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Volume 31
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Summary
Abstract Book
Programme
Volume Editors
eposters
Abstracts
Contents
Plenary Lecturers’ Biographical Notes
Society for Endocrinology Dale Medal Lecture
Nuclear receptors and AMPK: can exercise mimetics cure diabetes
ea0031pl1
Society for Endocrinology Dale Medal Lecture
ea0031pl1biog
Society for Endocrinology Hoffenberg International Medal Lecture
Multiple applications of intracrinology in clinical medicine
ea0031pl2
Society for Endocrinology Hoffenberg International Medal Lecture
ea0031pl2biog
Society for Endocrinology European Medal Lecture
cAMP in the pituitary: an old messenger for multiple signals
ea0031pl3
Society for Endocrinology European Medal Lecture
ea0031pl3biog
Society for Endocrinology Transatlantic Medal Lecture
Abstract unavailable
ea0031pl4
British Thyroid Association Pitt-Rivers Lecture
BTA_Pitt Rivers Lecture
ea0031pl5
Society for Endocrinology Medal Lecture
Genes and giants
ea0031pl6
Society for Endocrinology Medal Lecture
ea0031pl6biog
Clinical Endocrinology Trust Lecture
The dynamics of hypothalamo-pituitary-adrenal activity
ea0031pl7
Clinical Endocrinology Trust Lecture
ea0031pl7biog
Clinical Endocrinology Trust Visiting Professor Lecture
Abstract unavailable
ea0031pl8
Clinical Endocrinology Trust Visiting Professor Lecture
ea0031pl8biog
Symposia
Irn bru, to drink or not to drink: endocrinology and iron
Iron homeostasis: who are the major players?
ea0031s1.1
The iron-regulatory hormone hepcidin
ea0031s1.2
The celtic disease [ndash] haemochromatosis: a disease of iron overload
ea0031s1.3
Hormone Maketh Man
Anti-Mullerian hormone: a Sertoli cell hormone that can be used as a predictor of male hypogonadism
ea0031s2.1
The role of IGFs and the Sertoli cell in driving 'maleness'
ea0031s2.2
Androgens and male fertility: a long way from the black box theory
ea0031s2.3
Nurture not nature: epigenetics and disease susceptibility
A mouse model of non-genetic inter-generational effects
ea0031s3.1
Nutritional programming of epigenetics in metabolic syndrome
ea0031s3.2
Epigenetic changes associated with prenatal exposure to famine in humans
ea0031s3.3
New Bone Biology – Is there life after RANK ligand?
Abstract unavailable
ea0031s4.1
Inhibition of sclerostin in the treatment of osteoporosis
ea0031s4.2
Parathyroid hormone-related protein as a potential treatment for osteoporosis
ea0031s4.3
Abstract unavailable
ea0031s4.4
Sex in the brain (Supported by
Endocrine Connections
)
Abstract unavailable
ea0031s5.1
Abstract unavailable
ea0031s5.2
Abstract unavailable
ea0031s5.3
Hormone-dependent chromatin modifications regulating sexually differentiated animal behaviour
ea0031s5.4
Making the glucocorticoid clock run smoothly (Supported by Addison's Disease self-help group)
Monitoring glucocorticoid signaling and circadian clock function with transgenic zebrafish reporter lines
ea0031s6.1
Abstract unavailable
ea0031s6.2
Diurnal cortisol delivery: a novel tool for adrenal insufficiency
ea0031s6.3
Abstract unavailable
ea0031s6.4
Thyroid hormone receptors – mutations and implications (Supported by
Journal of Molecular Endocrinology
)
Physiologically distinct roles for thyroid hormone receptor isoforms
ea0031s7.1
Human thyroid hormone receptor alpha mutations [ndash] a novel syndrome emerges
ea0031s7.2
Human thyroid hormone receptor [beta] mutations-syndrome of resistance to thyroid hormone
ea0031s7.3
Nuclear receptor corepressors confer the actions of mutant thyroid hormone receptor [alpha]
ea0031s7.4
Non functioning pituitary tumours (Supported by
Endocrine-Related Cancer
and the Pituitary Foundation)
Epidemiology and natural history of pituitary tumours
ea0031s8.1
Abstract unavailable
ea0031s8.2
Pathological markers of aggressive pituitary tumour behaviour
ea0031s8.3
Aggressive pituitary tumours and temozolomide treatment
ea0031s8.4
Novel aspects of GPCR signalling (Supported by the
Journal of Endocrinology
)
GPCR mutations and reproduction
ea0031s9.1
Persistent signaling by TSH receptors
ea0031s9.2
In vivo dimerization of LH receptors
ea0031s9.3
Allosteric LH, TSH and FSH receptor signaling
ea0031s9.4
Lipodystrophy – The perils of being thin
Abstract unavailable
ea0031s10.1
Abstract unavailable
ea0031s10.2
HIV lipodystrophy
ea0031s10.3
Approach to lipodystrophy management: a new national service
ea0031s10.4
Guts, brains and bariatric surgery
Abstract unavailable
ea0031s11.1
Ghrelin, a gut-brain signal of importance for food reward
ea0031s11.2
Abstract unavailable
ea0031s11.3
Abstract unavailable
ea0031s11.4
Thymic function and autoimmune endocrine disease
The thymus medulla, aire and autoimmunity
ea0031s12.1
Abstract unavailable
ea0031s12.2
Thymic microenvironments for T cell repertoire formation
ea0031s12.3
Regulatory T cells, CTLA-4 and autoimmune disease
ea0031s12.4
Clinical Management Workshops
Management controversies in parathyroid disease
Abstract unavailable
ea0031cmw1.1
Abstract unavailable
ea0031cmw1.2
Abstract unavailable
ea0031cmw1.3
Medical management of primary hyperparathyroidism
ea0031cmw1.4
How Do I Do It?
Abstract unavailable
ea0031cmw2.1
How do I investigate and manage hypomagnesaemia?
ea0031cmw2.2
How do I monitor and follow up transgender patients using hormonal therapies?
ea0031cmw2.3
How do I manage the pregnant patient with a prolactinoma?
ea0031cmw2.4
How and when do I induce puberty in males?
ea0031cmw2.5
Abstract unavailable
ea0031cmw2.6
PCOS – why, how and what
Consensus on women's health aspects of PCOS
ea0031cmw3.1
Abstract unavailable
ea0031cmw3.2
Is there a place for metformin in pcos
ea0031cmw3.3
Diagnosis and management of hirsutism
ea0031cmw3.4
Managing Hypoglycaemia
Hypoglycaemia in diabetes: effects on cerebral and autonomic function
ea0031cmw4.1
Abstract unavailable
ea0031cmw4.2
Hypoglycaemia in neonates and Children
ea0031cmw4.3
Autoimmune hypoglycaemia [ndash] when and how to look for anti-insulin and anti-insulin receptor antibodies
ea0031cmw4.4
Applied Physiology Workshop
Digital copies: exploiting numerical models of biological systems
Modelling neuroendocrine systems
ea0031apw1.1
Distinguishing normal, depressive and PTSD cortisol dynamics in humans through mathematical modelling
ea0031apw1.2
Abstract unavailable
ea0031apw1.3
Modelling the circulating renin[ndash]angiotensin system and its effects on blood pressure
ea0031apw1.4
Debate
(1)
Clinical Debate: this house believes that radio iodine should be the first line treatment for all patients with Graves' disease: FOR
ea0031d1
Against
ea0031d2
Meet the Expert Sessions
(1)
Abstract unavailable
ea0031mte1
Abstract unavailable
ea0031mte2
Abstract unavailable
ea0031mte3
Abstract unavailable
ea0031mte4
Abstract unavailable
ea0031mte5
Malignant phaeochromocytomas
ea0031mte6
Hormone misuse in sport and leisure
ea0031mte7
Nanometre-resolution imaging of hormonal secretion in living cells in real time
ea0031mte8
Abstract unavailable
ea0031mte9
Nurse Session
The Patient Pathway for Pituitary Care
Abstract unavailable
ea0031n1.1
Abstract unavailable
ea0031n1.2
Abstract unavailable
ea0031n1.3
Abstract unavailable
ea0031n1.4
Abstract unavailable
ea0031n1.5
Late Effects
Abstract unavailable
ea0031n2.1
Abstract unavailable
ea0031n2.2
Gonadal late effects
ea0031n2.3
Young Endocrinologists Session
Young endocrinologists' prize lectures
Clinical and pre-clinical studies of neuroendocrine tumours (NETs) in multiple endocrine neoplasia type 1 (MEN1), and evaluation of MEN1 gene replacement therapy for MEN1-associated NETs.
ea0031yep1.1
The Wnt/[beta]-catenin effector Tcf3/TCF7L1 is required for normal hypothalamic[ndash]pituitary development
ea0031yep1.2
Maintaining your endocrine career despite what life throws at you
Maintaining an active basic research career whilst juggling an academic and personal life
ea0031ye1.1
Juggling a clinical workload: and academic research
ea0031ye1.2
Abstract unavailable
ea0031ye1.3
Non-traditional career paths towards an academic career
ea0031ye1.4
Daphne Jackson Fellowships offer returners the chance to re-establish a research profile after a career break
ea0031ye1.5
Abstract unavailable
ea0031ye1.6
Senior Endocrinologists Session
(1)
Robert Graves' and his remarkable colleagues
ea0031se1.2
Robert Graves' and his remarkable colleagues
ea0031se1.2 (1)
Should the aging male become a father?
ea0031se1.3
Hypovitaminosis-D and the RAS in type 2 diabetes risk
ea0031se1.4
Type 1 and type 2 diabetes are the same disorder of insulin resistance, but with different genetic backgrounds
ea0031se1.5
Suspicious hypoglycaemia; was it insulin?
ea0031se1.6
Oral Communications
Young Endocrinologists prize session
TNF[alpha] directly regulates in vivo corticosteroid metabolism in inflammatory arthritis
ea0031oc1.1
Macrophage-specific 11[beta]-hydroxysteroid dehydrogenase type 1 deficiency promotes angiogenesis but impairs resolution of K/BxN serum induced arthritis
ea0031oc1.2
11[beta]-HSD1KO mice are protected from glucocorticoid dependent age-associated muscle atrophy
ea0031oc1.3
A serum microRNA profile potentially associated with glucocorticoid mediated insulin resistance
ea0031oc1.4
Inhibition of 5[alpha]-reductase type 1 with dutasteride impairs insulin sensitivity
ea0031oc1.5
Improving the vitamin D status of vitamin D deficient adults is associated with improved mitochondrial oxidative function in skeletal muscle
ea0031oc1.6
Autosomal dominant hypocalcemia type 2 is caused by germline GNA11 gain-of-function mutations
ea0031oc1.7
Kisspeptin advances ovulation in healthy women
ea0031oc1.8
Steroids and thyroid
Loss-of-function mutations in IGSF1 cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement
ea0031oc2.1
Abnormal cardiac bio-energetics in subclinical hypothyroidism; cardiac magnetic resonance spectroscopic study
ea0031oc2.2
A bi-transgenic murine model of PTTG and PBF overexpression in the thyroid gland
ea0031oc2.3
THRA or DIO2 mutations are not a common cause of high bone mass in humans
ea0031oc2.4
A mutation in thioredoxin reductase 2 (TXNRD2) is associated with a predominantly adrenal phenotype in humans
ea0031oc2.5
An N-ethyl-N-nitrosourea induced Corticotrophin releasing hormone promoter mutation provides a mouse model of Cushing's syndrome
ea0031oc2.6
11β-hydroxysteroid dehydrogenase type 1: a role in skin wound healing
ea0031oc2.7
When math meets biology: systems approach to drug resistance analysis
ea0031oc2.8
Reproduction, growth and development
Identification of very early sorting endosomes that spatially program gonadotrophin hormone receptor signalling
ea0031oc3.1
Heterodimerisation of GNRH receptors modifies the LH-induced calcium signalling profile
ea0031oc3.2
Regulation of G protein-coupling specificity via cis and trans activation of the LH/chorionic gonadotrophin receptor (LHCGR)
ea0031oc3.3
Characterising changes in the in vivo male rodent brain using magnetic resonance spectroscopy
ea0031oc3.4
Effects of in utero exposure to acetaminophen (paracetamol) on steroidogenesis by the rat and human fetal testis
ea0031oc3.5
Follistatin-like 3 (FSTL3), a transforming growth factor β ligand inhibitor, is essential for placental development in mice
ea0031oc3.6
Disruption of mesenchymal glucocorticoid signaling attenuates embryonic lung development and results in post natal lethality in mice
ea0031oc3.7
Adiponectin induces GSK3 kinase-mediated cross-tolerance to endotoxin in macrophages
ea0031oc3.8
Obesity, metabolism and bone
Glucocorticoid receptor deficiency in cardiomyocytes causes pathological cardiac remodelling in mice
ea0031oc4.1
11[beta]-HSD1 knockout mice are protected from the adverse metabolic effects of exogenous glucocorticoid excess
ea0031oc4.2
Adult offspring of undernourished sheep exhibit epigenetic alterations in HPA axis glucocorticoid receptor
ea0031oc4.3
Cholestatic pregnancy programmes metabolic disease in the offspring
ea0031oc4.4
Energy intake following infusion of glucagon and GLP-1: a double-blind crossover study
ea0031oc4.5
Transgenic disruption of 5α-reductase 1 increases susceptibility to liver fibrosis
ea0031oc4.6
Familial hypocalciuric hypercalcaemia type 3 is caused by mutations in adaptor protein 2 sigma 1
ea0031oc4.7
Peptide YY regulates bone mineral content and strength
ea0031oc4.8
Pituitary and neoplasia
Genetic background influences tumour phenotype in heterozygous Men1 knockout mice
ea0031oc5.1
The role of microRNA miR-34a in the regulation of aryl hydrocarbon receptor interacting protein
ea0031oc5.2
Whole-exome sequencing studies of non-functioning pituitary adenomas
ea0031oc5.3
Clinical, metabolic, biochemical and radiological characterisation of patients with thyrotropinomas reveals a highly variable phenotype
ea0031oc5.4
Densely and sparsely granulated somatotroph adenomas: clinical, genetic and histological differences
ea0031oc5.5
Manipulating PBF/PTTG1IP phosphorylation status to improve radioiodine uptake in thyroid and other tumours
ea0031oc5.6
Uterine tumours with loss of progesterone receptor expression develop in mice deleted for a cell division cycle 73 allele
ea0031oc5.7
Pituitary adenoma and phaeochromocytoma/paraganglioma [ndash] a novel syndrome with a heterogeneous genetic background
ea0031oc5.8
Poster Presentations
Bone
GNA11 loss-of-function mutations cause familial hypocalciuric hypercalcaemia type 2 (FHH2)
ea0031p1
Increased linear bone growth in SOCS2 knockout mice in response to GH is independent of systemic or local IGF1
ea0031p2
Mutations in CLC-5 cause disturbances in cytoskeletal dynamics and solute transport in Dent's disease renal proximal tubule cell-lines
ea0031p3
Contribution to bone mass and strength of osteoblast GH actions that are independent of local IGF1 production: lessons from the SOCS2 knockout mouse
ea0031p4
Mimicking osteocytes
in vivo
using 3D collagen gels: development of a novel tool to study osteocyte biology
ea0031p5
Retinoic acid and IGF1 stimulate the differentiation of human primary osteoblasts to osteocytes in 3D collagen gels
ea0031p6
Alterations of CLC-5 expression, function and trafficking in Dent's disease
ea0031p7
Excessive GH expression in bGH transgenic mice adversely alters bone architecture and quality
ea0031p8
Bone health in type 1 diabetes patients with celiac disease
ea0031p9
High throughput detection of early joint pathology in mouse models of osteoarthritis
ea0031p10
Bone health in children with GH deficiency
ea0031p11
Vitamin D receptor polymorphisms and bone mass indices in post menarcheal Indian adolescent girls
ea0031p12
Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene manifesting clinically as osteogenesis imperfecta
ea0031p13
Bone mass accrual following supplementation of vitamin D alone versus vitamin D+ calcium in underprivileged Indian premenarcheal girls
ea0031p14
Primary hyperparathyroidism in patients with urolithiasis: prevalence and predictors
ea0031p15
Impact of hyponatraemia in patients with fracture neck of femur
ea0031p16
Risperidone associated changes in prolactin and bone mineral density: a study from South India
ea0031p17
Predictors of low bone mineral density in an Irish cystic fibrosis (CF) cohort
ea0031p18
Comparison of different measures of urinary calcium excretion in primary hyperparathyroidism
ea0031p19
Metabolic sydrome in women with osteoporosis on bisphosphonate therapy
ea0031p20
The utility of neck MRI in the localisation of parathyroid adenomas in primary hyperparathyroidism
ea0031p21
Renal replacement therapy to treat severe hypercalcaemic crisis: case series
ea0031p22
Audit of cost-saving following introduction of investigation protocol for primary hyperparathyroidism
ea0031p23
Effect of bone mineral density in patients with non-functioning pituitary adenoma
ea0031p24
Proximal myopathy: a diagnostic dilemma
ea0031p25
Audit of primary hyperparathyroidism management: do we adhere to the guidelines?
ea0031p26
The diagnosis of osteoporosis among subjects of Southern Indian origin above 50 years of age: the impact of the indian council of medical research vs caucasian bone mineral density reference standards
ea0031p27
Not the end of brown tumours: three cases within 12 months
ea0031p28
A case of severe immobilization hypercacemia in a young patient on neurorehabilitation unit
ea0031p29
Cinacalcet treatment for hypercalcaemia in primary hyperparathyroidism
ea0031p30
AUDIT of patients referred for DXA scanning in a south Indian Tertiary care centre
ea0031p31
Audit of management of patients with primary hyperparathyroidism in district general hospital
ea0031p32
Osteogenic malignancy and severe vitamin D deficiency (osteogenic osteomalacia)
ea0031p33
Osteogenic malignancy and severe vitamin D deficiency (Osteogenic osteomalacia)
ea0031p34
Clinical biochemistry
A rapid and sensitive LC-MS/MS assay for the routine analysis of estradiol and estrone
ea0031p35
The search for 3-Epi-25-hydroxy vitamin D
ea0031p36
Plasma metanephrine analysis by online solid phase extraction LC-MS/MS
ea0031p37
Development of an inductively coupled plasma-mass spectrometry method for measurement of urine iodine and assessment of iodine status in subclinical hypothyroidism
ea0031p38
Cross-reactivity of ten recombinant insulin preparations in the Abbott Architect Insulin immunoassay
ea0031p39
HPLC analysis on separation of BSA from dilute solution
ea0031p40
MSIA-SRM assay for parathyroid hormone and vitamin D binding protein: correlation with clinical immunoassay methods and application to clinical samples
ea0031p41
Glycosylated linkers to generate long-acting GH tandems
ea0031p42
High pulmonary artery pressure is associated with BNP and NT-proBNP in lowlanders acclimatising to high altitude
ea0031p43
Danazol cross-reacts in the Roche E170 testosterone assay
ea0031p44
Persistent hyperparathyroidism following parathyroidectomy: can routine vitamin D replacement prior to surgery alter post-operative secondary hyperparathyroidism?
ea0031p45
Service review and demand management following clinical audit of urine free cortisol requesting at Barts Health NHS Trust
ea0031p46
Hyponatremia in patients with fractured neck of femur: short and medium term outcomes
ea0031p47
A comparison of serum chromogranin A measurement with 24 h urine and serum 5-hydroxyindole acetic acid measurement in patients with NETs
ea0031p48
An unusual case of chronic liquorice ingestion presenting as hypokalemic paralysis
ea0031p49
Role of urinary dopamine in investigation of phaeochromocytoma/paraganglioma
ea0031p50
Liquorice induced hypertension and hypokalaemia
ea0031p51
Calcification of basal ganglia in chronic hypoparathyroidism
ea0031p52
A review of causes of hypomagnesaemia in hospital patients and its management
ea0031p53
An audit on management of hyponatraemia in hospitalised patients
ea0031p54
Impact of hyponatraemia in critically ill patients
ea0031p55
Audit of inpatient management of hyponatraemia
ea0031p56
Clinical practice/governance and case reports
Initiation and maintenance of mitotane as adjuvant therapy for adrenocortical cancer: a single centre experience
ea0031p57
De Novo HNF1b mutation as a cause for chronic treatment-resistant hypomagnesaemia
ea0031p58
Outcomes of transsphenoidal surgery (TSS) for acromegaly
ea0031p59
How do medical students and doctors learn clinical endocrinology?
ea0031p60
An unusual cause of Cushing's syndrome with secondary adrenal insufficiency
ea0031p61
Management of intercurrent illness in adrenal insufficiency
ea0031p62
A case of Hashimoto's thyroiditis induced coagulopathy
ea0031p63
Conn's syndrome with normal plasma renin aldosterone ratio
ea0031p64
Peri-operative [alpha]-blockade: efficacy of intravenous phenoxybenzamine vs oral phenoxybenzamine in patients with phaeochromocytoma and paraganglioma
ea0031p65
A very interesting presentation: VIP co-secretion by a phaeochromocytoma
ea0031p66
A single pathology specialty service for hyperthyroid patients improves care and outcomes compared to general endocrine clinics: results and implications of an audit: re-audit cycle of clinical outcomes for differing hyperthyroid care models
ea0031p67
Novel use of subcutaneous octreotide via an insulin pump for postural orthostatic tachycardia syndrome
ea0031p68
Management of primary hyperparathyroidism during pregnancy: a case series of the lessons learnt
ea0031p69
Normal plasma and urine catecholamines in a patient with symptoms and radiological findings of a phaeochromocytoma cured by laparoscopic adrenalectomy
ea0031p70
Bariatric surgery in a patient with melanocortin 4 receptor mutation
ea0031p71
Tolvaptan treatment in hyponatraemia due to chronic heart failure
ea0031p72
Hypercalcaemia secondary to colecalcifrol administration in undiagnosed sarcoidosis
ea0031p73
Spironolactone interference in the immunoassay of androstenedione in a patient with a cortisol-secreting adrenal adenoma
ea0031p74
An unusual case of confusion and hyponatraemia
ea0031p75
Hypernatraemia with reset osmostat associated with secondary hypogonadism
ea0031p76
A case of dry beriberi following bariatric surgery
ea0031p77
Giant parathyroid adenoma extending into the mediastinum: a case report
ea0031p78
Tertiary hyperparathyroidism due to chronic severe vitamin D deficiency in ethnic minority patients: a case series
ea0031p79
Hypercalcaemia due to simultaneous presentation of primary hyperparathyroidism and metastatic oesophageal cancer
ea0031p80
'There is nothing more deceptive than an obvious fact', Sherlock Holmes: a case report of thyroid sarcoidosis
ea0031p81
A case of severe hypoaldosteronism following unilateral adrenalectomy for Conn's syndrome
ea0031p82
SDHB mutation and a large asymptomatic paraganglioma in a young woman: the importance of taking a good family history
ea0031p83
The challenges of a dopamine secreting paraganglioma
ea0031p84
Lithium-induced hyperparathyroidism successfully treated with cinacalcet: two case reports
ea0031p85
Recurrence of a brown tumour in a patient with secondary hyperparathyroidism due to severe vitamin D deficiency
ea0031p86
An uncommon presentation of a common endocrine condition
ea0031p87
Rare case of pheochromocytoma presenting in pregnancy
ea0031p88
Non islet cell tumour hypoglycaemia resistant to medical treatment
ea0031p89
An unusual case of pancreatitis: a case report
ea0031p90
A painful neck in a young well looking man presenting to A[amp]E
ea0031p91
Life threatening airway obstruction secondary to a large probable parathyroid cyst
ea0031p92
Tuberous sclerosis: an uncommon cause of hyperprolactinemia
ea0031p93
Acute diabetic autonomic neuropathy as phaeochromocytoma mimic
ea0031p94
Hypervitaminosis D, an uncommon reality!
ea0031p95
Simultaneous presentation of Graves[apos] thyrotoxicosis and Addison[apos]s disease presenting as incipient adrenal crisis
ea0031p96
Severe refractory non-islet cell tumour hypoglycaemia due to metastatic colorectal carcinoma
ea0031p97
Unusual presentation of central pontine myelinolysis
ea0031p98
SIADH and bilateral adrenal infarction in a patient with the antiphospholipid syndrome
ea0031p99
Incidental papillary thyroid carcinoma with primary hyperparathyroidism: two cases
ea0031p100
Hypercalcaemia as first presentation of sarcoidosis
ea0031p101
Tumours metastatic to the pituitary gland presenting with atypical symptoms
ea0031p102
Acute adrenal insufficiency due to bilateral adrenal haemorrhagic infarction associated with sepsis secondary to an open fracture of the ankle
ea0031p103
Ectopic thyroid tissue presenting as metastatic follicular cancer
ea0031p104
A peculiar case of a dog bite
ea0031p105
Management of diabetic ketoacidosis in a district general hospital: a 3 years retrospective audit
ea0031p106
Unusual presentations of adrenocortical tumours
ea0031p107
An audit of the diagnosis and management of hypogonadism in adult men
ea0031p108
Pituitary tuberculosis
ea0031p109
The difficulties in diagnosing and treating phaeochromocytoma in a patient with multiple co-morbidities
ea0031p110
Adrenal incidentalomas: who requires further testing?
ea0031p111
GH therapy in adults with Prader[ndash]Willi syndrome
ea0031p112
Primary hyperparathyroidism in pregnancy: a conservative approach
ea0031p113
Audit of the management of primary hyperparathyroidism at Watford general hospital
ea0031p114
Potential role of antituberculosis treatment as cause of severe hypocalcaemia immediately following total thyroidectomy
ea0031p115
Pelvic pain in a type 2 diabetes patient
ea0031p116
Clinical practice hyperaldosteronism: a misleading adrenal tumor
ea0031p117
Bilateral adrenal calcification caused by a previous Streptococus mitis septicaemia
ea0031p118
A question of GH deficiency or not
ea0031p119
Ectopic ACTH syndrome as a presenting symptom of bronchogenic carcinoma
ea0031p120
Secondary diabetes due to phaeochromocytoma
ea0031p121
Absent thyroid with GH deficiency
ea0031p122
Degree of bone mineral density improvement in patients with osteoporosis on current NICE recommended treatments: an audit
ea0031p123
Accelerated renal impairment in a patient with type 2 diabetes with an inadequately investigated incidental adrenal adenoma
ea0031p124
Nephrogenic diabetes insipidus caused by lithium toxicity
ea0031p125
Title: A case of primary hypoadrenalism secondary to amyloidosis
ea0031p126
A challenging case of recurrent disabling severe hypoglycemic episodes
ea0031p127
'Gastroparesis' in a patient with uncontrolled diabetes: NOT always autonomic neuropathy!
ea0031p128
Audit on continuous subcutaneous insulin infusion
ea0031p129
Radioactive iodine-induced hyperparathyroidism
ea0031p130
A case of phaeochromocytoma presenting as incidentloma
ea0031p131
Propylthiouracil-induced severe agranulocytosis!
ea0031p132
Rare onset of polyendocrinopathies in a pediatric patient
ea0031p133
Diarrhoea and an adrenal incidentaloma
ea0031p134
Multiple autoimmune diseases: is it rare?
ea0031p135
Cytokines and growth factors
Effect of acute hypoxia upon myostatin expression in healthy individuals
ea0031p136
Genes for IGF2 and related IGF binding proteins are associated with longitudinal trends in BMI
ea0031p137
Comparing the effect of rimonabant and metformin on vascular endothelial growth factor levels in women with PCOS
ea0031p138
IGF binding protein-2 is associated with all-cause and cardiovascular mortality in type 2 diabetes
ea0031p139
Growth and development
Comprehensive spatio-temporal expression profiling reveals a complete natriuretic peptide system in the developing Zebrafish (Danio rerio)
ea0031p140
Impaired heart function and cardiac maturation in fetal mice with disrupted GR signalling in vascular smooth muscle and cardiomyocytes
ea0031p141
Impact of a low protein diet during pregnancy in sheep on insulin and vascular endothelial growth factor signalling
ea0031p142
Reduced glucocorticoid action in obese pregnancy associates with increased birth weight and macrosomia
ea0031p143
Identification of twenty-two novel GATA3 mutations in hypoparathyroidism-deafness-renal dysplasia syndrome
ea0031p144
Familial constitutional delay in growth and puberty is a condition with significant genetic heterogeneity and limited overlap with the timing of puberty in the general population
ea0031p145
Pre-clinical investigation of therapy for segmental overgrowth caused by constitutive activation of phosphoinositide-3 kinas: lessons for cancer therapy
ea0031p146
Effects of the endocrine disrupting herbicide, Atrazine, on pituitary development, gene expression and signalling pathways in Zebrafish (Danio rerio) and mouse pituitary cell lines
ea0031p147
The spectrum of associated congenital anomalies in disorders of sex development: a review of the I-DSD Registry
ea0031p148
Neoplasia, cancer and late effects
Epigenetic modifiers reduce proliferation of human neuroendocrine tumour cell lines
ea0031p149
POMC correlates with viable tumour cell mass in lung cancer xenografts
ea0031p150
Phenotype[ndash]genotype analysis in a cohort of patients with multiple endocrine neoplasia type 1 identifies a novel nonsense mutation at codon 554
ea0031p151
Parathyroid gland studies in mouse models for endocrine tumours defines anatomical locations and ultrastructural differences between normal and tumour cells
ea0031p152
Functional induction of the oestrogen-regulated PTTG1-binding factor in colorectal cancer
ea0031p153
PBF overexpression causes increased p53 ubiquitination and degradation via MDM2
ea0031p154
Mechanisms of estrogen receptor function in breast cancer
ea0031p155
Investigation of the antiproliferative effect of natural sesquiterpene lactones on human cancer cell lines
ea0031p156
Predicted NES in PBF appears to be functional in vitro
ea0031p157
Pituitary metasases: patients presenting with cranial nerve palsies and diabetes insipidus: a single centre experience
ea0031p158
The relationship between anatomical location of phaeochromocytoma and paraganglioma and their secretory properties
ea0031p159
Adjuvant use of 131I-MIBG in phaeochromocytoma and paraganglioma at high risk of malignancy
ea0031p160
Multi-modal approach to treatment in advanced adrenocortical carcinoma
ea0031p161
Prevalence of multiple endocrine neoplasia type 1 syndrome in primary hyperparathyroidism
ea0031p162
Primary thyroid cancer as late effects of childhood cancer therapy: a case series of five patients
ea0031p163
Diagnosis, localisation and management of insulinoma; a single-centre experience
ea0031p164
Audit of patients with multiple endocrine neoplasia type 1 in a tertiary referral centre
ea0031p165
Difficulties in management of malignant insulinoma
ea0031p166
Crizotinib induced hypogonadism: a novel complication of lung cancer treatment
ea0031p167
Review of patients with adrenocortical carcinoma at a tertiary referral centre
ea0031p168
Between genetics, guidelines and treatment in MEN2A: a family affair
ea0031p169
Cowden syndrome
ea0031p170
Recurrent bronchial carcinoid tumour presenting as a thyroid nodule
ea0031p171
Gut carcinoid in a patient with horseshoe kidney and family history of carcinoid syndrome: a case report
ea0031p172
Insulinoma in postprandial hypoglycaemia and aggressive behaviour
ea0031p173
Hyperparathyroid jaw tumour syndrome
ea0031p174
Nursing practice
Using a nursing model in the management of a patient with McCune[ndash]Albright syndrome
ea0031p175
Development of adult endocrine specialist nurse competencies
ea0031p176
Obesity, diabetes, metabolism and cardiovascular
Association of calcium-sensing receptor polymorphisms with vascular calcification and glucose homeostasis in renal transplant recipients
ea0031p177
Testosterone stimulates cholesterol efflux and metabolism in human macrophages via liver X receptor
ea0031p178
FGF21 action on human adipose tissue compromised by reduced [beta]Klotho and FGFR1 expression in type 2 diabetes mellitus
ea0031p179
A component of transcriptional PRC2 complex, enhancer of zest homology, modulates endothelial cell responses to hypoxia and post-ischemic angiogenesis in a mouse model of limb ischemia
ea0031p180
The role of hepatic 11[beta]-hydroxysteroid dehydrogenase type 1 in cholesterol homeostasis
ea0031p181
Vitamin B12 and folate imbalance induces cholesterol synthesis and endoplasmic reticulum stress in human adipocytes
ea0031p182
The effects of Syzygium aromaticum-derived oleanolic acid on reactive oxygen species in the heart, liver and kidney of STZ-induced diabetic rats
ea0031p183
Effects of vitamin D supplementation on blood pressure, glucocorticoids and cardiovascular risk markers in healthy subjects
ea0031p184
Knockdown of brain 11[beta]-HSD1 does not lower body weight or improve insulin sensitivity
ea0031p185
C-type natriuretic peptide down regulates interferon [gamma] mediated pro-inflammatory gene expression in human endothelium
ea0031p186
Acute effects of co-infusion of peptide YY (3[ndash]36) and glucagon-like peptide-1 on insulin secretion and insulin sensitivity
ea0031p187
Human abdominal subcutaneous adipocytes as an active source of LpPLA2, influenced by fat depot and metabolic state, with LpPLA2 converting LDL into more potent atherogenic Ox-LDL, in vitro
ea0031p188
The role of glucocorticoid metabolism in bile acid homeostasis
ea0031p189
Testosterone differentially regulates lipid and glucose metabolism in visceral and subcutaneous fat in the testicular feminised mouse
ea0031p190
Novel inositol pyrophosphate and insulin sensitivity in response to muscle contraction in glucose intolerant humans
ea0031p191
Augurin stimulates food intake in male Wistar rats
ea0031p192
Abstract unavailable
ea0031p193
Intracellular delivery of therapeutic siRNA via an antennapedia-double stranded RNA binding domain fusion protein as a novel strategy for PTP1B translation attenuation in type 2 diabetes
ea0031p194
Replication of genome wide association-validated loci for type 2 diabetes mellitus in the Saudi Arabian population
ea0031p195
Cellular consequences for insulin signal transduction of the naturally occurring AKT2 p.Glu17Lys mutation
ea0031p196
DPPIV and macronutrients regulate the expression of PYY3[ndash]36 in human gut epithelial cells
ea0031p197
Inflammatory markers in diabetic foot and impact of vitamin D deficiency
ea0031p198
The possible involvement of the receptor for advanced glycation end products in vascular senescence in diabetes
ea0031p199
Effects of Syzygium aromaticum-derived oleanolic acid administration on postprandial glucose concentration and key intestinal carbohydrate hydrolyzing enzymes of streptozotocin-induced diabetic rats
ea0031p200
Unfolded protein response pathway, IRE1[alpha]-XBP1 is altered during adipogenesis in obese human adipocytes
ea0031p201
Vitamin D and insulin resistance: no association in healthy overweight people at high risk of cardiovascular disease
ea0031p202
Evaluation of efficacy of transdermal delivery of chloroquine on Plasmodium berghei-infected male Sprague[ndash]Dawley rats and effects on blood glucose and renal electrolyte handling
ea0031p203
Altered mitochondrial dynamics in obesity: redressing the balance through bariatric surgery?
ea0031p204
Irisin as a central regulator in energy homeostasis?
ea0031p205
Ileal interposition with diverted sleeve gastrectomy for treatment of type 2 diabetes
ea0031p206
Polycystic ovary syndrome has no independent effect on vascular, inflammatory or thrombotic markers when matched for obesity
ea0031p207
Leptin in serum and vitreous humor, and retinal ob mRNA, in human diabetes
ea0031p208
The endocrine and metabolic characteristics of a large Bardet[ndash]Biedl syndrome clinic population
ea0031p209
Maternal B12 insufficiency predicts neonate's metabolic risk factors
ea0031p210
The use of GLP-1 receptor agonists to manage unwanted weight gain in patients with 'hypothalamic' obesity secondary to structural pituitary pathology
ea0031p211
The public distress domain of quality of life correlates directly and independently with BMI in pre-operative morbidly obese patients awaiting metabolic surgery
ea0031p212
Pregestational BMI predicts neonatal hypoglycemia in women with gestational diabetes
ea0031p213
Effectiveness of bariatric surgery in women with and without polycystic ovarian syndrome
ea0031p214
Octreotide therapy of chronic urticaria and angioedema after gastric bypass procedure
ea0031p215
Prevalence of vitamin D insufficiency in severely obese patients seeking bariatric surgery
ea0031p216
Appetite regulation during a 6-month military tour to Afghanistan
ea0031p217
Weight loss after bariatric surgery in women of childbearing age
ea0031p218
Eating more quickly heightens overall systemic exposure to glucose and NEFA in the post-prandial phase, irrespective of energy expenditure in obese women
ea0031p219
Hepatic 11[beta]-hydroxysteroid dehydrogenase type 1 is elevated following weight loss secondary to bariatric surgery
ea0031p220
Brown adipose tissue identification in an adult human using IDEAL MRI
ea0031p221
Vitamin D supplementation as influenced by diabetic therapies
ea0031p222
Association of the incidence of type 1 diabetes with markers of infection and antibiotic susceptibility at country level
ea0031p223
A pilot study of 25-hydroxy vitamin D level in type 2 diabetes mellitus with diabetic retinopathy
ea0031p224
Non-alcoholic fatty liver disease in patients attending the National Severe Insulin Resistance Service
ea0031p225
A study of serum osteocalcin level in women with gestational diabetes mellitus
ea0031p226
Short term calorie restriction: effects on endocrine markers of nutritional status
ea0031p227
The development of a structured education programme to improve cardiovascular risk in women with polycystic ovary syndrome (SUCCESS Study)
ea0031p228
Hypogonadism in males with type 2 diabetes mellitus
ea0031p229
Obesity-related hypogonadotrophic hypogonadism: recovery of normal pituitary[ndash]gonadal axis function following bariatric surgery
ea0031p230
Risk assessment of adult residents in ile-ife, South-Western Nigeria for type 2 diabetes mellitus
ea0031p231
Adrenal insufficiency post bariatric surgery
ea0031p232
Pregnancy outcome in a patient with lipodystrophy and type 2 diabetes
ea0031p233
Impaired iron status in severely obese bariatric surgery candidates is multifactorial
ea0031p234
What lies beneath: a case of spontaneous hypoglycaemia or glucose transporter type 1 defect disguised as chronic fatigue?
ea0031p235
Improvement in testosterone post bariatric surgery
ea0031p236
Prevalence and associated risks for metabolic syndrome in nigerians with type 2 diabetes mellitus
ea0031p237
Ethnic specific anthropometric values have been used by the International Diabetes Federation to aid in the diagnosis of the metabolic syndrome: no such values are available for Sub-Saharan Africa including Nigeria
ea0031p238
Preoperative characteristics of morbidly obese patients who achieved at least 50% excess weight loss post-metabolic Surgery
ea0031p239
Glycaemic variability: does it make a difference in prediabetes?
ea0031p240
Unusual case of hypoglycaemia in diabetic patient
ea0031p241
withdrawing insulin in a young person
ea0031p242
Re-occurrence of pancreatic insulinoma: an usual cause of hypoglycaemia
ea0031p243
Pituitary
Secretory granule accumulation in anterior pituitary somatotrophs of TPC1 null mice
ea0031p244
Transport features of pituitary folliculostellate cells increase in pregnancy
ea0031p245
Chronic glucocorticoid exposure causes de-novo methylation of genes key to the regulation of the hypothalamic[ndash]pituitary[ndash]adrenal axis
ea0031p246
Polymersomes-mediated siRNA delivery for states of hormone excess
ea0031p247
Transcriptional regulation of C-type natriuretic peptide (CNP/Nppc) and its receptor guanylyl cyclase-B (GC-B/Npr2) in gonadotroph and somatolactotroph cell lines
ea0031p248
'Invasion signature' revealed by the analysis of AIP positive and AIP mutation negative human pituitary adenomas
ea0031p249
Maternal vocalisation as an effective priming method for oxytocin in young adults
ea0031p250
Altitude acclimatization: plasma AVP response and physiological changes
ea0031p251
Craniopharyngiomas and Wnt signalling pathways
ea0031p252
In vivo characterisation of skeletal muscle metabolism in GH deficient adults using phosphorus-31 magnetic resonance spectroscopy
ea0031p253
Creation of a locus-specific database for AIP mutations
ea0031p254
High prevalence of pituitary dysfunction following blast traumatic brain injury: results from the UK Blast Injury Outcome Study of Armed Forces Personnel (BIOSAP)
ea0031p255
Correlation of clinical smell test and magnetic resonance imaging of olfactory system in idiopathig hypogonadotropic hypogonadism
ea0031p256
Endocrine remission of Cushing's disease after endoscopic trans-sphenoidal surgery: Retrospective review of a single centre experience
ea0031p257
Prevalence of familial isolated pituitary adenomas
ea0031p258
Short-term (3 months) compared to long-term response to somatostatin analogues in acromegaly
ea0031p259
Incidental pituitary haemorrhage is common in prolactin-secreting macroadenoma especially in women
ea0031p260
Ophtalmological, endocrine, and neurological complications in giant male prolactinomas.
ea0031p261
Endocrine and radiological abnormalities in empty sella syndrome
ea0031p262
11C-methionine PET[ndash]CT co-registered with volume MRI identifies residual functioning tumour in acromegaly
ea0031p263
A retrospective cohort study of patients with hyperprolactinaemia
ea0031p264
Examining the distribution of abdominal fat in GH deficiency using magnetic resonance imaging
ea0031p265
Long-term results after treatment of craniopharyngioma: experience with 46 adult patients
ea0031p266
Syndrome of inappropriate antidiuretic hormone secretion and treatment with tolvaptan: a case series
ea0031p267
Hyponatraemia assessment and outcomes in acute medically ill patients
ea0031p268
Inside acromegaly: a pilot study for recruiting focus groups using social media
ea0031p269
Pituitary apoplexy: a case series
ea0031p270
An unusual cause of testosterone deficiency
ea0031p271
Rare case of round blue cell pituitary tumour with probable hypothalamic involvement
ea0031p272
Pituitary abscess: a rare cause of pituitary mass lesion
ea0031p273
Hypopituitarism presenting with features of stiff person syndrome
ea0031p274
Snake bite and hypopituitarism: ignorance or incompetence?
ea0031p275
TSH-secreting pituitary adenoma identified in pregnancy: management of an unusual case
ea0031p276
A rising TSH in a patient with known TSHoma does not necessarily indicate recurrence
ea0031p277
Unusual presentation of acromegaly and functioning pituitary gonadotrophinoma (FSHoma)
ea0031p278
Pituitary apoplexy and aortic dissection
ea0031p279
Isolated central hypoadrenalism as the sole manifestation of presumed neurosarcoidosis
ea0031p280
Etiology and outcome of hyponatremia due to pituitary insufficiency in a tertiary endocrine center
ea0031p281
Spontaneous resolution of pituitary Cushing's
ea0031p282
A case of complex neurodevelopmental abnormality causing asymptomatic SIADH
ea0031p283
Hypopituitarism with visual field loss is not always an adenoma
ea0031p284
Rapidly progressive pituitary carcinoma in a young female
ea0031p285
Growth of a meningioma in a female patient with uncontrolled congenital adrenal hyperplasia
ea0031p286
Finally we know! 'It comes from your pituitary'
ea0031p287
Inflammatory markers in polycystic ovarian syndrome and their association with cardiovascular risk factors
ea0031p288
Maternal corticosterone regulates amino acid allocation to fetal growth in mice
ea0031p289
BMP4 induces terminal differentiation of primary trophoblast cells and increases chorionic gonadotrophin secretion
ea0031p290
Is diethylstilboestrol an endocrine disruptor in the developing human fetal testis? Effects of DES exposure using a xenograft approach
ea0031p291
Perinatal origins of adult Leydig cells and function: role of developmental androgens
ea0031p292
Pulsatile GnRH signaling to ERK: relevance of pulse duration and frequency
ea0031p293
Intrahepatic cholestasis of pregnancy levels of sulfated progesterone metabolites downregulate hepatic LXR[alpha]
ea0031p294
DNA methyltransferase 3a, 3b and 3L expression in fetal germ cells and its modulation
ea0031p295
Dissecting the prokineticin receptor dimerization interface: a role in kallmann sindrome?
ea0031p296
Tocopherol interacts with [beta]-mimetic effect in reproductive and respiratory tracts in the rat
ea0031p297
Steroid regulation of gene and protein expression of osteopontin and [alpha]v[beta]3 integrin in ovine endometrium
ea0031p298
The effect of mTOR blockers on japanese quail ovarian granulosa cell functions
ea0031p299
KATP channels are involved in the tocolytic effect of [beta]2 agonists in pregnant rat
ea0031p300
Possible role of fetuin-B in the preterm delivery in the rat
ea0031p301
Effect of t-2 toxin and combination of t-2 toxin with resveratrol and mc2183 on ovarian cells of japanese quails
ea0031p302
In vitro effect of 4-nonylphenol and 17[beta]-estradiol on bovine spermatozoa
ea0031p303
Effects of iron on the steroidogenesis of human adrenocarcinoma (nci-h295r) cell line in vitro
ea0031p304
Gaining a better understanding of individual experiences of weight regulation in polycystic ovary syndrome
ea0031p305
Regulation of LH/CG receptor signaling in human endometrium and perturbations in recurrent pregnancy loss
ea0031p306
Kisspeptin-54 administration stimulates LH pulsatility in women with hypothalamic amenorrhoea
ea0031p307
Effect of ethnicity on the clinical presentations of women with polycystic ovary syndrome: a 20-year retrospective cohort study
ea0031p308
A case of persistent Mullerian duct syndrome
ea0031p309
Pubertal induction in males with hypogonadotropic hypogonadism using long-acting intramuscular testosterone undecanoate 1g depot (Nebido)
ea0031p310
White matter changes on magnetic resonance imaging in Klinefelter syndrome
ea0031p311
Metformin treatment of PCOS: St George's Hospital Endocrine Unit Clinical Experience
ea0031p312
Myotonic dystrophy: a rare cause of primary hypogonadism
ea0031p313
Abstract unavailable
ea0031p314
Steroids
11[beta]HSD1 deficiency increases susceptibility to liver fibrosis by activating hepatic stellate cells
ea0031p315
Validation of CYP11B1 and CYP11B2 regulation by microRNA-24
ea0031p316
Molecular mechanisms underlying the anti-inflammatory properties of 5[alpha]-tetrahydrocorticosterone
ea0031p317
Novel loci for familial autoimmune Addison's disease detected by linkage analysis
ea0031p318
Identification of a duplicated P450 side-chain cleavage enzyme (zCyp11a2) defines initiation and maintenance of steroidogenesis in zebrafish
ea0031p319
Glucocorticoids enhance insulin sensitivity in human hepatocytes
ea0031p320
The zebrafish ferredoxin orthologue Fdx1b is essential for the redox regulation of interrenal steroidogenesis in larvae and adult fish
ea0031p321
Steroid profile response to angiotensin II and ACTH in normal volunteer under high and low salt conditions
ea0031p322
Mechanisms of estrogen receptor transcription in breast cancer
ea0031p323
Continuous measurement of free cortisol profiles
ea0031p324
Dual role of TTC5 cofactor in GR-mediated gene expression
ea0031p325
Identification of a novel CYP11B1 isoform in human adrenocortical cells
ea0031p326
The role of anti-ACTH1[ndash]24 antibodies in synacthen-related adverse events
ea0031p327
19F-magnetic resonance spectroscopy as a tool to quantify 11[beta]-hydroxysteroid dehydrogenase activity in vivo
ea0031p328
P450 side-chain cleavage enzyme autoantibodies in canine Addison's disease
ea0031p329
Quantitative analysis of canrenone in plasma by triple quadrupole mass spectrometry
ea0031p330
Quality of life relates to glucocorticoid treatment regimen, adiposity and insulin resistance in adults with congenital adrenal hyperplasia: UK Congenital adrenal Hyperplasia Adult Study Executive (CaHASE)
ea0031p331
Truncal fat distribution is associated with enhanced glucocorticoid excretion, increased 5[alpha]-reductase activity and higher insulin resistance independent of BMI in women with polycystic ovary syndrome
ea0031p332
Revival of adrenal function in established autoimmune Addison's disease
ea0031p333
Range of urinary steroid metabolite ratios in children undergoing investigation for suspected disorder of steroid synthesis
ea0031p334
Gonadotrophic response to operational deployment in Afghanistan
ea0031p335
Reversal of dilated cardiomyopathy in a patient with Cushing's syndrome after a successful adrenalectomy
ea0031p336
Osteoporosis prophylaxis in medical patients taking corticosteroids
ea0031p337
A 'Heavy' price of beauty therapy
ea0031p338
Spot urine cortisol: creatinine ratio: a useful screening test for patients with Cushing's syndrome
ea0031p339
Successful use of subcutaneous infusion of cortisol in an adult case of congentital adrenal hyperplasia
ea0031p340
An audit of adrenal venous sampling at University College Hospital, London
ea0031p341
An online survey on awareness regarding steroid therapy and sick day rules
ea0031p342
Antiphospholipid antibody syndrome: adrenal insufficiency
ea0031p343
Feature of acute mineralocorticoid excess from ACTH secreting bronchial tumour
ea0031p344
Cranial diabetes insipidus in a patient with previously cured pregnancy associated adrenal Cushing's syndrome
ea0031p345
ACTH independent bilateral macronodular adrenal hyperplasia presenting as subclinical Cushing's syndrome
ea0031p346
A case of hypocalcaemia in ectopic ACTH production
ea0031p347
Bilateral enlarging adrenal masses: when can we wait in indeterminate lesions?
ea0031p348
Hypokalaemia: a happy outcome
ea0031p349
An interesting adrenal adenoma: is it just androgen producing or coproducing both androgen and cortisol
ea0031p350
An interesting case of adrenal adenoma
ea0031p351
Thyroid
Local regulation of T3 availability in susceptibility to osteoarthritis
ea0031p352
Low frequency of pendrin autoantibodies detected using a radioligand binding assay in patients with autoimmune thyroid disease
ea0031p353
Interferon induced thyrotoxicosis
ea0031p354
Levothyroxine therapy affects cerebral blood flow and fatigue in subclinical hypothyroidism
ea0031p355
Thyroid incidentaloma incidence and malignant prevalence in F-18-FDG-PET/CT imaging
ea0031p356
Vitamin D status in autoimmune hypothyroidism
ea0031p357
Prevalence of anti-thyroglobulin antibodies, their prognostic significance and impact on patient care in a cohort of patients with differentiated thyroid cancer
ea0031p358
Factors prompting thyroid function testing in hospitalised patients with thyroid dysfunction: analysis of a large hospital database
ea0031p359
Homozygous resistance to thyroid hormone: can cardiac complications be prevented?
ea0031p360
Factors predicting the development of hypothyroidism after radioactive iodine treatment
ea0031p361
Does closer monitoring of thyroid function post radioiodine reduce the severity of hypothyroidism when first detected?
ea0031p362
Interferon-induced thyroid dysfunction: a case series
ea0031p363
Clinical performance of fine-needle aspiration biopsy of thyroid nodules in a tertiary referral centre
ea0031p364
The challenge of managing refractory amiodarone-induced Graves' disease in resistance to thyroid hormone
ea0031p365
A rapidly enlarging neck lump and Horner's sign: lessons from a novel case
ea0031p366
The presence of thyroid peroxidase antibodies in Graves' disease is predictive of disease duration and relapse rates
ea0031p367
Managing Graves' disease: management involving endocrine nurse led service: experience from DGH
ea0031p368
Thyroid nodules, FNA cytology and thyroid cancer in Malta
ea0031p369
False positive pentagastrin stimulation test in a family with medullary thyroid cancer
ea0031p370
Factors affecting choice of definitive therapy in patients with relapsed thyrotoxicosis
ea0031p371
Levothyroxine absorption testing: a 5-day (usual dose) test as an alternative to the 1-day (1000 [mu]g) test
ea0031p372
Four cases of thyroid carcinoma presenting in childhood: 15 years experience in a National Tertiary Referral Centre
ea0031p373
Acute transient thyrotoxicosis following intensity-modulated radiotherapy to the neck
ea0031p374
Evaluation of fine needle aspiration and ultrasound in diagnostic assessment of thyroid nodules
ea0031p375
Thyroid dermopathy: an extreme variant
ea0031p376
Too low, too high: is it the Roux-en-Y? Fluctuating thyroid function post obesity surgery
ea0031p377
Not all raised T4 needed treatment!
ea0031p378
A case of metastatic papillary thyroid carcinoma presenting with pleural, pulmonary and bone metastases
ea0031p379
Raised TSH: a diagnostic conundrum!
ea0031p380
Bilateral thyroid cysts: an important association not to forget?
ea0031p381
An unusual association with autoimmune hypothyroidism
ea0031p382
Case report: when measured free T4 and free T3 may be misleading. Interference with free thyroid hormones measurements on Roche and Siemens platforms
ea0031p383
Management of thyrotoxic crisis in a brittle asthmatic
ea0031p384
Audit of use of radioactive iodine in the treatment of thyrotoxicosis at the Bristol royal infirmary (2008[ndash]2009)
ea0031p385
Successful pregnancy outcomes with thyroxine treatment in euthyroid women with positive thyroid autoantibodies and recurrent miscarriage
ea0031p386
Carbimazole induced cholestatic hepatitis
ea0031p387
Myxedema Coma: an uncommon presentation of a common thyroid problem
ea0031p388