Original Article

Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey
  • Yasemin Denkboy Öngen
  • Erdal Eren
  • Özgecan Demirbaş
  • Elif Sobu
  • Sian Ellard
  • Elisa De Franco
  • Ömer Tarım
J Clin Res Pediatr Endocrinol 2021; 13: 80-87 DOI: 10.4274/jcrpe.galenos.2020.2020.0093 PMID:32820876

Case Report

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign
  • Emine Çamtosun
  • Zeynep Şıklar
  • Serdar Ceylaner
  • Pınar Kocaay
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2017; 9: 163-167 DOI: 10.4274/jcrpe.3839 PMID:28008861

Original Research

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism
  • Ayla Güven
  • Ayşe Nurcan Cebeci
  • Sian Ellard
  • Sarah E. Flanagan
J Clin Res Pediatr Endocrinol 2016; 8: 197-204 DOI: 10.4274/jcrpe.2408 PMID:26758964