Original Article

A novel homozygous CYP19A1 gene mutation: Aromatase deficiency mimicking congenital adrenal hyperplasia in an infant without obvious maternal virilisation
  • Fatma Dursun
  • Serdar Ceylaner
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.0140 PMID:30074481
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
  • Tülay Güran
  • Başak Tezel
  • Fatih Gürbüz
  • Beray Selver Eklioğlu
  • Nihal Hatipoğlu
  • Cengiz Kara
  • Murat Aydın
  • Enver Simşek
  • Filiz Mine Çizmecioğlu
  • Alev Ozon
  • Firdevs Baş
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.0117 PMID:30111524
Birth Sizes of Neonates with Congenital Adrenal Hyperplasia Secondary to 21-Hydroxylase Deficiency
  • Helmuth G. Dörr
  • Theresa Penger
  • Andrea Albrecht
  • Michaela Marx
  • Thomas M.K. Völkl
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.0149 PMID:30178749
Epicardial fat thickness in children with classic congenital adrenal hyperplasia
  • Kotb Abbass Metwalley
  • Hekma Saad Farghaly
  • Abdelrahman Abdelhamid
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.0153 PMID:30282618
Testicular Adrenal Rest Tumors in Patients with Congenital Adrenal Hyperplasia
  • Esra Deniz Papatya Çakır
  • Fatma Şentürk Mutlu
  • Erdal Eren
  • Aliye Özlem Paşa
  • Halil Sağlam
  • Ömer Tarım
J Clin Res Pediatr Endocrinol 2012; 4: 94-100 DOI: 10.4274/jcrpe.563 PMID:22672867
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

Original Research

Ambulatory Blood Pressure and Subclinical Cardiovascular Disease in Patients with Congenital Adrenal Hyperplasia: A Preliminary Report
  • Nesibe Akyürek
  • Mehmet Emre Atabek
  • Beray Selver Eklioğlu
  • Hayrullah Alp
J Clin Res Pediatr Endocrinol 2015; 7: 13-18 DOI: 10.4274/jcrpe.1658 PMID:25800471
CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children
  • Firdevs Baş
  • Hülya Kayserili
  • Feyza Darendeliler
  • Oya Uyguner
  • Hülya Günöz
  • Memnune Yüksel Apak
  • Fatmahan Atalar
  • Rüveyde Bundak
  • Robert C. Wilson
  • Maria I. New
  • Bernd Wollnik
  • Nurçin Saka
J Clin Res Pediatr Endocrinol 2009; 1: 116-128 DOI: 10.4008/jcrpe.v1i3.49 PMID:21274396

Rapid Communication

Identification of Novel Mutations in STAR Gene in Patients with Lipoid Congenital Adrenal Hyperplasia: A First Report from India
  • Lakshmi Vasudevan
  • Rajesh Joshi
  • Dhanjit Kumar Das
  • Sudha Rao
  • Daksha Sanghavi
  • Shiny Babu
  • Parag M. Tamhankar
J Clin Res Pediatr Endocrinol 2013; 5: 121-124 DOI: 10.4274/Jcrpe.927 PMID:23748066

Case Report

A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency and Turner Syndrome
  • Havva Nur Peltek Kendirci
  • Zehra Aycan
  • Semra Çetinkaya
  • Veysel Nijat Baş
  • Sebahat Yılmaz Ağladıoğlu
  • Aşan Önder
J Clin Res Pediatr Endocrinol 2012; 4: 213-215 DOI: 10.4274/Jcrpe.767 PMID:23261864
High-Dose Hook Effect in 17-Hydroxyprogesterone Assay in a Patient with 21-Hydroxylase Deficiency
  • Mesut Parlak
  • Hamit Yaşar Ellidağ
  • Doğa Türkkahraman
J Clin Res Pediatr Endocrinol 2015; 7: 329-332 DOI: 10.4274/jcrpe.2180 PMID:26777045

Case Report

Does Pseudohypoaldosteronism Mask the Diagnosis of Congenital Adrenal Hyperplasia?
  • Sebahat Yılmaz Ağladıoğlu
  • Zehra Aycan
  • Havva Nur Peltek Kendirci
  • Nilgün Erkek
  • Veysel Nijat Baş
J Clin Res Pediatr Endocrinol 2011; 3: 219-221 DOI: 10.4274/jcrpe.369 PMID:22155467

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