
  - Clinical follow-up data of patients diagnosed with obesity
    
    ea0110ep889
  - Predicting models in patients with COVID-19 and metabolic syndrome
    
    ea0110ep890
  - Unraveling factors behind childhood obesity
    
    ea0110ep891
  - Assessment of nutritional status in obese adults undergoing weight loss interventions
    
    ea0110ep892
  - Phase angle as a predictor of nutritional status in middle-aged obese patients
    
    ea0110ep893
  - Does co-administration of lactate to an oral glucose tolerance test lower the glucose response - a randomized controlled cross-over study
    
    ea0110ep894
  - Genetic analysis of pediatric severe obesity in a single japanese instituition
    
    ea0110ep895
  - Comparison of metabolic disorders and obesity characteristics by household composition among korean adults: analysis of DINKs, married individuals with children, and unmarried individuals
    
    ea0110ep896
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    ea0110ep897
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    ea0110ep898
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    ea0110ep899
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    ea0110ep900
  - Ketogenic diet fails to counteract western diet-induced damage in skeletal muscle
    
    ea0110ep901
  - Body mass index and nutrition-related risk among older people
    
    ea0110ep902
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    ea0110ep903
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    ea0110ep904
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    ea0110ep905
  - A rare case of hutchinson-gilford progeria syndrome
    
    ea0110ep906
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    ea0110ep907
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    ea0110ep908
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    ea0110ep909
  - Obesity associated with macroprolactinoma: a case report
    
    ea0110ep910
  - Assessing body composition in individuals with obesity
    
    ea0110ep911
  - Baseline morphofunctional characteristics of a sample of transgender individuals from a specialized transgender healthcare unit
    
    ea0110ep912
  - Efficacy on nutritional status of a nutritional support programme with specific supplementation for people with type 2 diabetes at risk of malnutrition in routine clinical practice
    
    ea0110ep913
  - Evaluation of muscle strength in patients with type 1 diabetes mellitus: comparison of reference values
    
    ea0110ep914
  - Comparative analysis of morphofunctional parameters and clinical results in post-critical patients based on the definition of obesity used: body mass index or fat mass percentage
    
    ea0110ep915
  - Dietary factors contributing to overweight and obesity in children
    
    ea0110ep916
  - Nutrient intake in overweight patients with polycystic ovary syndrome (PCOS): a comparative study
    
    ea0110ep917
  - A study of interleukin-6 gene polymorphism in egyptian obese subjects
    
    ea0110ep918
  - Mitraa: transforming patient care through ai-driven chatbot technology
    
    ea0110ep919
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    ea0110ep920
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    ea0110ep921
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    ea0110ep922
  - Comprehensive insights into metformin: evidence from in vitro, cellular, animal, and human studies on obesity and cardiovascular health"
    
    ea0110ep923
  - Metformin in pediatric obesity: a safe and effective solution for lasting metabolic benefits
    
    ea0110ep924
  - Body composition and metabolic complications in a single-centre pilot cohort of adults with X-linked hypophosphatemia
    
    ea0110ep925
  - Long-term efficacy and safety of semaglutide in the treatment of syndromic obesity in prader willi syndrome - case series
    
    ea0110ep926
  - Abdominal adipose tissue ultrasound characterization in patients living with excess body fat: experience from our Centre
    
    ea0110ep927
  - Treatment of hypercholesterolemia with natural compounds
    
    ea0110ep928
  - F18 Choline PET-CT scan as single imaging modality for primary hyperparathyroidism
    
    ea0110ep929
  - Hyperglycemia in patients with acute myocardial infarction
    
    ea0110ep930
  - Metabolic changes and satisfaction associated with gender-affirming hormone therapy in transgender women
    
    ea0110ep931
  - Effect of a nutritional education program on anthropometric, biochemical, and body composition parameters in obese patients
    
    ea0110ep932
  - Morphofunctional changes during the follow up of people living with obesity treated with semaglutide
    
    ea0110ep933
  - Association between vitamin d levels at discharge, in-hospital complications and prevalence of obesity in post-critical care patients after admission to the icu for pneumonia covid-19
    
    ea0110ep934
  - Familial inheritance and childhood obesity
    
    ea0110ep935
  - Evaluation of the role of statins in the development of myalgias
    
    ea0110ep936
  - Pro-oxidant-antioxidant system in patients with chronic kidney disease and type 2 diabetes mellitus in obese and non-obese patients
    
    ea0110ep937
  - Biomarkers of iron status and inflammation in Belgian children with overweight and obesity
    
    ea0110ep938
  - Relationship between eating behavior of children with their nutritional status based on their bmi among 6 -12 year children: a mixed method study
    
    ea0110ep939
  - Premature aging in (young) adults with prader-willi syndrome
    
    ea0110ep940
  - The relationship between serum galectin-3 level and echocardiographic findings in patients with polycystic ovary syndrome
    
    ea0110ep941
  - Impact of obesity management during polycystic ovary syndrome in young adolescents (experience of a specialized pediatric endocrinology consultation)
    
    ea0110ep942
  - Pharmacological approach to neonatal hyperbilirubinemia
    
    ea0110ep943
  - Beyond weight: the quality of life in young women living with obesity
    
    ea0110ep944
  - Impact of B vitamin intake on weight loss outcomes in obese patients
    
    ea0110ep945
  - Regional prevalence of underweight, overweight and obesity in adults from 1999 to 2023 at their first endocrinological examination: a retrospective cross-sectional study performed in liguria, italy
    
    ea0110ep946
  - Evaluation of childhood obesity management in primary care setting
    
    ea0110ep947
  - Significance of liver enzyme assessment in women with metabolic dysfunction-associated liver disease, obesity, newly diagnosed type 2 diabetes, and hypertension
    
    ea0110ep948
  - Demographic, hereditary, and environmental factors in the development of masld among type 2 diabetes mellitus patients
    
    ea0110ep949
  - A resource for practical food portions for children and adults with prader-willi syndrome
    
    ea0110ep950
  - Severe hypertriglyceridemia in an infant during COVID-19 episode: case report
    
    ea0110ep951
  - Recurrent hypoglycemia in persistent hypoglycemia hyperinsulinism of infancy post near total pancreatectomy
    
    ea0110ep952
  - Physical activity among the healthcare providers at ibn rochd university hospital in casablanca
    
    ea0110ep953
  - Relationship of iodine concentration in urine with muscle mass and reaction speed in young adults
    
    ea0110ep954
  - Management of obesity and diabetes mellitus type 2 in psoriatic arthritis
    
    ea0110ep955
  - Congenital hyperinsulinism: first 18F-DOPA PET/CT scan performed in kazakhstan
    
    ea0110ep956
  - Uncommon side effects of uncommon drug: hydroxychloroquine-induced hypoglycaemia in a patient with multisystem lupus
    
    ea0110ep957
  - Adjustment of medication in patients with nasogastric tube or gastrostomy
    
    ea0110ep958
  - Therapeutic adherence to antihypertensive treatment in type 2 diabetes: barriers to achieving blood pressure targets
    
    ea0110ep959
  - Homozygous familial hypercholesterolemia: a rare case in a multiple pregnancy
    
    ea0110ep960
  - A rare case of idiopathic ketotic hypoglycemia in a child from kazakhstan
    
    ea0110ep961
  - Relationship renin-angiotensin ratio with hypertension and disease duration in patients with type 2 diabetes mellitus
    
    ea0110ep962
  - Interim analysis of equol producer prevalence in the isoflavone study
    
    ea0110ep963
  - Microbiota and obesity: current state and outlook
    
    ea0110ep964
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    ea0110ep965
  - Floating-harbor syndrome in a 39-year-old patient: description of a rare obesity clinical case
    
    ea0110ep966
  - Real-world effect of tirzepatide: a prospective observational study
    
    ea0110ep967
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    ea0110ep968
  - Clinical profile of obese adolescents
    
    ea0110ep969
  - Biological findings of obese adolescents
    
    ea0110ep970
  - Metabolic risk factors in overweight women with polycystic ovary syndrome: results of a tunisian study
    
    ea0110ep971
  - Hemoglobin levels as a potential predictor of sarcopenia in obese patients
    
    ea0110ep972
  - The impact of obesity on the clinical manifestations of early menopause in women
    
    ea0110ep973
  - Management of obesity in children and young adolescents with type 2 diabetes
    
    ea0110ep974
  - Association between overweight/obesity and iron deficiency among non-pregnant women of reproductive age in yerevan, armenia
    
    ea0110ep975
  - Height loss with age in adults with prader willi syndrome may result in artifactual increases in BMI
    
    ea0110ep976
  - The Relationship between morning blood pressure surge, serum antimullerian hormone level and homa-ir score in patients with polycystic ovary syndrome
    
    ea0110ep977
  - A case with porphyria presenting with episodic hypertension and tachycardia mimicking pheochromocytoma
    
    ea0110ep978
  - Relevance of growth differentiation factor 15 in weight management
    
    ea0110ep979
  - Impact of neurodegeneration on GLUT4 activity in experimental dm rats brain hyppocampus
    
    ea0110ep980
  - Influence of vitamin d deficiency in patients with obesity on thyroid gland and liver function
    
    ea0110ep981
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    ea0110ep982
  - Success rates of pre-pregnancy and gestational obesity interventions in preventing childhood obesity: a comprehensive review
    
    ea0110ep983
  - Lactic acidosis secondary to metformin toxicity :a case report
    
    ea0110ep984
  - Prevalence and associated factors of obesity among smokers
    
    ea0110ep985
  - Assessment of anthropometric and body composition parameters of diabetologists pan india
    
    ea0110ep986
  - Metabolic disorders in patients with polyvascular disease according to the KAMMA register
    
    ea0110ep987
  - Risk factors for metabolic disorders in patients with polycystic ovary syndrome
    
    ea0110ep988
  - Role of spermidine in longevity
    
    ea0110ep989
  - Metabolic syndrome and cancer metabolic syndrome and cancer
    
    ea0110ep990
  - Severe form of lipoedema and obesity, therapeutic challenge: report of a rare case
    
    ea0110ep991
  - Clinical case of hypothalamic obesity following craniopharyngioma removal
    
    ea0110ep992
  - Determinants of advanced non-alcoholic fatty liver disease steatosis in the obese women: results of a tunisian study
    
    ea0110ep993
  - Impact of SGLT-2 inhibitors on metabolic and cardiovascular health: a comparative analysis of patients with and without diabetes
    
    ea0110ep994
  - Evaluation of patients undergoing bariatric surgery: our experience
    
    ea0110ep995
  - Impact of respiratory function (FEV₁) on disease progression and mortality in patients with als: association with bioelectrical and biochemical parameters
    
    ea0110ep996
  - Understanding 'controlled obesity': perspectives of people with obesity on a new classification
    
    ea0110ep997
  - Relationship of iodine concentration with inflammatory and anthropometric characteristics and body composition in young adults
    
    ea0110ep998
  - GLP-1 receptor agonists and management of diabetes mellitus 2 and obesity in multiple sclerosis
    
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  - The relationship between insulin resistance, BMI, free testosterone and estradiol levels in male adults and adolescents
    
    ea0110ep1000
  - Home parenteral nutrition: experience in a tertiary hospital
    
    ea0110ep1001
  - Clinical and biological aspects of malnutrition in adults
    
    ea0110ep1002
  - Cardiovascular risk profile and achievement of therapeutic targets in patients with diabetes mellitus
    
    ea0110ep1003
  - Rapid ultrasound measurement of preperitoneral abdominal fat at detection of (NASH) in obese children's evolution of this new strategy after 2 years follow up
    
    ea0110ep1004
  - Overweight and obesity among healthcare professionals in tunisia: prevalence and associated factors
    
    ea0110ep1005
  - Elevated liver enzymes in a patient with obesity and sleep-related eating disorder during semaglutide therapy
    
    ea0110ep1006
  - Linkage between obesity and bone metabolism
    
    ea0110ep1007
  - A case report of Familial hypercholesterolemia
    
    ea0110ep1008
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    ea0110ep1009
  - Assessment of physical activity levels among paramedical staff: a cross-sectional study
    
    ea0110ep1010
  - Personalized diagnosis of obesity types using the typeobese bot
    
    ea0110ep1011
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  - Endothelial function and diabetes complications in patients with T2DM after coronary stent placement
    
    ea0110ep1013
  - Obesity as a chronic refractory to treatment disease which may be dealt with successfully
    
    ea0110ep1014
- Multisystem Endocrine Disorders
- - Optic disc drusen: an exceptional manifestation of pseudohypoparathyroidism
    
    ea0110ep1015
  - The impact of 1-hour plasma glucose on the metabolic characteristics and pregnancy outcomes in polycystic ovary syndrome
    
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  - Continuous glucose monitoring in patients with cushing's syndrome, before and after surgical therapy
    
    ea0110ep1017
  - Bridging the gap: a comprehensive analysis of adolescent PCOS treatments and outcomes across decades
    
    ea0110ep1018
  - Does hormonal cross-talk exists between different endocrine glands: an indian prospective study of this unique phenomenon
    
    ea0110ep1019
  - Synchronous pheochromocytoma and papillary thyroid carcinoma - is CACNA1H the culprit?
    
    ea0110ep1020
  - Co-existence of type 1 diabetes mellitus, thyroid dysfunction, and myasthenia gravis: a case report
    
    ea0110ep1021
  - A clinical case of a patient with alstrom's disease in the practice of an endocrinologist
    
    ea0110ep1022
  - Hormonal impacts of energy drinks on adolescents: a comprehensive review
    
    ea0110ep1023
  - Hereditary xerocytosis and secondary haemochromatosis - a rare cause of progressive endocrine dysfunction
    
    ea0110ep1024
  - Pseudohypoparathyroidism due to GNAS inactivation: a case report
    
    ea0110ep1025
  - Unraveling biological determinants of advanced fibrosis risk in type 2 diabetes patients with MASLD
    
    ea0110ep1026
  - Autoimmune polyendocrine syndrome type 1 or acquired immunodeficiency syndrome? a complex case of type 1 diabetes, hypoparathyroidism, and hiv infection
    
    ea0110ep1027
  - Hypercortisolemia and its impact on type 2 diabetes
    
    ea0110ep1028
  - A rare coexistence of auto-immune diabetes mellitus with collagenous colitis and scleroderma: a case report
    
    ea0110ep1029
  - Unexplained recurrent paronychia: a closer look at an overlooked diagnosis
    
    ea0110ep1030
  - The role of MRI and ferriscan in diagnosing and managing endocrine and growth complications in thalassemia major
    
    ea0110ep1031
  - The Unique features of growth and endocrine changes in patients with sickle sz-thalassemia
    
    ea0110ep1032
  - Unravelling the connection: papillary thyroid carcinoma in MEN1 syndrome
    
    ea0110ep1033
  - Growth and puberty of children living HIV/AIDS in a reference service in northeastern brazil
    
    ea0110ep1034
  - Primary adrenal insufficiency in a patient with type 1 diabetes
    
    ea0110ep1035
  - Management of hyperandrogenism in hemodialysis patient with PCOS: challenges and therapeutic strategies
    
    ea0110ep1036
  - Multiple endocrine and non-endocrine tumors in a patient with type 1 multiple endocrine neoplasia
    
    ea0110ep1037
  - Neurofibromatosis type 1 with polycystic liver disease and hypertension in the young as a co-occurrence with heterozygotic PKHD1 variant: a case report and review of the literature
    
    ea0110ep1038
  - Association of diabetes mellitus, primary hypothyroidism, and addison's disease in a patient followed for glycogen storage disease type iii
    
    ea0110ep1039
  - Primary hyperparathyroidism and autoimmune diseases: a case report
    
    ea0110ep1040
  - Late diagnosis and course of the treatment of patient with pseudohypoparathyroidism type 1 A and growth hormone deficiency with excellent height outcome
    
    ea0110ep1041
  - Primary hypoparathyroidism and hashimoto's thyroiditis- a rare autoimmune disease combination
    
    ea0110ep1042
  - Beyond the triad: surgical management of endocrine and skeletal complications in mccune-albright syndrome
    
    ea0110ep1043
  - Effects of intensive iron chelation therapy on glucose abnormalities in beta-thalassemia major patients
    
    ea0110ep1044
  - Hereditary primary hyperparathyroidism is still challenging - beyond genetic screening
    
    ea0110ep1045
  - Surgical management, diagnostic challenges, and long-term outcomes in a patient with MEN1: a unique case report
    
    ea0110ep1046
  - Multiple endocrine neoplasia type 1 phenotype with negative genetics
    
    ea0110ep1047
  - Clinical case report: rare association of MEN2B syndrome and type 1 diabetes
    
    ea0110ep1048
  - The [ldquo]4 A[rdquo] syndrome: a rare etiology of adrenal insufficiency in pediatric endocrinology: about a case report
    
    ea0110ep1049
  - Prader-willi syndrome: a 17-year retrospective study on clinical features and genetic findings
    
    ea0110ep1050
  - Endocrinology and immunology: exploring their intersection in autoimmune disorders
    
    ea0110ep1052
  - A case history of prader-willi syndrome: 20 years observation period
    
    ea0110ep1053
  - Hyperthyroidism and thrombosis of a varicocele: an unexpected linka case report
    
    ea0110ep1054
  - Neuromyelitis optica and endocrine comorbidities: a case report
    
    ea0110ep1055
  - Assessment of bone health, psychological wellbeing and clinical spectrum in turner syndrome: experience from a tertiary healthcare centre from north india
    
    ea0110ep1056
  - Association of primary hyperparathyroidism and papillary thyroid carcinoma in a patient with brown tumor and parkinsonism
    
    ea0110ep1057
  - Factors influencing linear growth in children with beta-thalassemia major: a comprehensive review of studies (2000-2025)
    
    ea0110ep1058
  - The critical role of pituitary imaging in sickle cell disease: insights into growth and endocrine dysfunction
    
    ea0110ep1059
  - Impact of iron deficiency anemia on growth and endocrine functions: reversibility with treatment
    
    ea0110ep1060
  - Graves disease of pubertal age associated with DIDMOAD (wolfram)syndrome
    
    ea0110ep1061
  - Therapeutic difficulties in the treatment of a girl with primary hypoparathyroidism
    
    ea0110ep1062
  - Atypical marfan syndrome (MFS) in a pediatric endocrinology practice
    
    ea0110ep1063
  - POEMS sy-a rare etiology of endocrinopathy
    
    ea0110ep1064
  - The impact of endocrine diseases on mental health
    
    ea0110ep1065
  - Endocrine and metabolic diseases associated with stress
    
    ea0110ep1066
- Pituitary, Neuroendocrinology and Puberty
- - Early detection of adrenal insufficiency after pituitary surgery: basal cortisol levels
    
    ea0110ep1067
  - Toxic pneumonitis in the context of cabergoline treatment
    
    ea0110ep1069
  - Analysis of miR 16-5p, miR 143-3p and miR 423-5p in patients with invasive non-functioning pituitary adenomas and prolactinomas
    
    ea0110ep1070
  - Early cardiovascular and metabolic benefits of rhGH therapy: positive changes in biomarkers and oxidative stress in adult-onset growth hormone deficiency
    
    ea0110ep1071
  - Remission post endoscopic pituitary surgery for cushing's disease - experience of a regional tertiary centre in UK
    
    ea0110ep1072
  - Recovery of gonadal axis in patients with prolactinomas
    
    ea0110ep1073
  - Adiposity trajectories and predictors of obesity in patients with childhood-onset craniopharyngioma
    
    ea0110ep1074
  - Cannulated prolactin test: a diagnostic approach to moderate hyperprolactinemia
    
    ea0110ep1075
  - Celebral salt wasting syndrome in a patient with known central diabetes insipidus on the background of mcap overgrowth syndrome
    
    ea0110ep1076
  - Challenging management of electrolyte imbalances in neurosurgical patient: cerebral salt wasting case report
    
    ea0110ep1077
  - Pituitary apoplexy: epidemiology, presentation and outcomes - a population-based study in malta
    
    ea0110ep1078
  - Arginine vasopressin resistance - rare clinical cases
    
    ea0110ep1080
  - Clinical case of arginine vasopressin resistance associated with a new mutation in the AVPR2 gene
    
    ea0110ep1081
  - Longitudinally assessed sex-typed play behaviour and its association with androgen levels during minipuberty in full-term and preterm children
    
    ea0110ep1082
  - MRI findings in girls with central precocious puberty: a comparative study with control group and their association with pubertal diagnosis and progression
    
    ea0110ep1083
  - Novel score of autonomic dysregulation in children with hypothalamic syndrome
    
    ea0110ep1084
  - Decoding insulinomas: clinical insights and treatment pathways
    
    ea0110ep1085
  - Neurohypophysitis in a pediatric patient with autoimmune hepatitis
    
    ea0110ep1086
  - Tolosa-Hunt syndrome?
    
    ea0110ep1087
  - The iron key to adolescence: impact of chronic iron deficiency anemia on pubertal hormones, timing, and growth"
    
    ea0110ep1088
  - Osilodrostat use in severe pediatric cushing's syndrome: short term outcomes in a case of pituitary adenoma
    
    ea0110ep1089
  - Pituitary abscess as a rare cause of multi-hormonal pituitary insufficiency and vasopressin deficiency (AVP-D, diabetes insipidus)
    
    ea0110ep1090
  - Age-related differences in clinical features of central precocious puberty: insights from a portuguese cohort
    
    ea0110ep1091
  - Gastric neuroendocrine tumors: a case series
    
    ea0110ep1092
  - Copeptin levels at baseline and in response to short-acting GLP-1 receptor agonists in patients with endogenous hyperinsulinaemic hypoglycaemia and healthy controls - a secondary analysis
    
    ea0110ep1094
  - Treatment-resistant gh-secreting pituitary adenoma in young patient harboring a variant somatic mutation of the gnas gene: a case report
    
    ea0110ep1095
  - Assessment of NF-κB levels in acromegalic patients with hepatosteatosis
    
    ea0110ep1096
  - Assessment of liver steatosis and fibrosis in acromegaly
    
    ea0110ep1097
  - Natural history and clinical behaviour of non-operated rathke's cleft cysts: a single-centre retrospective review
    
    ea0110ep1098
  - Relationship between disease severity and puberty status in pediatric systemic lupus erythematosus (SLE) patients
    
    ea0110ep1099
  - Triple hormone secreting pituitary macroadenoma: a rare cas
    
    ea0110ep1100
  - A real-world study of lanreotide autogel for the treatment of patients with acromegaly in china: baseline interim analysis
    
    ea0110ep1101
  - Misdiagnosed pituitary adenoma in a reproductive age woman
    
    ea0110ep1102
  - Pituitary metastases: a case series
    
    ea0110ep1103
  - Neurocognitive and neuropsychological assessment in the acromegalic patient: correlation with clinical, biochemical and prognostic features
    
    ea0110ep1104
  - Endoscopic endonasal treatment in patients with crooke's cell adenomas
    
    ea0110ep1106
  - AIP variants among adult patients with acromegaly
    
    ea0110ep1107
  - Granular cell tumor of the pituitary gland - an exceedingly rare diagnosis
    
    ea0110ep1108
  - Outcomes and challenges in the treatment of prolactinomas in young adults: a retrospective study of clinical and genetic factors
    
    ea0110ep1109
  - Pituitary adenomas and differentiated thyroid cancer. keys to good management: a case series
    
    ea0110ep1110
  - Resistant prolactinomas: a retrospective insights into clinical, imaging, and demographic characteristics in the largest patient cohort
    
    ea0110ep1111
  - The assessment of relationship between acromegaly and hedonic hunger
    
    ea0110ep1112
  - The challenges of managing AVP deficiency in pregnancy with hyperemesis gravidarum
    
    ea0110ep1113
  - Treatment with aromatase inhibitor in a patient with a leydig cell tumor: case report
    
    ea0110ep1114
  - Prostatic enucleation causing pituitary apoplexy in a patient with a pre-existing non-functional macroadenoma
    
    ea0110ep1115
  - Comparison between testosterone and gonadotropin treatment in adolescent males with hypogonadotropic hypogonadism
    
    ea0110ep1117
  - Clinical case of central pontine and extrapontine myelinolysis development due to severe hyponatremia
    
    ea0110ep1118
  - Rare association of lentigo and normosmic congenital isolated hypogonadotropic hypogonadism, diagnosed in mini-puberty: clinical case report
    
    ea0110ep1119
  - Advanced malignant insulinoma: when everything else fails, treatment with 177Lu-DOTATATE comes to the rescue
    
    ea0110ep1120
  - Abnormal uterine bleeding due to von willebrand disease (experience of a specialized pediatric endocrinology consultation)
    
    ea0110ep1121
  - Incidental finding of prolactinoma in a patient initially diagnosed with osteosarcoma: a case report
    
    ea0110ep1122
  - Hyperprolactinaemia: clinical presentation and dopamine agonist side effects
    
    ea0110ep1123
  - Longitudinal assessment of growth velocity, IGF-I and fasting insulin in relation to pubertal timing in healthy boys
    
    ea0110ep1124
  - Arginine vasopressin deficiency in a baby with variant of uncertain significance found in the PCSK1 gene
    
    ea0110ep1125
  - A case of multiple neuroendocrine tumors in MEN1: cushing's disease, prolactinoma, and multiple pancreatic NETS including insulinoma
    
    ea0110ep1126
  - The role of IGF-1 in monitoring prolactinoma patients: paradox or additional diagnosis?
    
    ea0110ep1127
  - Outcome of two closely spaced postcesarean pregnancies in a patient with prolactinoma: a case report
    
    ea0110ep1128
  - Assessing pubertal suppression with 3.75 mg monthly vs. 11.25 mg three-monthly leuprolide acetate in girls with central precocious puberty
    
    ea0110ep1129
  - Diagnosis of cushing's disease by desmopressin stimulated bilateral inferior petrosal sinus sampling: a case report
    
    ea0110ep1131
  - Unveiling hypothalamic syndrome, beyond obesity: diagnostic challenges and management strategies in pediatric patients - a report of 2 cases
    
    ea0110ep1132
  - A single-center experience of the effect of triptorelin on final height in girls with precocious or early puberty
    
    ea0110ep1133
  - The impact of turner syndrome and hypogonadism on brain and hypothalamic-pituitary structure: effects of treatment with sex steroids and growth hormone
    
    ea0110ep1134
  - Comparative models of acromegaly: a north american cohort of 4620 cats with presumed feline hypersomatotropism (acromegaly)
    
    ea0110ep1135
  - Concomitant development of central diabetes insipidus and cerebral salt-wasting syndrome in a child with subarachnoid hemorrhage
    
    ea0110ep1136
  - Long-term follow-up is needed in primary-like hypophysitis: a late diagnosis of Langerhans cell histiocytosis case report
    
    ea0110ep1137
  - Dealing with pituitary invaders: a corticotroph macroadenoma case
    
    ea0110ep1138
  - A rare case of pituitary adenoma co-secreting ACTH and GH
    
    ea0110ep1139
  - Familial isolated pituitary adenomas (FIPA): screening for mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene
    
    ea0110ep1140
  - Clinical management and therapeutic options for pancreatic insulinomas - a case series
    
    ea0110ep1141
  - A case of aggressive corticotropinoma in a patient after combined treatment
    
    ea0110ep1142
  - Giant prolactin-secreting pituitary adenoma: a case report
    
    ea0110ep1143
  - Autoimmune hypophysitis induced by Anti-PDL1 therapy
    
    ea0110ep1144
  - Acute total visual loss complicating macroprolactinoma apoplexy
    
    ea0110ep1145
  - Endocrinological evaluation and natural course of symptomatic paediatric patients with rathke cleft cysts
    
    ea0110ep1146
  - Real-world characteristics and treatment patterns of adults receiving long-acting growth hormone: insights from the INSIGHTS-GHT registry
    
    ea0110ep1147
  - Aggressive pituitary tumours and carcinomas - clinicopathological data and treatment experiences from Hungary
    
    ea0110ep1148
  - Central precocious puberty in a female child with a giant hypothalamic hamartoma: diagnosis and treatment
    
    ea0110ep1149
  - Rathke's cleft cyst presenting with isolated arginine vasopressin deficiency
    
    ea0110ep1150
  - Osilodrostat effectiveness in the treatment of cushing's disease (CD) and ectopic cushing's syndrome (ECS)- a single-center real-life experience
    
    ea0110ep1151
  - GH secretion inhibition test in children - should we use different standards for obese children vs. normal weight children?
    
    ea0110ep1152
  - Prolonged adrenal insufficiency following osilodrostat discontinuation
    
    ea0110ep1153
  - Body composition analysis in children treated with recombinant GH
    
    ea0110ep1154
  - Impact of early menarche on adolescent health
    
    ea0110ep1155
  - Case report of ependymal pituicytoma
    
    ea0110ep1156
  - Not just the skin rash: a case of coexistence of macroprolactinoma and metastatic neuroendocrine tumour
    
    ea0110ep1157
  - A rare coexistence of acromegaly with metastatic adrenocortical carcinoma
    
    ea0110ep1158
  - A diagnosis not to be missed
    
    ea0110ep1159
  - Peripheral precocious puberty leading to central precocious puberty due to ovarian sex cord stromal tumor with annular tubules (SCTAT)
    
    ea0110ep1160
  - BMI impacts on quality of life and endocrine complications in patients with non-functioning pituitary adenomas - A prospective study in patients before and after transsphenoidal surgery
    
    ea0110ep1161
  - Recurrent primary pituitary abscesses in a young girl: a rare clinical challenge
    
    ea0110ep1162
  - Germinoma of the suprasellar region: 2 cases report
    
    ea0110ep1163
  - Ventriculoperitoneal shunting and diabetes insipidus
    
    ea0110ep1164
  - Clinical features of primary empty sella
    
    ea0110ep1165
  - Metabolic disorders and prolactin-secreting adenomas in men
    
    ea0110ep1166
  - Pituitary macroadenoma in the menopause may be a prolactinoma?
    
    ea0110ep1167
  - A hazard of transitional endocrine care
    
    ea0110ep1168
  - Validity of adult height prediction methods (bayley pinnaue charts and bonexpert) in indian children with idiopathic short stature
    
    ea0110ep1169
  - Pre-treatment differentiation between non-functioning pituitary adenomas and prolactinomas based on serum prolactin levels
    
    ea0110ep1170
  - Radiological evaluation of central nervous system in children with gonadotropin-dependent precocious puberty
    
    ea0110ep1171
  - Analysis of pituitary tumors in a single center in slovakia
    
    ea0110ep1172
  - Ectopic cushing's syndrome due to a pulmonary NET: diagnostic challenges and the need for a multidisciplinary approach
    
    ea0110ep1173
  - A rare etiology of autoimmune hypophysitis
    
    ea0110ep1174
  - Calcitonin-secreting neoplasm of the lung: a case report
    
    ea0110ep1175
  - FIPA-AIP positive pituitary gigantism: post-surgical remission
    
    ea0110ep1176
  - Transient arterial hypertension developed during therapy with triptorelin in a girl with central precocious puberty
    
    ea0110ep1177
  - Assessment of comorbidity resolution after long-term acromegaly remission
    
    ea0110ep1178
  - Usefulness of serial prolactin measurement to confirm the presence of hyperprolactinemia
    
    ea0110ep1179
  - Prevalence of sexual dysfunction in patients with pituitary disease: insights from the international DREAMS survey study
    
    ea0110ep1180
  - A case of leydig cell tumor presenting with peripheral precocious puberty
    
    ea0110ep1181
  - The association of neutrophil/HDL ratio, plasma atherogenic index and several cardiovascular risk scoring systems in acromegaly
    
    ea0110ep1182
  - Impact of somatostatin analogues on glycaemic control in patients with neuroendocrine tumours: a retrospective observational study
    
    ea0110ep1183
  - A case report on timely surgical intervention in pituitary apoplexy and cavernous sinus invasion
    
    ea0110ep1184
  - Surgical management of pituitary adenoma: a single-centre experience
    
    ea0110ep1185
  - A retrospective study of clinicopathological features of growth hormone and prolactin co-secreting pituitary tumors
    
    ea0110ep1186
  - Clinical results in an aggressive coricotroph adenoma with a unique molecular expression profile expressing high levels of different oncogenic splicing variants (SSTR5TMD4, In1-ghrelin and GHRH-R)
    
    ea0110ep1187
  - A fifteen-year-old boy with GH/PRL-secreting pituitary neuroendocrine tumor without excessive height growth
    
    ea0110ep1188
  - Late onset isolated corticotrope deficiency induced by pembrolizumab
    
    ea0110ep1189
  - The pituitary stone: a rare prolactinoma find
    
    ea0110ep1190
  - Meningeal syndrome revealing craniopharyngioma of the sellar region: a case report
    
    ea0110ep1191
  - Treatment of acromegaly patients with resistance to first-generation somatostatin receptor ligands (fg-SRLs)
    
    ea0110ep1192
  - Indexes of liver steatosis and fibrosis in metabolically associated fatty liver in hypopituitarism
    
    ea0110ep1193
  - Therapeutic challenges in male patients with prolactin-secreting pituitary adenomas
    
    ea0110ep1194
  - Endocrine-related adverse events in patient receiving combined immune checkpoint inhibition - a case report
    
    ea0110ep1195
  - Anterior pituitary deficiencies: a descriptive study in a pediatric hospital in cameroon
    
    ea0110ep1196
  - Adrenal crisis after missed diagnosis of pituitary sarcoidosis: a case report
    
    ea0110ep1197
  - Is partial empty sella or empty sella a risk factor for visual field defects?
    
    ea0110ep1198
  - GnRH analogs in pediatric practice: efficacy, safety, and side effects—a comprehensive review
    
    ea0110ep1199
  - Cushing's disease and severe resistant hypertension: surgical challenges due to rare kissing carotids
    
    ea0110ep1200
  - Evaluation of alexithymia and quality of life in patients with acromegaly
    
    ea0110ep1201
  - Aggressive prolactinoma with failed temozolomide therapy: management strategies & literature review
    
    ea0110ep1202
  - Systematic review of cardiometabolic outcomes in young people with gender dysphoria and the impact of puberty blockers
    
    ea0110ep1203
  - Obstructive sleep apnea in patients with acromegaly
    
    ea0110ep1204
  - Case report: infectious hypophysitis as a complication of sphenoiditis
    
    ea0110ep1205
  - A rare case of TSH-oma in a frail patient: diagnostic and therapeutic challenges
    
    ea0110ep1206
  - Comparison of normetanephrine and metanephrine secretion in pheochromocytoma: clinical and radiological features
    
    ea0110ep1207
  - A comparative analysis of three positron emission tomography tracers in a patient with residual acromegaly
    
    ea0110ep1208
  - Associations between central diabetes insipidus and brain mri findings: a comprehensive analysis in a large cohort with extensive clinical experience
    
    ea0110ep1209
  - A rare association between pituicytoma and cushing's syndrome
    
    ea0110ep1210
  - Adverse hepato-biliary-pancreatic events in acromegaly patients treated with first generation somatostatin analogues: an italian multicenter study
    
    ea0110ep1211
  - Clinico-radiological correlation analysis of a cohort of 50 children with pituitary stalk interruption syndrome
    
    ea0110ep1212
  - Cabergoline therapy in adolescent cushing's disease: hypercortisolism improvement with persistent tumor
    
    ea0110ep1213
  - Bilateral achilles tendon rupture: a rare presentation of cushing's disease
    
    ea0110ep1214
  - Giant prolactinoma in adult males
    
    ea0110ep1215
  - When hormones disagree: a case of elevated ACTH with normal cortisol and suspected macro-ACTH
    
    ea0110ep1216
  - Thyrotropin deficiency and transient central adrenal insufficiency with anterior pituitary hypoplasia in an infant with neurofibromatosis-noonan syndrome
    
    ea0110ep1217
  - Case Report: SIAD caused by LGI-1 antibody encephalitis
    
    ea0110ep1218
  - Sheehan's syndrome revealed by profound hypothyoidism: a case report
    
    ea0110ep1219
  - Rheumatological manifestations of acromegaly: a report of 78 cases
    
    ea0110ep1220
  - Genotype-negative MEN 1 - limitations of genetic testing
    
    ea0110ep1221
  - A clinical case of infective endocarditis in a patient with acromegaly: impact on biochemical markers
    
    ea0110ep1222
  - Home capillary monitoring of sodium in a patient with adipsic diabetes insipidus
    
    ea0110ep1223
  - Is the coexistence of acromegaly with primary empty sella syndrome rare?
    
    ea0110ep1224
  - A case of hypophysitis successfully treated by corticotherapy: a diagnostic challenge with germinoma in a 5-year-old chil
    
    ea0110ep1225
  - A complex case of growth hormone deficiency and pituitary mass in an adolescent girl
    
    ea0110ep1226
  - TSH-secreting pituitary macroadenoma: a case report and therapeutic considerations
    
    ea0110ep1227
  - Pituitary stalk interruption syndrome as a cause of central hypothyroidism, growth hormone deficiency and hypogonadotropic hypogonadism: a case report
    
    ea0110ep1228
  - Autoimmunity in a patient with prolactinoma: coincidence or consequence?
    
    ea0110ep1229
  - Clinical features and metabolic risk in girls with premature adrenarche
    
    ea0110ep1230
  - Development of empty sella in neurosarcoidosis; a case report
    
    ea0110ep1231
  - A case of spontaneous remission of active pituitary macroadenoma
    
    ea0110ep1232
  - Aggressive somatotropinoma: collaborative management by endocrinologists and oncologists
    
    ea0110ep1233
  - A case of nonfunctioning pituitary macroadenoma - 7 year follow-up after transsphenoidal surgery and radiation therapy
    
    ea0110ep1234
  - Clinical and therapeutic management of hypopituitarism during pregnancy in a patient with PROP1-related combined pituitary hormone deficiency
    
    ea0110ep1235
  - Anthropometric or biochemical markers to predict the onset of menarche
    
    ea0110ep1236
  - [ldquo]Whispering[rdquo] cushing syndrome: presentation of three cases
    
    ea0110ep1237
  - Acromegaly and metabolic complications: a report of 78 cases
    
    ea0110ep1238
  - Pituitary apoplexy complicated by subarachnoid hemorrhage: the role of stress and cabergoline therapy
    
    ea0110ep1239
  - Co-occurrence of tuberous sclerosis and pituitary stalk interruption syndrome: a rare clinical presentation
    
    ea0110ep1240
  - A case of cushing disease presenting with pituitary apoplexy in an adolescent female
    
    ea0110ep1241
  - Analysis of obesity frequency in girls with central precocious puberty
    
    ea0110ep1242
  - Copeptin and MR-proADM, do not show the risk of cardiometabolic disease in patients with acromegaly—preliminary results
    
    ea0110ep1243
  - Prevalence and clinical characteristics of central precocious puberty: experience of single academic center in Serbia
    
    ea0110ep1244
  - Fenestrated pituitary infundibulum in a young woman with ehlers-danlos syndrome: a case report
    
    ea0110ep1245
  - Why was the hypopituitary patient's life not saved?
    
    ea0110ep1246
  - Diagnostic challenges in polyuria-polydipsia syndrome: a case from resource-limited setting
    
    ea0110ep1247
  - Delayed diagnosis of pituitary apoplexy in a patient with migraine
    
    ea0110ep1248
  - Management of macroprolactinomas during pregnancy: about 2 cases
    
    ea0110ep1249
  - Non functional pituitary macroadenoma expressing GH, LH and ACTH
    
    ea0110ep1250
  - Discordant disease activity indicators in a patient with acromegaly
    
    ea0110ep1251
  - Delayed diagnosis of pituitary apoplexy: a case report
    
    ea0110ep1252
  - More than thirst: diagnosis of central diabetes insipidus in a young woman without comorbidities
    
    ea0110ep1253
  - A persistent headache in acromegalic patient: the positive result of combination therapy with pasireotide LAR, pegvisomant and cabergoline
    
    ea0110ep1254
  - Giant macroprolactinoma mimicking a craniopharyngioma: a remarkable evolution with persistent hyperprolactinemia due to big big prolactin
    
    ea0110ep1255
  - Effects of abnormal growth hormone secretion treatment on bone metabolism and structure in acromegaly and adult growth hormone deficiency-a preliminary report
    
    ea0110ep1256
  - Sarcoidosis diagnosis after succesful treatment of cushing's disease
    
    ea0110ep1257
  - Multidisciplinary approach in the management of cardiac metastasis from small intestinal neuroendocrine tumour: a case report
    
    ea0110ep1258
  - Radiotherapy as first line therapy for pituitary adenomas
    
    ea0110ep1259
  - Symptomatic rathke's cleft cyst
    
    ea0110ep1260
  - Immune checkpoint inhibitor-induced hypophysitis: a case report of panhypopituitarism and acute neurological manifestations
    
    ea0110ep1261
  - Unmasking the giant: a pediatric macroprolactinoma mimicking a craniopharyngioma
    
    ea0110ep1262
  - A case report of an infant with congenital hypopituitarism presenting with hypoglycemia and low beta-hydroxybutyrate
    
    ea0110ep1263
  - Delayed puberty: the coin other side
    
    ea0110ep1264
  - First report of a case of post-surgical pituitary neuroendocrine tumor residue confined within the pituitary stalk
    
    ea0110ep1265
  - A rare case report of an intravascular large B-cell lymphoma causing a panhypopituitarism
    
    ea0110ep1266
  - The First genetically confirmed case of wolfram syndrome in the philippines - a case report
    
    ea0110ep1267
  - Hormonally inactive pituitary adenomas: clinical and laboratory features and predictors of surgical treatment effectiveness
    
    ea0110ep1268
  - The overlooked iceberg in hyponatremia in the elderly: the pituitary gland The overlooked iceberg in hyponatremia in the elderly: the pituitary gland
    
    ea0110ep1269
  - An unsual case of hypopituitarism coincidental with rasmussen's encephalitis and rathke's cleft cyst
    
    ea0110ep1270
  - AVP deficiency secondary to herbal remedies
    
    ea0110ep1271
  - Secondary corticotropic insufficiency due to arachnoid cyst: a reversibility to explore"
    
    ea0110ep1272
  - Misdiagnosis: a case of craniopharyngioma revealed by diabetes insipidus
    
    ea0110ep1273
  - A case of metastatic PITNET. diagnosis, treatment and outcomes
    
    ea0110ep1274
  - Combining hormone replacement therapy and adjuvant treatment for a patient with resistant prolactinoma: a new clinical strategy
    
    ea0110ep1275
  - A case of arginine vasopressin deficiency following immunization with mrna-covid-19 vaccination
    
    ea0110ep1276
  - Unusual endocrine trio: a case report of down syndrome with autoimmune hypothyroidism and prolactinoma
    
    ea0110ep1277
  - Contribution of MRI in the diagnosis of puitary stalk interruption syndrome
    
    ea0110ep1278
  - A clinical case: chromosomal abnormalities and hypogonadism
    
    ea0110ep1279
  - Psychosis as a rare clinical presentation of sheehan syndrome: case report and review of the literature
    
    ea0110ep1280
  - Cushing's disease due to invasive macroadeoma with crooke cellular transformation and mgmt methylation
    
    ea0110ep1281
  - Kallmann-morsier syndrome: a genetic mystery behind amenorrhea and anosmia
    
    ea0110ep1282
  - Acromegaly and kidney cancer what is the link?
    
    ea0110ep1283
  - Height blood pressure and acromegaly: about 78 cases
    
    ea0110ep1284
  - Parhon's syndrome: the difficult path to finding the root cause
    
    ea0110ep1285
  - Metyrapone as a bridge therapy after pituitary radiation for aggressive Cushing's disease: a case report
    
    ea0110ep1286
  - Combined therapy of somatostatin analogue with pegvisomant for the management of acromegaly
    
    ea0110ep1287
  - Barriers to timely diagnosis of cushing's disease in the outpatient setting
    
    ea0110ep1288
  - The interplay of hormones and neuroplasticity: how hormonal changes shape brain adaptation to stress and learning
    
    ea0110ep1289
  - Corticotherapy revealing a pituitary adenoma
    
    ea0110ep1290
  - Craniopharyngioma in adolescence: from diagnosis to ongoing care
    
    ea0110ep1291
  - Non-surgical management of patients with pituitary macroadenomas: case report
    
    ea0110ep1292
- Reproductive and Developmental Endocrinology
- - The relationship between reproductive hormones, testis size, mating strategy, and spermatogenesis efficiency across primates
    
    ea0110ep1293
  - Characterization of intracrine androgen production in human genital skin fibroblasts
    
    ea0110ep1297
  - Reproductive hormones in 46, XY differences/disorders of sex development and healthy populations
    
    ea0110ep1298
  - Evaluating the FIB-4 score as a screening tool for NAFLD in PCOS: a cross-sectional study
    
    ea0110ep1299
  - Evolution in the health-care demand at the transgender care unit of malaga after 25 years of experience
    
    ea0110ep1300
  - The impact of gender dysphoria diagnosis on parents of transgender youth: the role of heteronormativity and mentalization
    
    ea0110ep1301
  - Mental health assessment in women with PCOS: evaluating anxiety and depression using GAD-7 and PHQ-9
    
    ea0110ep1302
  - Leptin levels may not have a role in the development of pubertal gynecomastia
    
    ea0110ep1303
  - Long term pubertal outcome of patients with prenatal diagnosis of ovarian cysts
    
    ea0110ep1304
  - The impact of thyroid autoimmunity on clinical outcomes in euthyroid women undergoing ART: a systematic review
    
    ea0110ep1305
  - Spironolactone repurposing in the management of benign premature adrenarche with facial acne
    
    ea0110ep1306
  - Efficacy of preoperative hormonal treatment in severe cases of hypospadias: a case-control study
    
    ea0110ep1307
  - Evaluation of cardiovascular risks in people with gender dysphoria who received gender-affirmig hormone therapy
    
    ea0110ep1309
  - Safety of puberty blockers and testosterone therapy for cardiovascular health in adolescents with gender dysphoria
    
    ea0110ep1310
  - Circulating adipokine concentrations aid in distinguishing functional hypothalamic amenorrhoea and polycystic ovary syndrome in women presenting with oligo/amenorrhoea
    
    ea0110ep1311
  - Pharmaceutical disruption of steroidogenesis
    
    ea0110ep1312
  - The role of autocrine androgen signalling for leydig cell function
    
    ea0110ep1313
  - Fertility information needs in adult survivors of childhood cancer - first results of the FeProCAYA study
    
    ea0110ep1314
  - Effect of FSH therapy on semen parameters in male idiopathic infertility: a real-life experience
    
    ea0110ep1315
  - Impact of thyroid autoantibodies on ovarian reserve and embryo quality in euthyroid women undergoing assisted reproductive technology
    
    ea0110ep1316
  - Body proportions, hypothalamic-pituitary-gonadal function, testicular morphology and the risk for gonadal malignancy in males with 46,XX testicular DSD and 47,XXY Klinefelter syndrome
    
    ea0110ep1317
  - What can we learn from the largest north african cohort of testicular disorders of sex development?
    
    ea0110ep1318
  - Genotype-phenotype correlation of patients with androgen insensitivity syndrome: a cohort study including 9 families
    
    ea0110ep1319
  - Impact of gender-affirming hormone therapy on cardiovascular risk in transgender individuals
    
    ea0110ep1320
  - Raised sex hormone binding globulins levels in men: a retrospective observational study
    
    ea0110ep1321
  - Free testosterone and shbg play independent roles in insulin resistance and metabolic alterations of women with pcos
    
    ea0110ep1322
  - Severe obstructive sleep apnea syndrome and continuous positive airways pressure therapy impact on testosterone levels in male patients with severe obesity
    
    ea0110ep1323
  - Alteration of the tryptophan concentrations in women with polycystic ovary syndrome (PCOS)
    
    ea0110ep1324
  - Semen cryopreservation and semen quality in transfeminine adolescents prior to hormone therapy
    
    ea0110ep1325
  - Temporal trends in serum testosterone and luteinizing hormone levels indicate an ongoing resetting of hypothalamic-pituitary-gonadal function in healthy men: a systematic review
    
    ea0110ep1326
  - Circulating gut hormone concentrations in women presenting with menstrual disturbance
    
    ea0110ep1327
  - Primary amenorrhea secondary to [beta]-thalassemia major: a case report
    
    ea0110ep1328
  - Androstenedione method comparison of three automated immunoassays and ID-LC-MS/MS in routine testing and disorders of steroid synthesis
    
    ea0110ep1329
  - The impact of gender dysphoria on mental health of transgender and gender non-conforming patients - 7-year of experience in the first gender unit for youth in poland
    
    ea0110ep1330
  - Comparison of metabolic outcomes in lean and obese women with polycystic ovary syndrome
    
    ea0110ep1331
  - Evaluation of thyroid hormone sensitivity in polycystic ovary syndrome
    
    ea0110ep1332
  - Physical growth of chinese girls' menarche onset
    
    ea0110ep1333
  - Ovarian suppression using GnRH analog followed by estrogen and progestin for the classic form of lipoid congenital adrenal hyperplasia: A case report and its implications for ovarian morphology
    
    ea0110ep1334
  - Evaluating olfactory and gustatory function in patients with hypogonadotropic hypogonadism
    
    ea0110ep1335
  - Primary gonadal dysfunction after oncological treatment in a cohort of childhood medulloblastoma survivors
    
    ea0110ep1336
  - A novel de novo mutation of the DHX37 gene in patients with 46,XY DSD
    
    ea0110ep1337
  - Exercise habits and activity levels in an international sample of people with PCOS
    
    ea0110ep1338
  - Ten-year experience of a referral center for transgeneder and gender diverse children and adolescents in north-east of italy
    
    ea0110ep1339
  - Complete androgen insensitivity syndrome (CAIS) management: balancing malignancy risk, hormonal benefits, and patient autonomy
    
    ea0110ep1340
  - Pregnancy in patients with a history of oncological diagnosis in the childhood-juvenile stage
    
    ea0110ep1341
  - A rare case of a child with a 46XY disorder of sex development with multiple congenital anomalies
    
    ea0110ep1342
  - Polycystic ovary syndrome: what we know about it?
    
    ea0110ep1343
  - Diabetic turner syndrome patients - conclusions from the bulgarian diabetes registry
    
    ea0110ep1344
  - Etiologic distribution of adult-onset male hypogonadism in the modern era: retrospective cohort study from finnish tertiary center
    
    ea0110ep1345
  - Obstetrical outcomes after oocyte donation in turner syndrome: retrospective study among patients with primary ovarian insufficiency
    
    ea0110ep1346
  - Case report of a newborn child with dsd due to 46,XX/46,XY chimerism
    
    ea0110ep1347
  - RAB5B Gene expression and its association with insulin resistance in women with PCOS
    
    ea0110ep1348
  - The role of triglyceride-glucose index in women with polycystic ovary syndrome: a systematic review and meta-analysis
    
    ea0110ep1349
  - Bone mineral density and trabecular bone score in adolescents and young women with primary ovarian insufficiency
    
    ea0110ep1350
  - Transitioning care in hypogonadism: a retrospective analysis
    
    ea0110ep1351
  - Psychosomatic outcomes in adulthood among north african patients with testicular DSD
    
    ea0110ep1352
  - The effect of gender-affirming hormone therapy on the occurrence of axial spondyloarthritis in people with gender dysphoria
    
    ea0110ep1353
  - Evaluation of test results according to body mass index of patients who had a gnrh stimulation test with a preliminary diagnosis of precocious puberty
    
    ea0110ep1355
  - Multidisciplinary team (MDT) clinics for children and young people with differences in sex development (DSD): evaluation of clinical outcomes and patient/caregivers' experiences
    
    ea0110ep1356
  - Thyroid status of women in preparation for in vitro fertilization
    
    ea0110ep1357
  - Time is testicular: early cryptorchidism care to avert tumors
    
    ea0110ep1358
  - Anti mullerian trends after aGnRH initiation in trans boys adolescents
    
    ea0110ep1359
  - Association between folic acid levels and physiological and developmental indicators in children with developmental delays
    
    ea0110ep1360
  - Yoga intervention effects on metabolic profiles in polycystic ovary syndrome: plasma metabolomics analysis
    
    ea0110ep1361
  - Clinical, biochemical, instrumental and genetic evaluation of a group of patients with hypogonadotropic hypogonadism
    
    ea0110ep1362
  - Differences of sexual development - a portuguese single-center case series of the last 24 years
    
    ea0110ep1363
  - Neuroanatomical insights into gender identity: the role of hypothalamic subregions in therapy-naive transgender individuals
    
    ea0110ep1364
  - Leydig cell ovarian tumor in initially normal sized ovaries - a case report
    
    ea0110ep1365
  - Primary amenorrhea in adolescents: a deep dive into the causes and characteristics
    
    ea0110ep1366
  - Bridging endocrinology and genetics: uncovering familial partial lipodystrophy type 2 in an adolescent with primary amenorrhea
    
    ea0110ep1367
  - Biochemical hyperandrogenism: a diagnostic pitfall
    
    ea0110ep1368
  - Sociodemographic and metabolic profiling of transgender and gender diverse treatment-naive adolescents - seven-year experience in the first gender unit dedicated to youth in poland
    
    ea0110ep1369
  - Cabergoline treatment reduces androgen levels and restores menstrual cycles in women with hyperprolactinemic polycystic ovary syndrome
    
    ea0110ep1370
  - Circulating anti-mullerian hormone and inhibin b levels in reproductive disorders causing oligo/amenorrhoea
    
    ea0110ep1371
  - Beyond genetics: exploring the challenges of diagnosis and management in 46xy disorders of sex development
    
    ea0110ep1372
  - Mutations in MSH5 in primary ovarian insufficiency in adolesent: a case report
    
    ea0110ep1373
  - Case report and literature review: a 46,xx infant with atypical genitalia diagnosed with primary ovarian insufficiency (POI) caused by hfm1 gene variants
    
    ea0110ep1374
  - Efficacy of oral testosterone undecanoate in children with androgen insensitivity syndrome
    
    ea0110ep1375
  - Clinical profile and biomolecular assessment of a group of patients suspected 46 xy dsd in an african setting
    
    ea0110ep1376
  - Demographic and psychosocial characterisation of transgender and gender-diverse youngsters referred to the danish gender identity service
    
    ea0110ep1377
  - [alpha]-reductase type 2 deficiency- are there early predictors for gender identity outcome?
    
    ea0110ep1378
  - Epidemiological, clinical and etiological aspects of acne in adult women
    
    ea0110ep1379
  - A case report of aromatase deficiency
    
    ea0110ep1380
  - When hyperandrogenism hides more: a sertoli-leydig cell tumor in a 16-year-old girl
    
    ea0110ep1381
  - The importance of the NR5A1 gene in sexual differentiation
    
    ea0110ep1382
  - Increased alpha-glucosidase levels in sertoli cell-only syndrome: a report of three cases
    
    ea0110ep1383
  - Endocrine factors in the development of recurrent pregnancy loss clinical case
    
    ea0110ep1384
  - The relationship between indicators of leptin and anti-Muller hormone in women suffering from infertility and obesity
    
    ea0110ep1385
  - Unusual pulmonary embolism under testosterone replacement therapy in male hypogonadism: a case report
    
    ea0110ep1386
  - A case of 46, xy dsd: pubertal virilization and gender identity in 17szhsd3 deficiency
    
    ea0110ep1387
  - Clinical profile of turner syndrome patients in a tertiary endocrine center in Nepal
    
    ea0110ep1388
  - Star protein deficiency in clinical practice: [ldquo]a case series review[rdquo]
    
    ea0110ep1389
  - Italian survey on the endocrinological clinical approach to polycystic ovary syndrome
    
    ea0110ep1390
  - Gynecomastia as a potential late effect of testicular lymphoma treatment: a case report
    
    ea0110ep1391
  - Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report
    
    ea0110ep1392
  - Pure gonadal dysgenesis (46 XX type): 2 cases report
    
    ea0110ep1393
  - Complexities of complete androgen insensitivity syndrome
    
    ea0110ep1394
  - Experiences in setting up a transitional care process in patients with differences in sex development and congenital adrenal hyperplasia in a tertiary care centre of a low-middle-income country
    
    ea0110ep1395
  - Clinical hyperandrogenism in obese and non-obese women with polycystic ovary syndrome
    
    ea0110ep1396
  - Syndromic gonadal dysgenesis: a rare case of image syndrome
    
    ea0110ep1397
  - From ovary to testis: a case of 46,XX ovotesticular DSD
    
    ea0110ep1398
  - Unilateral drug induced gynecomastia secondary to antiretroviral therapy in an HIV infected patient
    
    ea0110ep1399
  - Primary amennorhea caused by hyperandrogenism due to porto-systemic shunting
    
    ea0110ep1400
  - From prolactinoma suspicion to fmr1 premutation: a case of overlapping endocrine disorders
    
    ea0110ep1401
  - Impact on fertility and bone mass of triptorelin and estradiol therapy in trans girls
    
    ea0110ep1402
  - Premature ovarian insufficiency in a 26-year-old patient treated with hydroxyurea for sickle cell disease
    
    ea0110ep1403
  - The Puzzle Of 45,X/46,XY mosaicism (MGD): insights from an adult male case report
    
    ea0110ep1404
  - Gender affirmation and hormonal health: the role of testosterone therapy in a non-binary cis woman with primary ovarian insufficiency
    
    ea0110ep1405
  - Challenges in managing persistent hypercalcemia during pregnancy after failed surgical intervention: a multidisciplinary approach?
    
    ea0110ep1406
  - Type 2 diabetes and hypogonadism: unveiling werner syndrome in a young adult
    
    ea0110ep1407
  - Mixed gonadal dysgenesis: a case report and management approach
    
    ea0110ep1408
  - Molecular analysis of AMH and AMHR2 genes in four cases of persistent mullerian duct syndrome (PMDS)
    
    ea0110ep1409
  - Morbid obesity in a patient with a Y chromosome microdeletion
    
    ea0110ep1410
  - Adoloscent girl with secondary amenorrhoea due to adult granulosa cell tumour - A rare presentation
    
    ea0110ep1411
  - Unusual case of hirsuitism following isotretinoin therapy for acne
    
    ea0110ep1412
  - Clinical and diagnostic aspects of diminished ovarian reserve in women with thyroid hypofunction
    
    ea0110ep1413
  - Should all women with PCOS be treated for insulin resistance? absolutely, but we should know what PCOS is
    
    ea0110ep1414
  - Isolated fsh deficiency in man with lujan-fryns syndrome (LFS)
    
    ea0110ep1415
  - Swyer syndrome in a young adult with type 1 diabetes presenting with primary amenorrhea: a case report
    
    ea0110ep1416
  - Steroid metabolome signature of transgender and gender diverse treatment-naive adolescents - 7-year experience in the first gender unit dedicated to youth in Poland
    
    ea0110ep1417
  - From diagnosis to adulthood: navigating the complexities of a 46,XX SRY-positive male with DSD
    
    ea0110ep1418
  - Primary amenorrhoea revealing prader-willi syndrome: a case report
    
    ea0110ep1419
  - Impact of hysterectomy on ovarian function and woman health
    
    ea0110ep1420
  - Effect of growth hormone to spinal growth and recombinant
    
    ea0110ep1421
  - Leg ulcer and klinefelter's syndrome: cause or coincidence? a case report
    
    ea0110ep1422
  - A rare case of coexisting turner syndrome and mayer-rokitansky-kuster-hauser syndrome
    
    ea0110ep1423
  - An atypical case of premature pubarche
    
    ea0110ep1424
  - Aromatase defficiency: a rare cause of female ambiguous genetalia
    
    ea0110ep1425
- Thyroid
- - Warthin-like subtype of papillary thyroid cancer - a single-center experience, preliminary report
    
    ea0110ep1426
  - Serum proteomic analysis reveals insights into the mechanism of action of teprotumumab, an insulin-like growth factor-1 receptor inhibitor, in patients with chronic thyroid eye disease (TED)
    
    ea0110ep1427
  - Comparison of hematologic and autoimmune status of patients with Graves' disease and autoimmune thyroiditis during surgical treatment
    
    ea0110ep1428
  - The role of procalcitonin and ProGRP in the follow-up of medullary thyroid carcinoma
    
    ea0110ep1429
  - Resection of the thyroid isthmus as a surgical treatment method for well-differentiated thyroid cancer in selected patients
    
    ea0110ep1430
  - Medullary thyroid carcinoma: a 15-year case series
    
    ea0110ep1431
  - Cardiovascular and metabolic markers after thyroid cancer treatment: a fine balance of long-term outcomes
    
    ea0110ep1432
  - The value of intraoperative frozen section in surgical management of thyroid nodules
    
    ea0110ep1433
  - Radioiodine-refractory differentiated thyroid cancer in children and adolescents: a retrospective single-center study
    
    ea0110ep1434
  - The role and limitations of fine-needle aspiration cytology in thyroid nodule diagnosis
    
    ea0110ep1435
  - A problem necessitating a reemphasized solution: a case of hypothyroidism presenting as a new pericardial effusion in a patient with helicobacter pylori infection treated with proton-pump inhibitor
    
    ea0110ep1436
  - Thyroid nodules in acromegaly: a study of 78 cases
    
    ea0110ep1437
  - Report of two cases of thyroid hormone resistance syndrome with developmental disorders in young children
    
    ea0110ep1438
  - An unusual case of a patient alternating from hypothyroidism to hyperthyroidism following COVID-19 infection
    
    ea0110ep1439
  - Chemotherapy-induced hypothyroidism: a crucial diagnostic challenge
    
    ea0110ep1440
  - Hyperthyroidism and pregnancy: specificities of the first trimester
    
    ea0110ep1441
  - Synchronous papillary thyroid cancer and malignant neoplasms: Hodgkin lymphoma and nasopharyngeal carcinoma
    
    ea0110ep1442
  - Recurrent thyroid-associated ophthalmopathy in hashimoto's thyroiditis: a case report
    
    ea0110ep1443
  - Hormonal effects of the thyroid gland in breast cancer chemotherapy
    
    ea0110ep1444
  - Surgical treatment of grave's disease in children: a report of five cases
    
    ea0110ep1445
  - Primary hyperparathyroidism in a 12-year old girl caused by an ectopic mediastinal adenoma: a case report
    
    ea0110ep1446
  - Fahr's syndrome: the hidden neurological face of hypocalcemia
    
    ea0110ep1447
  - Do patients with Ehlers-Danlos syndrome and a history of fractures have abnormal thyroid hormone profiles?
    
    ea0110ep1448
  - A single-center experience with papillary thyroid carcinoma arising from a thyroglossal duct cyst
    
    ea0110ep1449
  - Steroid-responsive encephalopathy in graves' disease: a rare case of neuropsychiatric symptoms in thyroid autoimmunity
    
    ea0110ep1450
  - Routine clinical analysis of BRAFV600E and TERT promoter variants in advanced thyroid carcinomas
    
    ea0110ep1451
  - Thyroid cancers in children: pathological and therapeutic specificities
    
    ea0110ep1452
  - Relationship between high bone turn over and tsh receptor antibodies in patients newly diagnosed with Graves' disease
    
    ea0110ep1453
  - Thyroglossal duct cysts: diagnosis and management
    
    ea0110ep1454
  - Long-term follow-up of nodular goiter - experience in fukushima area of north-east Japan
    
    ea0110ep1455
  - Vitamin D supplementation to prevent post-thyroidectomy hypocalcemia
    
    ea0110ep1456
  - Trends of thyroglobulin and dynamic risk stratification in thyroid nodule cancer without radioiodine ablation
    
    ea0110ep1457
  - Growth profiles in children with congenital primary hypothyroidism before and after the relaunching of newborn screening programme in dr soetomo hospital
    
    ea0110ep1458
  - A case with TSHB gene mutation presenting with neuromotor retardation
    
    ea0110ep1459
  - Harmonization of thyroid function test measurements across multiple immunoassay platforms for a common reference interval
    
    ea0110ep1460
  - Characteristics of papillary thyroid carcinoma in men
    
    ea0110ep1461
  - Endocrine surveillance: detecting recurrent graves' disease in ectopic thyroid and primary hyperparathyroidism post-radioiodine treatment
    
    ea0110ep1462
  - Synchronous medullary and papillary thyroid carcinoma: a clinical case
    
    ea0110ep1463
  - Evaluation of the relapse rate in patients with graves disease and its relationship to the great score
    
    ea0110ep1464
  - Celiac disease in patients with thyroid disorders: clinical features, diagnosis, and management
    
    ea0110ep1465
  - A decade of thyroid orbitopathy research in albania: a retrospective study from a tertiary referral center
    
    ea0110ep1466
  - Prevalence of thyroid nudules in children with idiopathic prcocious puberty or early and fast puberty
    
    ea0110ep1467
  - Influence of aromatase inhibitors on thyroid function in postmenopausal women with early-stage breast cancer: a prospective controlled study
    
    ea0110ep1468
  - Thyroid hormone levels and echocardiographic changes in subclinical hypothyroidism: a correlation study
    
    ea0110ep1469
  - Effectiveness of antithyroid therapy on TH1, TH17, and TH22 lymphocytes in pediatric Graves' patients
    
    ea0110ep1470
  - Paresthesia as a rare symptom of thyrotoxicosis following parathyroidectomy
    
    ea0110ep1471
  - Recent advances in the treatment of goiterous hypothyroidism in infants and children
    
    ea0110ep1472
  - Assessment of subacute thyroiditis progression using shear wave elastography
    
    ea0110ep1473
  - Non-autoimmune subclinical hypothyroidism associated with variants in the PAX8 gene: presentation of two patients
    
    ea0110ep1474
  - Hypothyroidism manifesting as delusional ideas of persecution: a case report
    
    ea0110ep1475
  - Association of plasma thyroxine levels with cognitive disorders in early-onset schizophrenia and other psychosis spectrum disorders
    
    ea0110ep1476
  - Evaluation of clinical findings, laboratory results, and radiological features in pediatric patients followed up for thyroid dysfunction
    
    ea0110ep1477
  - Effectiveness and outcome of fixed 600 Mbq radioactive iodine activity in the treatment of benign thyroid disease
    
    ea0110ep1478
  - Metabolically associated fatty liver disease in woman with hypothyroidism
    
    ea0110ep1479
  - P63 immunohistochemical peculiarities under autoimmune thyroiditis vs papillary thyroid carcinoma (PTC)
    
    ea0110ep1480
  - Papillary thyroid microcarcinomas detected by nuclear medicine imaging methods do they have a worse prognosis?
    
    ea0110ep1481
  - Corneal ulcer, a rare complication of hashimoto's thyroiditis
    
    ea0110ep1482
  - Acute thyrotoxic crisis with cardiothyreosis: management challenges in the face of carbimazole-induced hepatic cytolysis
    
    ea0110ep1483
  - Vesicular thyroid carcinomas
    
    ea0110ep1484
  - Sclerotherapy of cystic formations of the thyroid and parathyroid glands
    
    ea0110ep1485
  - Ultrasound support of diapeutic interventions in thyrioid pathology
    
    ea0110ep1486
  - Prevalence of thyroid autoimmunity and by age, sex, geographic region, and socioeconomic status among 1.7 million chinese adults
    
    ea0110ep1487
  - A case of post-operative graves disease
    
    ea0110ep1488
  - AI chatbots vs endocrinologists in clinical decision-making in thyroid nodule and papillary thyroid carcinoma management
    
    ea0110ep1489
  - HPA axis integrity after Iv methylprednisolone for active moderate-to-severe thyroid eye disease
    
    ea0110ep1490
  - Differentiated high-grade thyroid carcinoma (DHGTC) and poorly differentiated TC (PDTC): diagnostic and therapeutic challenges in the precision medicine era - report of two cases
    
    ea0110ep1491
  - Hypothyroidism in infants and young children: diagnostic challenges and clinical manifestations
    
    ea0110ep1492
  - Graves' disease in monozygotic twins: a case report and literature review
    
    ea0110ep1493
  - The value of ultrasound features and elastography in the diagnosis of medullary thyroid carcinoma
    
    ea0110ep1494
  - The quest for reliable biomarkers: circulating free DNA in thyroid cancer
    
    ea0110ep1495
  - Autoimmune thyrogastric syndrome: clinical features, diagnosis, and management
    
    ea0110ep1496
  - Dozens of doubts: a series of atypical presentations of medullary thyroid carcinoma running title: atypical presentations of medullary thyroid carcinoma
    
    ea0110ep1497
  - Low risk of malignancy in thyroid nodules at our centre
    
    ea0110ep1498
  - Peculiarities of diagnostic gluten intolerance in ukrainian patients with autoimmune thyroiditis
    
    ea0110ep1499
  - Unusual presentation of hypothyroidism: pericardial effusion is not always due to cardiac cause
    
    ea0110ep1500
  - Assessing sensitivity of thyroglobulin measurement in neck node fine needle washout for diagnosis of thyroid cancer metastasis: use of node dissection and 131I scintigraphy as reference standards
    
    ea0110ep1501
  - Thyroid disease related to the SARS-CoV-2 virus
    
    ea0110ep1502
  - Post-alemtuzumab thyroid autoimmunity remitting after commencement of ocrelizumab in patients with multiple sclerosis
    
    ea0110ep1503
  - T cell gene expression differences between ATA+ infertile euthyroid and ATA+ hypothyroid patients
    
    ea0110ep1504
  - Genetic testing in medulary thyroid cancer in a tertiary center in Romania
    
    ea0110ep1505
  - years of experience in providing surgical care to children with nodular and diffuse toxic goiter
    
    ea0110ep1506
  - Iratherapy and graves' disease: about 20 cases followed
    
    ea0110ep1507
  - Hashimoto's thyroiditis or graves' disease? a case of thyroid autoimmune disease with oscillating thyroid function
    
    ea0110ep1508
  - Myxedema coma triggered by a urinary tract infection: a case report
    
    ea0110ep1509
  - Toxic thyroid nodule and anterior pituitary insufficiency: a rare association
    
    ea0110ep1510
  - Challenges in the diagnosis of thymic hyperplasia-associated myasthenia gravis in the setting of coexisting Graves' disease
    
    ea0110ep1511
  - Pre-operative lugol's iodine treatment in the management of patients undergoing thyroidectomy for graves' disease: is there an impact?
    
    ea0110ep1512
  - Autoimmune thyroid disease: a continuum oscillating between hypothyroidism and hyperthyroidism: a case report
    
    ea0110ep1513
  - Thyroid disorders in autoimmune polyendocrinopathy
    
    ea0110ep1514
  - Optimizing thyroid surgery: the critical role of intraoperative histological examination
    
    ea0110ep1515
  - Secondary hyperparathyroidism and papillary carcinoma of the thyroid: about a case
    
    ea0110ep1516
  - Association of graves' disease and differentiated thyroid cancer: a report of two cases
    
    ea0110ep1517
  - A challenging case of amiodarone induced thyrotoxicosis
    
    ea0110ep1518
  - Apalutamide-induced severe hypothyroidism in a patient treated with levothyroxine: new data on the impact of apalutamide on thyroid hormone metabolism
    
    ea0110ep1519
  - Acute suppurative thyroiditis due to internal fistula: a paediatric case report
    
    ea0110ep1520
  - "Predictive value evaluation of preoperative sonographic risk stratification in patients with differentiated thyroid cancer: a feasibility study for a prospective clinical trial"
    
    ea0110ep1521
  - Utilization of blood cell-derived parameters in the diagnosis of subacute thyroiditis during pregnancy
    
    ea0110ep1522
  - Adherence to levothyroxine treatment among patients withhypothyroidism and evaluation of depressive stratus andfactors related with non-adherence
    
    ea0110ep1523
  - Severe graves' disease presenting with supraventricular tachycardia (SVT) in a 54-year-old male smoker
    
    ea0110ep1524
  - Approaches for improving diagnostics precision, treatment anh monitoring relapse of graves' disease in national children's hospital
    
    ea0110ep1525
  - Paralyzed by potassium: the thyroid's sneaky trick
    
    ea0110ep1526
  - What is the role of Pro-inflammatory biomarkers in Hashimoto's thyroiditis?
    
    ea0110ep1527
  - Predictive factors of relapse, TED, and thyroidectomy in graves' disease
    
    ea0110ep1528
  - From neurology to endocrinology: an atypical case of thyroid storm in a young adult
    
    ea0110ep1529
  - Thyroid function test assay interference: biochemical and clinical challenges and its implications
    
    ea0110ep1530
  - Risk of obstructive sleep apnea in patients with clinical hypothyroidism based on STOP-BANG score
    
    ea0110ep1531
  - Pancreatic mass during follow-up of a papillary thyroid microcarcinoma: lenvatinib's side effect, metastasis or primary tumor ?
    
    ea0110ep1532
  - Papillary thyroid carcinoma treated with vandetanib
    
    ea0110ep1533
  - Middle-aged women thyroid gland ultrasound assessment in the minsk-city
    
    ea0110ep1534
  - A rare case of thyrotropinoma inappropriately treated as Graves' disease
    
    ea0110ep1535
  - Levothiroxine malabsorbtion
    
    ea0110ep1536
  - Lost and found: a thyroid tale of tissues gone rogue
    
    ea0110ep1537
  - Dysphagia in old age, what if it's an ectopic thyroid?: a case report
    
    ea0110ep1538
  - Cross-reactions between synthetic antithyroid drugs
    
    ea0110ep1539
  - Rare coexistence of parathyroid adenoma and thyroid adenomas: a case report
    
    ea0110ep1540
  - Residual thyroid tissue post-thyroidectomy: a hidden driver of Graves' disease
    
    ea0110ep1541
  - Case report: graves' disease after hemithyroidectomy
    
    ea0110ep1542
  - Hypercalcemia secondary to postlaryngectomy thyroiditis: a case report
    
    ea0110ep1543
  - Riedel's thyroiditis: a diagnosis not to be overlooked
    
    ea0110ep1544
  - Thyroid surgery in children: Indications and outcomes
    
    ea0110ep1545
  - Etiological insights into autoimmune hypothyroidism
    
    ea0110ep1546
  - Prevalence and caracteristics of thyroid carcinoma in patients having Hashimoto's thyroiditis
    
    ea0110ep1547
  - Association of papillary and medullary thyroid carcinoma: a report of 3 cases
    
    ea0110ep1548
  - Navigating the thin line of risks and benefits: a case of nivolumab-induced hypothyroidism in a patient with metastatic melanoma
    
    ea0110ep1549
  - Challenges to implement thyroid cancer guidelines for thyroid surgeons of Bangladesh
    
    ea0110ep1550
  - Thyroid tissue in a cervical lymph node is not always malignant: A case report
    
    ea0110ep1551
  - Pitfalls in the management of a palpable pediatric thyroid nodule: a case report
    
    ea0110ep1552
  - Shear wave elastography (SWE) in the evaluation of thyroid tissue in children and adolescents with autoimmune thyroiditis
    
    ea0110ep1553
  - Common but unexpected autoimmune endocrine disorders in pregnancy - case reports
    
    ea0110ep1554
  - Outcomes of thyroid lobectomy in bethesda v and vi nodules: a clinical analysis
    
    ea0110ep1555
  - Comprehensive summary of studies on goiterous hypothyroidism in infants and children: patient characteristics, treatment, and prognosis"
    
    ea0110ep1556
  - Unraveling MEN syndrome: how genetic testing illuminates complex family histories and improves patient outcomes
    
    ea0110ep1557
  - A rare case of palpation thyroiditis following parathyroidectomy
    
    ea0110ep1558
  - Thyroid eye disease following total thyroidectomy in a complex case of graves' disease with reaction to antithyroid therapy
    
    ea0110ep1559
  - Thyroid function replacement time after total and subtotal thyroidectomy
    
    ea0110ep1560
  - Total thyroidectomy for Graves' disease in a patient with down syndrome and glycogen storage disease type ia
    
    ea0110ep1561
  - Parapharyngeal cystic lymph node metastasis revealing differentiated thyroid microcarcinoma
    
    ea0110ep1562
  - Follicular adenoma with follicular epithelial dysplasia-a care report
    
    ea0110ep1563
  - Pazopanib in radioiodine refractory follicular thyroid carcinoma. a case report
    
    ea0110ep1564
  - Pemphigus vulgaris and Graves' disease
    
    ea0110ep1565
  - Uncommon presentation of thyroid-associated orbitopathy in hypothyroidism: a case report
    
    ea0110ep1566
  - Primary thyroid lymphoma in hashimoto's thyroiditis: a case report and review of the association and diagnostic approach
    
    ea0110ep1567
  - Hypokalemic periodic paralysis in hyperthyroidism: a rare endocrine emergency
    
    ea0110ep1568
  - Thyroid association ophthalmopathy in hashimoto's thyroiditis: a case report
    
    ea0110ep1569
  - Surgical treatment of plunging goiters: challenges for ENT specialists
    
    ea0110ep1570
  - Atypical testicular germ cell cancer metastasis in the thyroid: a case report of a very rare clinical presentation
    
    ea0110ep1571
  - Autonomous resolution of a toxic thyroid nodule: a case report
    
    ea0110ep1572
  - Levothyroxine absorption test: practical application. Importance of the clinical laboratory in the diagnosis of refractory hypothyroidism. A case report
    
    ea0110ep1573
  - Dual autoimmune thyroid disease: a case of simultaneous Graves' disease and hashimoto's thyroiditis
    
    ea0110ep1574
  - Liquid biopsy in the molecular diagnosis of metastatic medullary thyroid cancer - case report
    
    ea0110ep1575
  - Diffuse malignancies of the thyroid - clinical cases
    
    ea0110ep1576
  - Non-graves orbitopathy in a patient with hypothyroidism, hashimoto's thyroiditis, and hiv on combined antiretroviral therapy
    
    ea0110ep1577
  - Metastatic medullary cancer treated with Sorafenib: Service experience
    
    ea0110ep1578
  - Discordance between clinic, biology and ultrasound in the diagnosis of Graves' disease: contribution of scintigraphy in a case report
    
    ea0110ep1579
  - Osteoporose radiale: une complication rare du traitement suppressif du carcinome papillaire de la thyroide
    
    ea0110ep1580
  - Unilateral ptosis in a patient with thyroid eye disease: A case report
    
    ea0110ep1581
  - Adverse effects of hyperthyroidism therapies: insights from a clinical cohort
    
    ea0110ep1582
  - Siblings sharing disorder; familial papillary thyroid carcinoma
    
    ea0110ep1583
  - Immunotherapy-associated thyroid dysfunction during breast cancer treatment
    
    ea0110ep1584
  - An uncommon cause of hyperthyroidism - gestational trophoblastic neoplasia
    
    ea0110ep1585
  - Evolutive aspects of SUBCLINICAL hypothyroidism
    
    ea0110ep1586
  - Would you miss a thyroid storm in acute setting?
    
    ea0110ep1587
  - Internet searches for thyroid disease and impact of the world thyroid day - a global overview and a local one for Greece
    
    ea0110ep1588
  - Asymptomatic riedel's thyroiditis: a case report
    
    ea0110ep1589
  - Feisty hyperplasia - a case of aggressive parathyroid hyperplasia
    
    ea0110ep1590
  - Nes-onset diabetes as a potential clue to the early diagnosis of pancreatic cancer
    
    ea0110ep1591
  - A case of newly diagnosed thyroid hormone resistance syndrome in singapore
    
    ea0110ep1592
  - Elevated calcitonin in the absence of medullary thyroid carcinoma: a diagnostic challenge
    
    ea0110ep1593
  - Corticosteroid therapy in dysthyroid orbitopathy: tolerance and therapeutic efficacy
    
    ea0110ep1594
  - When a hot nodule turns out to be an oncocytic carcinoma
    
    ea0110ep1595
  - Growth challenges in congenital athyreosis: a case report and endocrine insights
    
    ea0110ep1596
  - Brain metastasis in a patient with oncocytic thyroid carcinoma
    
    ea0110ep1597
  - A challenging etiological diagnosis of hypothyroidism following pazopanib treatment
    
    ea0110ep1599
  - Vitiligo and its association with thyroid dysfunction and other autoimmune diseases
    
    ea0110ep1600
  - Exploring the link between universal alopecia and hashimoto's thyroiditis
    
    ea0110ep1601
  - Morphea and papillary thyroid carcinoma
    
    ea0110ep1602
  - A Case report: acute suppurative thyroiditis presenting with thyroid abscess
    
    ea0110ep1603
  - Parotid metastasis as the first presentation of papillary thyroid carcinoma: a case report
    
    ea0110ep1604
  - A vesicular carcinoma of the thyroid on Graves' disease: a rare association
    
    ea0110ep1605
  - Graves disease after radioactive iodine treated toxic adenoma
    
    ea0110ep1606
  - Challenges in managing severe T3 thyrotoxicosis: a complex case of Graves' disease with multidisciplinary intervention and surgical resolution
    
    ea0110ep1607
  - Hypoparathyroidism after total thyroidectomy: an epidemiological study
    
    ea0110ep1608
  - Recurrence of subacute thyroiditis 20 years after the first attack in two female patients
    
    ea0110ep1609
  - The plunging goiter: a report of 18 cases
    
    ea0110ep1610
  - Out of service: late-onset hypoparathyroidism
    
    ea0110ep1611
  - Endocrine follow-up during pregnancy for surgically treated medullary thyroid microcarcinoma
    
    ea0110ep1612
  - Screening for dysthyroidism in pregnant women with diabetes
    
    ea0110ep1613
  - New-onset diabetes associated with severe hyperthyroidism: a case report.
    
    ea0110ep1614
  - Failure of a contraception in graves' disease woman, a case report
    
    ea0110ep1615
  - Anaplastic thyroid carcinoma with thoracic metastases: a case report
    
    ea0110ep1616
  - Investigating the role of selenium and inositol supplementation in managing hashimoto's thyroiditis: a preliminary observational study
    
    ea0110ep1617
  - Discrepancy between cytological findings and histopathological results in thyroid nodules
    
    ea0110ep1618
  - Rare recurrence of de quervain's thyroiditis
    
    ea0110ep1619
  - De Quervain thyroiditis mimicking an aggressive thyroid malignancy
    
    ea0110ep1620
  - The impact of nighttime liothyronine and selenium supplementation on hypothyroid patient well-being and thyroid function
    
    ea0110ep1621
  - A rare presentation of hypothyreosis complicated by rhabdomyolysis and acute renal injury
    
    ea0110ep1622
  - Unveiling the causes of hyperthyroidism: a retrospective analysis
    
    ea0110ep1623
  - Echographic features of nodular hashimoto's thyroiditis
    
    ea0110ep1624

Endocrine Abstracts
ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
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Endocrine Abstracts

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

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