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Volume 177 (2017): Issue 2 (Aug 2017)
in
European Journal of Endocrinology
Online ISSN:
1479-683X
Print ISSN:
0804-4643
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Contents
Review
ENDOCRINOLOGY IN PREGNANCY: Pheochromocytoma in pregnancy: case series and review of literature
MANAGEMENT OF ENDOCRINE DISEASE: Arguments for the prolonged use of antithyroid drugs in children with Graves’ disease
MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation
MECHANISMS IN ENDOCRINOLOGY: The multiple facets of GHRH/GH/IGF-I axis: lessons from lifetime, untreated, isolated GH deficiency due to a GHRH receptor gene mutation
Clinical Studies
Plasma methoxytyramine: clinical utility with metanephrines for diagnosis of pheochromocytoma and paraganglioma
The phenotype of
SDHB
germline mutation carriers: a nationwide study
Diabetes insipidus is an unfavorable prognostic factor for response to glucocorticoids in patients with autoimmune hypophysitis
Tamoxifen reduces hepatic VLDL production and GH secretion in women: a possible mechanism for steatosis development
Real-life GH dosing patterns in children with GHD, TS or born SGA: a report from the NordiNet® International Outcome Study
MR spectroscopy of hepatic fat and adiponectin and leptin levels during testosterone therapy in type 2 diabetes: a randomized, double-blinded, placebo-controlled trial
Improving risk estimates for metabolically healthy obesity and mortality using a refined healthy reference group
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase
Genetic defects in pediatric-onset adrenal insufficiency in Japan
Long-acting PEGylated recombinant human growth hormone (Jintrolong) for children with growth hormone deficiency: phase II and phase III multicenter, randomized studies
Prognostic impact of vascular invasion in differentiated thyroid carcinoma: a systematic review and meta-analysis
Muscle strength in patients with acromegaly at diagnosis and during long-term follow-up
Cortisol-related metabolic alterations assessed by mass spectrometry assay in patients with Cushing's syndrome
Quality of compounded hydrocortisone capsules used in the treatment of children
Case Report
PRKAR1A
mutation causing pituitary-dependent Cushing disease in a patient with Carney complex
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Print ISSN:
0804-4643
Online ISSN:
1479-683X
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