publication venue for
- Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase. 2017
- 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
- Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients.. 170. 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
- Safety of growth hormone replacement in survivors of cancer and intracranial and pituitary tumours: a consensus statement. 2022
- Beta-cell apoptosis in the pathogenesis of human type 2 diabetes mellitus. 2003