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Volume 113
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SFEEU2025
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Society for Endocrinology Clinical Update 2025
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0114 UKINETS2025
0113 SFEEU2025
0112 BES2025
0111 BSPED2025
0110 ECEESPE2025
0109 SFEBES2025
0108 NANETS2024
0107 IACS9
0106 BES2024
0105 UKINETS2024
0104 SFEIES24
0103 BSPED2024
0102 EYES2024
0101 ETA2024
0100 SFEEU2024
0099 ECE2024
0098 NANETS2023
0097 BES2023
0096 UKINETS2023
0095 BSPED2023
0094 SFEBES2023
0093 EYES2023
0092 ETA2023
0091 SFEEU2023
0090 ECE2023
0089 NANETS2022
0088 BES2022
0087 UKINETS2022
0086 SFEBES2022
0085 BSPED2022
0084 ETA2022
0083 EYES2022
0082 SFEEU2022
0081 ECE2022
0080 UKINETS2021
0079 BES2021
0078 BSPED2021
0077 SFEBES2021
0076 CHD2021
0075 EYES2021
0074 SFENCC2021
0073 ECE2021
0072 UKINETS2020
0071 BES2020
0070 ECE2020
0069 SFENCC2020
0068 UKINETS2019
0067 EYES2019
0066 BSPED2019
0065 SFEBES2019
0064 BES2019
0063 ECE2019
0062 EU2019
0061 OU2019
0060 UKINETS2018
0059 SFEBES2018
0058 BSPED2018
0057 BES2018
0056 ECE2018
0055 SFEEU2018
0054 NuclearReceptors2018
0053 OU2018
0052 UKINETS2017
0051 BSPED2017
0050 SFEBES2017
0049 ECE2017
0048 SFEEU2017
0047 Theranostics2016
0046 UKINETS2016
0045 BSPED2016
0044 SFEBES2016
0043 WCTD2016
0042 Androgens2016
0041 ECE2016
0040 ESEBEC2016
0039 BSPED2015
0038 SFEBES2015
0037 ECE2015
0036 BSPED2014
0035 ECE2014
0034 SFEBES2014
0033 BSPED2013
0032 ECE2013
0031 SFEBES2013
0030 BSPED2012
0029 ICEECE2012
0028 SFEBES2012
0027 BSPED2011
0026 ECE2011
0025 SFEBES2011
0024 BSPED2010
0023 BSPED2009
0022 ECE2010
0021 SFEBES2009
0020 ECE2009
0019 SFEBES2009
0018 MES2008
0017 BSPED2008
0016 ECE2008
0015 SFEBES2008
0014 ECE2007
0013 SFEBES2007
0012 SFE2006
0011 ECE2006
0010 SFE2005
0009 BES2005
0008 SFE2004
0007 BES2004
0006 SFE2003
0005 BES2003
0004 SFE2002
0003 BES2002
0002 SFE2001
Summary
Abstracts
Abstract Book
Contents
Society for Endocrinology Clinical Update 2025
Workshop A: Disorders of the hypothalamus and pituitary
Adrenal insufficiency assessment after transsphenoidal surgery: caution with SST and the recommended role of ITT - a case report
ea0113wa1.1
Acromegaly in the diabetes clinic
ea0113wa1.2
Missed diagnosis of mild autonomous cortisol secretion (MACS) in a patient with pituitary macroadenoma presenting as steroid withdrawal syndrome following transsphenoidal surgery
ea0113wa1.3
Post-operative management of salt & water disturbances: a triple-phase response to transsphenoidal surgery for craniopharyngioma
ea0113wa1.4
When erectile dysfunction hides a deeper cause: pituitary hypophysitis in a young male
ea0113wa2.1
Cyclical vs evolving cushing's disease: the diagnostic conundrum and endless investigation
ea0113wa2.2
Arginine vasopressin deficiency after craniopharyngioma surgery: a complex multidisciplinary challenge
ea0113wa2.3
Acromegaly with pituitary stalk involvement: multidisciplinary challenges in management
ea0113wa2.4
A case of panhypopituitarism
ea0113wa3.1
Unusual presentation of adrenal insufficiency with weight gain and atypical diabetes
ea0113wa3.2
A case of acromegaly, with review of perioperative monitoring for risk of hypopituitarism and disease recurrence
ea0113wa3.3
Challenges in the perioperative management of a young adult with suprasellar craniopharyngioma, panhypopituitarism, and AVP deficiency
ea0113wa3.4
Pembrolizumab-associated hypophysitis and diabetes insipidus in a patient with metastatic lung adenocarcinoma: a case report
ea0113wa4.1
Giant prolactinoma presenting with central hypopituitarism: a case of dramatic medical response
ea0113wa4.2
Severe catatonia as a rare neuropsychiatric manifestation of ACTH-dependent cushing's syndrome
ea0113wa4.3
Arginine vasopressin deficiency perioperatively in a patient with pituitary apoplexy
ea0113wa4.4
Ironing out hypogonadotropic hypogonadism - haemochromatosis affecting the pituitary gland
ea0113wa5.1
Immune checkpoint inhibitor-induced hypophysitis: a case report
ea0113wa5.2
Partial AVP deficiency following transsphenoidal surgery for cushing's disease
ea0113wa5.3
A complex case of post-operative adipsic diabetes insipidus and cognitive impairment
ea0113wa5.4
Workshop B: Disorders of growth and development
A case of partial androgen insensitivity syndrome
ea0113wb1.1
Pubertal and growth delay from chronic non-adherence to levothyroxine
ea0113wb1.2
A journey through a late presentation of hypogonadotropic hypogonadism in an 18 year old male: gonadotropin induced puberty, testicular growth and spontaneous descent
ea0113wb2.1
Reversal of primary amenorrhea with titrated Mounjaro therapy
ea0113wb2.2
[ldquo]Uterine development after pubertal induction in mosaic turner syndrome: re-evaluating apparent mullerian agenesis in hypoestrogenic states.[rdquo]
ea0113wb3.1
Primary ovarian insufficiency with severe osteoporosis in adolescence
ea0113wb4.1
A case of delayed puberty in the male secondary to hypogonadotrophic hypogonadism and partial growth hormone deficiency
ea0113wb5.1
Workshop C: Disorders of the thyroid gland
Assay interference in familial dysalbuminemic hyperthyroxinemia
ea0113wc1.1
Management challenges of subclinical hypothyroidism
ea0113wc1.2
Avoiding misdiagnosis: clinical implications of familial dysalbuminaemic hyperthyroxinaemia
ea0113wc2.1
Iatrogenic thyroid dysfunctions: two clinical cases demonstrating the jod-basedow and wolf-chaikoff effects
ea0113wc2.2
From subclinical hyperthyroidism to atrial fibrillation: the silent progression of multinodular goitre
ea0113wc2.3
When numbers lie: misleading thyroid profile due to heterophile antibody interference in a comorbid inpatient
ea0113wc3.1
An uncommon explanation of abnormal thyroid function tests: assay interference with macro-TSH
ea0113wc3.2
Elevated TSH with elevated FT3 and FT4: a diagnostic dilemma
ea0113wc3.3
A challenging case of resistance to thyroid hormone presenting with atrial fibrillation in an elderly woman
ea0113wc4.1
Macrothyrotropin as a cause of falsely elevated TSH in two clinically euthyroid patients
ea0113wc4.2
Abstract unavailable
ea0113wc4.3
Contrasting discordant thyroid function tests in a family with resistance to thyroid hormone [beta] syndrome
ea0113wc5.1
Thyroid hormones on the fence: navigating diagnostic gray zones
ea0113wc5.2
Workshop D: Disorders of the adrenal gland
Adrenal insufficiency: the critical crossroads!
ea0113wd1.1
Hypercalcaemia as the initial manifestation of addison's disease
ea0113wd1.2
Intersecting axes in non-classical cah: adrenal androgens and obesity-related hypogonadism in adulthood
ea0113wd1.3
Isolated ACTH deficiency: an unusual crisis arising from delayed diagnosis
ea0113wd2.1
Adrenal crisis in disguise: integrating biochemical, hormonal, and clinical clues
ea0113wd2.2
Diagnosis and work-up of primary adrenal insufficiency
ea0113wd2.3
Optimising glucocorticoid therapy in congenital adrenal hyperplasia: balancing acth suppression and long-term steroid-related complications
ea0113wd2.4
Co-presentation of graves' disease and addisons disease with addisonian crisis
ea0113wd3.1
A challenging case of primary adrenal insufficiency with multiple autoimmune conditions
ea0113wd3.2
Abstract unavailable
ea0113wd3.3
Unmasking adrenal suppression: a case of iatrogenic adrenal insufficiency
ea0113wd4.1
[ldquo]Beyond initial fatigue: long-term physical and psychological management in primary addison's disease[rdquo]
ea0113wd4.2
Congenital adrenal hyperplasia and infertility in men
ea0113wd4.3
Management of non-classical congenital adrenal hyperplasia across the life course
ea0113wd4.4
Successful slow weaning of long-term prednisolone in a patient with still's disease: clinical progress and ongoing management
ea0113wd5.1
Management of immunotherapy-induced adrenal insufficiency in an elderly gentleman with a background of metastatic melanoma
ea0113wd5.2
Steroid-responsive testicular masses in untreated 3[beta]-HSD deficiency: a case of misdiagnosed malignancy
ea0113wd5.3
Workshop E: Disorders of the gonads
Testosterone therapy in borderline hypogonadism and depression: a case of diagnostic ambiguity, therapeutic entrapment, and iatrogenic erythrocytosis
ea0113we1.1
Primary ovarian insufficiency presenting as primary amenorrhea in an adolescent
ea0113we1.2
Impact of misdiagnosis in hypogonadism: a case of prolonged testosterone therapy and axis recovery[rdquo]
ea0113we2.1
Late presentation of primary amenorrhoea - a diagnostic work-up
ea0113we2.2
From supplements to suppression: lessons from two cases in a general endocrine clinic
ea0113we3.1
Challenges in diagnosing male hypogonadism: a case series highlighting risks of unregulated testosterone therapy
ea0113we4.1
Diagnostic challenges in male anabolic-androgenic steroid use
ea0113we5.1
Fluctuating severe hyperandrogenism of uncertain origin in a perimenopausal female
ea0113we5.2
Workshop F: Disorders of the parathyroid glands, calcium metabolism and bone
Tertiary hyperparathyroidism in X linked hypophosphatemia: challenges and emerging therapeutic strategies
ea0113wf1.1
Selecting anabolic therapy in osteoporosis with fragility fractures
ea0113wf1.2
A journey to diagnosis: oncogenic osteomalacia presenting with recurrent fragility fractures
ea0113wf2.1
Hungry bone syndrome following delayed parathyroidectomy in a young male with symptomatic primary hyperparathyroidism and obstructive urolithiasis
ea0113wf2.2
Fibrous dysplasia should be considered a differential in asymptomatic, isolated rise in ALP
ea0113wf3.1
Starved bones: malnutrition, type 3c diabetes, and the perfect storm for osteoporosis
ea0113wf3.2
To treat or not to treat: bone health decisions post-parathyroidectomy
ea0113wf4.1
Severe hypercalcaemic crisis and high bone turnover in primary hyperparathyroidism: the role of early parathyroidectomy and the challenge of hungry bone syndrome
ea0113wf5.1
Chronic aches and pains with low ALK phosphatase
ea0113wf5.2
Workshop G: Disorders of appetite and weight
From childhood-onset obesity to adult weight reduction: multidisciplinary management of a patient with KSR2 mutation
ea0113wg1.1
Difficulty identifying clinical signs of cushing's disease with concomitant glucagon-like peptide-1 receptor (GLP-1) agonist use
ea0113wg2.1
Beyond weight loss: transforming outcomes through obesity management
ea0113wg3.1
Ethical and clinical challenges in renal transplant eligibility for a patient with prader-willi syndrome
ea0113wg4.1
Workshop H: Miscellaneous endocrine and metabolic disorders
A MEN1 family
ea0113wh1.1
Recurrent primary hyperparathyroidism during pregnancy revealing MEN1 syndrome: diagnostic and surgical challenges
ea0113wh2.1
Autosomal dominant hypocalcaemia type 1 in a family with autoimmune endocrinopathies: importance of genetic testing
ea0113wh3.1
Advanced adrenocortical carcinoma with severe hypercortisolemia-role of debulking surgery
ea0113wh4.1
A hidden syndrome behind hypertension: a case of von hippel-lindau in a young adult
ea0113wh5.1