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E-ISSN:1308-5735
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ISSN:1308-5727
E-ISSN:1308-5735
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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
Abstract
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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
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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
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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
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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
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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
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Nutrition and Growth
Fima Lifshitz
J Clin Res Pediatr Endocrinol 2009; 1: 157-163
DOI: 10.4274/jcrpe.v1i4.39
PMID:21274290
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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
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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
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Case Report
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
Abstract
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TRMT10A
mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys
Eve Stern
Asaf Vivante
Ortal Barel
Yael Levy-Shraga
J Clin Res Pediatr Endocrinol 0; 0: 0-0
[e-Pub]
DOI: 10.4274/jcrpe.galenos.2020.2020.0265
PMID:33448213
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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
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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
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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
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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
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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
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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
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IGFA Case Report of Pycnodysostosis Associated with Multiple Pituitary Hormone Deficiencies and Response to Treatment
Vishesh Verma
RK Singh
J Clin Res Pediatr Endocrinol 2020; 12: 444-449
DOI: 10.4274/jcrpe.galenos.2020.2019.0194
PMID:32248673
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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
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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
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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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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
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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
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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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Detection of
SHOX
Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature
Semra Gürsoy
Filiz Hazan
Ayça Aykut
Özlem Nalbantoğlu
Hüseyin Anıl Korkmaz
Korcan Demir
Behzat Özkan
Özgür Çoğulu
J Clin Res Pediatr Endocrinol 2020; 12: 358-365
DOI: 10.4274/jcrpe.galenos.2020.2019.0001
PMID:32295321
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