Case Reports

Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in Monozygotic Twins Concordant for Rubinstein-Taybi Syndrome.
  • Mustafa Ali Akın
  • Tamer Güneş
  • Leyla Akın
  • Dilek Çoban
  • Sena Kara Oncu
  • Aslıhan Kiraz
  • Selim Kurtoğlu
J Clin Res Pediatr Endocrinol 2011; 3: 32-35 DOI: 10.4274/jcrpe.v3i1.07 PMID:21448332

Original Article

Developmental Defects of the Thyroid Gland: Relationship with Advanced Maternal Age
  • Heves Kırmızıbekmez
  • Ayla Güven
  • Metin Yıldız
  • Ayşe Nurcan Cebeci
  • Fatma Dursun
J Clin Res Pediatr Endocrinol 2012; 4: 72-75 DOI: 10.4274/Jcrpe.560 PMID:22672863

Case Report

A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome
  • Nusrat Khan
  • Waleed Dandan
  • Noura Al Hassani
  • Suha Hadi
J Clin Res Pediatr Endocrinol 2016; 8: 246-249 DOI: 10.4274/jcrpe.2387 PMID:26761945

Letter to Editor

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis
  • Fatih Gürbüz
  • Serdar Ceylaner
  • Ali Kemal Topaloğlu
  • Bilgin Yüksel
J Clin Res Pediatr Endocrinol 2016; 8: 373-374 DOI: 10.4274/jcrpe.3343

Other

A Case Report of Xp21 Contiguous Gene Syndrome: Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency, and Duchenne Muscular Dystrophy
  • Cengiz Kara
  • Gülay Can Yilmaz
  • Eda Çelebi Bitkin
  • Murat Aydin
J Clin Res Pediatr Endocrinol 2016; 8: 14-15
Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome
  • Banu Sarer Yürekli
  • Nilüfer Özdemir Kutbay
  • Emin Karaca
  • Mehmet Erdoğan
  • Şevki Çetinkalp
  • Ömer Kitiş
  • A. Gökhan Özgen
  • Ferda Özkınay
  • L. Füsun Saygılı
J Clin Res Pediatr Endocrinol 2015; 7: 49-49
Crouzon Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis
  • Fatih Gürbüz
  • Serdar Ceylaner
  • Ali Kemal Topaloğlu
  • Bilgin Yüksel
J Clin Res Pediatr Endocrinol 2015; 7: 83-83

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