Review

Syndromic Disorders Caused by Disturbed Human Imprinting
  • Diana Carli
  • Evelise Riberi
  • Giovanni Battista Ferrero
  • Alessandro Mussa
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2019.2018.0249 PMID:30968677
Syndromic Disorders with Short Stature
  • Zeynep Şıklar
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2014; 6: 1-8 DOI: 10.4274/Jcrpe.1149 PMID:24637303

Original Article

Neurocognitive Functions in Children and Adolescents with Subclinical Hypothyroidism
  • Ayça Törel Ergür
  • Yasemen Taner
  • Evşen Ata
  • Efnan Melek
  • Emel Erdoğan Bakar
  • Tanzer Sancak
J Clin Res Pediatr Endocrinol 2012; 4: 21-24 DOI: 10.4274/Jcrpe.497 PMID:22394701
Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
  • Helmuth G. Dörr
  • Theresa Penger
  • Andrea Albrecht
  • Michaela Marx
  • Thomas M. K. Völkl
J Clin Res Pediatr Endocrinol 2019; 11: 41-45 DOI: 10.4274/jcrpe.galenos.2018.2018.0149 PMID:30178749
Long-Term Treatment with n-3 Polyunsaturated Fatty Acids as a Monotherapy in Children with Nonalcoholic Fatty Liver Disease
  • Mehmet Boyraz
  • Özgür Pirgon
  • Bumin Dündar
  • Ferhat Çekmez
  • Nihal Hatipoğlu
J Clin Res Pediatr Endocrinol 2015; 7: 121-127 DOI: 10.4274/jcrpe.1749 PMID:26316434
The Association Between Maternal Subclinical Hypothyroidism and Growth, Development, and Childhood Intelligence: A Meta-analysis
  • Yahong Liu
  • Hui Chen
  • Chen Jing
  • FuPin Li
J Clin Res Pediatr Endocrinol 2018; 10: 153-161 DOI: 10.4274/jcrpe.4931 PMID:28958983
Assessment of Cardiovascular Parameters in Obese Children and Adolescents with Non-Alcoholic Fatty Liver Disease
  • Beray Selver Eklioğlu
  • Mehmet Emre Atabek
  • Nesibe Akyürek
  • Hayrullah Alp
J Clin Res Pediatr Endocrinol 2015; 7: 222-227 DOI: 10.4274/jcrpe.1949 PMID:26831557

Case Reports

Al-Awadi/Raas-Rothschild Syndrome in a Newborn with Additional Anomalies
  • Esma Alp
  • Hayrullah Alp
  • Mehmet Emre Atabek
  • Özgür Pirgon
J Clin Res Pediatr Endocrinol 2010; 2: 49-51 DOI: 10.4274/jcrpe.v2i1.49 PMID:21274338

Case Report

Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
  • Feryal Karahan
  • Elvan Çağlar Çıtak
  • Emel Yaman
  • Mehmet Alakaya
  • Fatih Sağcan
  • Eda Bengi Yılmaz
  • Funda Kuş
  • İclal Gürses
  • Yüksel Balcı
J Clin Res Pediatr Endocrinol 2018; 10: 87-90 DOI: 10.4274/jcrpe.4905 PMID:28836496
Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene
  • Ercan Mıhçı
  • Doğa Tu¨rkkahraman
  • Sian Ellard
  • Sema Akçurin
  • İffet Bircan
J Clin Res Pediatr Endocrinol 2012; 4: 101-103 DOI: 10.4274/Jcrpe.619 PMID:22672868
An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report
  • Dulika Sumathipala
  • Thilini Gamage
  • Bandula Wijesiriwardena
  • Rohan W. Jayasekara
  • Vajira H.W. Dissanayake
J Clin Res Pediatr Endocrinol 2012; 4: 223-225 DOI: 10.4274/Jcrpe.764 PMID:23032147
Importance of Insulin Immunoassays in the Diagnosis of Factitious Hypoglycemia
  • Özlem Nalbantoğlu Elmas
  • Korcan Demir
  • Nusret Soylu
  • Nilüfer Çelik
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2014; 6: 258-261 DOI: 10.4274/jcrpe.1492 PMID:25541899
Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene
  • Monica Gabbay
  • Sian Ellard
  • Elisa De Franco
  • Regina S. Moisés
J Clin Res Pediatr Endocrinol 2017; 9: 274-277 DOI: 10.4274/jcrpe.4494 PMID:28663161
A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome
  • Gül Yeşiltepe Mutlu
  • Heves Kırmızıbekmez
  • Akie Nakamura
  • Maki Fukami
  • Şükrü Hatun
J Clin Res Pediatr Endocrinol 2015; 7: 344-348 DOI: 10.4274/jcrpe.2249 PMID:26777049

Original Research

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
Cellular Trace Element Changes in Type 1 Diabetes Patients
  • Vahap Uğurlu
  • Çiğdem Binay
  • Enver Şimşek
  • Cengiz Bal
J Clin Res Pediatr Endocrinol 2016; 8: 180-186 DOI: 10.4274/jcrpe.2449 PMID:27086726
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
Clinical and Genetic Findings of Turkish Hypophosphatasia Cases
  • Halil Sağlam
  • Şahin Erdöl
  • Sevil Dorum
J Clin Res Pediatr Endocrinol 2017; 9: 229-236 DOI: 10.4274/jcrpe.4549 PMID:28663156
The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats
  • Erdoğan Özgür
  • Börte Gürbüz Özgür
  • Hatice Aksu
  • Gökhan Cesur
J Clin Res Pediatr Endocrinol 2016; 8: 439-444 DOI: 10.4274/jcrpe.3498 PMID:27611926

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