European journal of endocrinology Journal

Overview

publication venue for

Circadian Rhythms, Endogenous Glucocorticoids and Skeletal Health. 2026
Metabolic syndrome in childhood, adolescent, and young adult cancer survivors: recommendations for surveillance from the International Late Effects of Childhood Cancer Guideline Harmonization Group.. 192. 2025
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlation.. 192. 2025
Functional magnetic resonance imaging in primary hyperparathyroidism.. 183. 2020
Early diagnosis of gestational diabetes mellitus using circulating microRNAs.. 181. 2019
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.. 172. 2015
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.. 171. 2014
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.. 170. 2014
Surgery for 'asymptomatic' mild primary hyperparathyroidism improves some clinical symptoms postoperatively.. 169. 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.. 168. 2013
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.. 164. 2011
Determinants of IGF1 and GH across the weight spectrum: from anorexia nervosa to obesity.. 163. 2010
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations.. 162. 2010
Relationships between FSH, inhibin B, anti-Mullerian hormone, and testosterone during long-term treatment with the GnRH-agonist histrelin in patients with prostate cancer.. 162. 2009
Hyperinsulinism-hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype-phenotype correlations.. 161. 2009
Elevated basal and post-feed glucagon-like peptide 1 (GLP-1) concentrations in the neonatal period.. 160. 2008
Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation.. 159. 2008
The role of 6-[18F]fluorodopamine positron emission tomography in the localization of adrenal pheochromocytoma associated with von Hippel-Lindau syndrome.. 156. 2007
Evidence that luteinising hormone receptor polymorphisms may contribute to male undermasculinisation.. 147. 2002
The highly malignant phenotype of anaplastic thyroid carcinoma cell lines is recessive.. 143. 2000
Steroid receptor coactivator-3 glutamine repeat polymorphism and the androgen insensitivity syndrome. 2003
Genetic evidence to exclude the androgen receptor-polyglutamine associated coactivator, ARA-24, as a cause of male undermasculinisation. 2001
Policy decisions on endocrine disruptors should be based on science across disciplines: a response to Dietrich et al.. 169. 2013
GLUT1 deficiency and other glucose transporter diseases. 2004

Identity

ISO Abbreviation

Eur J Endocrinol

Linking ISSN

0804-4643

International Standard Serial Number (ISSN)

0804-4643

Electronic International Standard Serial Number (EISSN)

1479-683X