Review

Important Tools for Use by Pediatric Endocrinologists in the Assessment of Short Stature
  • José I. Labarta
  • Michael B. Ranke
  • Mohamad Maghnie
  • David Martin
  • Laura Guazzarotti
  • Roland Pfäffle
  • Ekaterina Koledova
  • Jan M. Wit
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2020.2020.0206 PMID:33006554
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
New Features for Child Metrics: Further Growth References and Blood Pressure Calculations
  • Korcan Demir
  • Ergun Konakçı
  • Güven Özkaya
  • Belde Kasap Demir
  • Samim Özen
  • Murat Aydın
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2020; 12: 125-129 DOI: 10.4274/jcrpe.galenos.2019.2019.0127 PMID:31475511
A Proposal for the Interpretation of Serum IGF-I Concentration as Part of Laboratory Screening in Children with Growth Failure
  • Jan M. Wit
  • Martin Bidlingmaier
  • Christiaan de Bruin
  • Wilma Oostdijk
J Clin Res Pediatr Endocrinol 2020; 12: 130-139 DOI: 10.4274/jcrpe.galenos.2019.2019.0176 PMID:31842524
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
Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy
  • Jan M. Wit
  • Asma Deeb
  • Bassam Bin-Abbas
  • Angham Al Mutair
  • Ekaterina Koledova
  • Martin O. Savage
J Clin Res Pediatr Endocrinol 2019; 11: 329-340 DOI: 10.4274/jcrpe.galenos.2019.2019.0088 PMID:31284701

Case Report

A Case Report of Pycnodysostosis Associated with Multiple Pituitary Hormone Deficiencies and Response to Treatment
  • Vishesh Verma
  • RK Singh
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2020.2019.0104 PMID:32248673
A Case of Familial Male-Limited Precocious Puberty with a Novel Mutation
  • Shilpa Gurnurkar
  • Emily DiLillo
  • Mauri Carakushansky
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2020.2020.0067 PMID:32757547
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
A Case of Cleidocranial Dysplasia 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 2019; 11: 301-305 DOI: 10.4274/jcrpe.galenos.2018.2018.0211 PMID:30468148
Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report
  • Ahmad Kautsar
  • Jan M. Wit
  • Aman Pulungan
J Clin Res Pediatr Endocrinol 2019; 11: 426-431 DOI: 10.4274/jcrpe.galenos.2019.2018.0305 PMID:30678423
A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent
  • Şükran Poyrazoğlu
  • Vivian Hwa
  • Firdevs Baş
  • Andrew Dauber
  • Ron Rosenfeld
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2019; 11: 432-438 DOI: 10.4274/jcrpe.galenos.2019.2018.0301 PMID:30717585

Original Article

Detection of SHOX Gene Variations in Patients Who Had Skeletal Abnormalities With/Without Short Stature
  • Semra Gürsoy
  • Filiz Hazan
  • Ayça Aykut
  • Özlem Nalbantoğlu
  • Hüseyin Anıl Korkmaz
  • Korcan Demir
  • Behzat Özkan
  • Özgür Çogulu
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2020.2020.0001 PMID:32295321
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
Early Menarche is a Risk Factor for Short Stature in Young Korean Females: An Epidemiologic Study
  • Sol Kang
  • Yoon Mo Kim
  • Jun Ah Lee
  • Dong Ho Kim
  • Jung Sub Lim
J Clin Res Pediatr Endocrinol 2019; 11: 234-239 DOI: 10.4274/jcrpe.galenos.2018.2018.0274 PMID:30604602
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

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

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