Case Report

A Cleidocranial Dysplasia Case with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment
  • Emine Çamtosun
  • Ayşehan Akıncı
  • Emine Demiral
  • İbrahim Tekedereli
  • Ahmet Sığırcı
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.0211
Syndrome of Extreme Insulin Resistance 
(Rabson-Mendenhall Phenotype) with Atrial Septal Defect: Clinical Presentation and Treatment Outcomes
  • Deep Dutta
  • Indira Maisnam
  • Sujoy Ghosh
  • Satinath Mukhopadhyay
  • Subhankar Chowdhury
J Clin Res Pediatr Endocrinol 2013; 5: 58-61 DOI: 10.4274/Jcrpe.857 PMID:23367497
3M Syndrome: A Report of Four Cases in Two Families
  • Ayla Güven
  • Ayşe Nurcan Cebeci
J Clin Res Pediatr Endocrinol 2011; 3: 154-159 DOI: 10.4274/jcrpe.v3i3.30 PMID:21911330
A Novel Variant c.97C>T of the Growth Hormone Releasing Hormone Receptor Gene Causes Isolated Growth Hormone Deficiency Type Ib
  • Assimina Galli-Tsinopoulou
  • Eleni P. Kotanidou
  • Aggeliki N. Kleisarchaki
  • Rivka Kauli
  • Zvi Laron
J Clin Res Pediatr Endocrinol 2018; 10: 284-288 DOI: 10.4274/jcrpe.5188 PMID:29537382

Review

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
The Rationale for Growth Hormone Therapy in Children with Short Stature
  • Annalisa Deodati
  • Stefano Cianfarani
J Clin Res Pediatr Endocrinol 2017; 9: 23-32 DOI: 10.4274/jcrpe.2017.S003 PMID:29280742
Controversies in the Definition and Treatment of Idiopathic Short Stature (ISS)
  • Stefania Pedicelli
  • Emanuela Peschiaroli
  • Enrica Violi
  • Stefano Cianfarani
J Clin Res Pediatr Endocrinol 2009; 1: 105-115 DOI: 10.4008/jcrpe.v1i3.53 PMID:21274395
Nutrition and Growth
  • Fima Lifshitz
J Clin Res Pediatr Endocrinol 2009; 1: 157-163 DOI: 10.4274/jcrpe.v1i4.39 PMID:21274290
A Review of the Principles of Radiological Assessment of Skeletal Dysplasias
  • Yasemin Alanay
  • Ralph S. Lachman
J Clin Res Pediatr Endocrinol 2011; 3: 163-178 DOI: 10.4274/jcrpe.463 PMID:22155458

Original Research

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature
  • Kenan Delil
  • Halil Gürhan Karabulut
  • Bülent Hacıhamdioğlu
  • Zeynep Şıklar
  • Merih Berberoğlu
  • Gönül Öçal
  • Ajlan Tükün
  • Hatice Ilgın Ruhi
J Clin Res Pediatr Endocrinol 2016; 8: 144-149 DOI: 10.4274/jcrpe.2307 PMID:26758084

Case Report

An Unusual Combination of Klinefelter Syndrome and Growth Hormone Deficiency in a Prepubertal Child
  • Jayanthy Ramesh
  • Mudiganti Nagasatyavani
  • Javvadii Venkateswarlu
  • Jakka Nagender
J Clin Res Pediatr Endocrinol 2014; 6: 187-189 DOI: 10.4274/jcrpe.1225 PMID:25241616
Hypochondroplasia in a Child with 1620C>G (Asn540Lys) Mutation in FGFR3
  • Hüseyin Anıl Korkmaz
  • Filiz Hazan
  • Ceyhun Dizdarer
  • Ajlan Tükün
J Clin Res Pediatr Endocrinol 2012; 4: 220-222 DOI: 10.4274/Jcrpe.787 PMID:23149434

Original Article

Novel Growth Hormone-Releasing Hormone Receptor Gene Mutations in Turkish Children with Isolated Growth Hormone Deficiency
  • Ahmet Arman
  • Bumin Nuri Dündar
  • Ergun Çetinkaya
  • Nilüfer Erzaim
  • Atilla Büyükgebiz
J Clin Res Pediatr Endocrinol 2014; 6: 202-208 DOI: 10.4274/jcrpe.1518 PMID:25541890
The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels
  • Zeynep Şıklar
  • Pınar Kocaay
  • Emine Çamtosun
  • Mehmet İsakoca
  • Bülent Hacıhamdioğlu
  • Şenay Savaş Erdeve
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2015; 7: 301-306 DOI: 10.4274/jcrpe.2111 PMID:26777041

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