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

Poster Presentations

Investigation of Androgen Receptor Gen Mutation Spectrum in the Turkish Patients with Disorder of Sex Development
  • Hüseyin Onay
  • Samim Özen
  • Tuba Sözen Türk
  • Şükran Darcan
  • Tahir Atik
  • Ahmet Anık
  • Oya Ercan
  • Olcay Evliyaoğlu
  • Gönül Çatlı
  • Filiz Hazan
  • Ayhan Abacı
J Clin Res Pediatr Endocrinol 2017; 9: 23-23
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Original Article

Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development
  • Birsen Şentürk Pilan
  • Burcu Özbaran
  • Didem Çelik
  • Tuğçe Özcan
  • Samim Özen
  • Damla Gökşen
  • İbrahim Ulman
  • Ali Avanoğlu
  • Sibel Tiryaki
  • Hüseyin Onay
  • Özgür Çoğulu
  • Ferda Özkınay
  • Şükran Darcan
J Clin Res Pediatr Endocrinol 2021; 13: 23-33 DOI: 10.4274/jcrpe.galenos.2020.2020.0141 PMID:32938579
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A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations
  • Aslı Derya Kardelen
  • Güven Toksoy
  • Firdevs Baş
  • Zehra Yavaş Abalı
  • Genco Gençay
  • Şükran Poyrazoğlu
  • Rüveyde Bundak
  • Umut Altunoğlu
  • Şahin Avcı
  • Adam Najaflı
  • Oya Uyguner
  • Birsen Karaman
  • Seher Başaran
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2018; 10: 206-215 DOI: 10.4274/jcrpe.0032 PMID:29595516
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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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Case Report

Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene
  • Ayla Güven
  • Seher Polat
J Clin Res Pediatr Endocrinol 2017; 9: 85-90 DOI: 10.4274/jcrpe.3306 PMID:27476613
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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
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Review

Sex Assignment in Conditions Affecting Sex Development
  • Renata Markosyan
  • S. Faisal Ahmed
J Clin Res Pediatr Endocrinol 2017; 9: 106-112 DOI: 10.4274/jcrpe.2017.S009 PMID:29280745
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Latest Update: 13.04.2021
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