ISSN:1308-5727 E-ISSN:1308-5735

Original Article

Clinical and Biochemical Phenotype of Adolescent Males with Gynecomastia
  • Milosz Lorek
  • Dominika Tobolska-Lorek
  • Barbara Kalina-Faska
  • Aleksandra Januszek- Trzciakowska
  • Aneta Gawlik
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2019.2019.0027 PMID:31117335
Abstract

Case Report

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
  • Assimina Galli Tsinopoulou
  • Anastasios Serbis
  • Eleni P. Kotanidou
  • Eleni Litou
  • Vaia Dokousli
  • Konstantina Mouzaki
  • Pavlos Fanis
  • Vassos Neocleous
  • Nicos Skordis
J Clin Res Pediatr Endocrinol 2018; 10: 74-78 DOI: 10.4274/jcrpe.4829 PMID:28739554
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A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect
  • Tülay Güran
  • Gözde Yeşil
  • Ömer Güran
  • Suna Cesur
  • Oktav Bosnalı
  • Ayşenur Celayir
  • Sevilay Topçuoğlu
  • Abdullah Bereket
J Clin Res Pediatr Endocrinol 2012; 4: 151-153 DOI: 10.4274/Jcrpe.685 PMID:22664361
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Letter to Editor

Reply; Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene
  • Olcay Evliyaoğlu
J Clin Res Pediatr Endocrinol 2016; 8: 107-107 DOI: 10.4274/jcrpe.2765
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Original Research

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
  • Erdal Eren
  • Tuba Edgünlü
  • Emre Asut
  • Sevim Karakaş Çelik
J Clin Res Pediatr Endocrinol 2016; 8: 218-223 DOI: 10.4274/jcrpe.2495 PMID:26761946
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Latest Update: 12.09.2019
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