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

Syndromic Disorders with Short Stature

• Zeynep Şıklar
• Merih Berberoğlu

The Rationale for Growth Hormone Therapy in Children with Short Stature

• Annalisa Deodati
• Stefano Cianfarani

Controversies in the Definition and Treatment of Idiopathic Short Stature (ISS)

• Stefania Pedicelli
• Emanuela Peschiaroli
• Enrica Violi
• Stefano Cianfarani

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

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

Nutrition and Growth

• Fima Lifshitz

A Review of the Principles of Radiological Assessment of Skeletal Dysplasias

• Yasemin Alanay
• Ralph S. Lachman

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

Case Report

A Case of Familial Male-Limited Precocious Puberty with a Novel Mutation

• Shilpa Gurnurkar
• Emily DiLillo
• Mauri Carakushansky

TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys

• Eve Stern
• Asaf Vivante
• Ortal Barel
• Yael Levy-Shraga

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

3M Syndrome: A Report of Four Cases in Two Families

• Ayla Güven
• Ayşe Nurcan Cebeci

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

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

Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report

• Ahmad Kautsar
• Jan M. Wit
• Aman Pulungan

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

IGFA Case Report of Pycnodysostosis Associated with Multiple Pituitary Hormone Deficiencies and Response to Treatment

• Vishesh Verma
• RK Singh

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

Case Report

An Unusual Combination of Klinefelter Syndrome and Growth Hormone Deficiency in a Prepubertal Child

• Jayanthy Ramesh
• Mudiganti Nagasatyavani
• Javvadii Venkateswarlu
• Jakka Nagender

Hypochondroplasia in a Child with 1620C>G (Asn540Lys) Mutation in FGFR3

• Hüseyin Anıl Korkmaz
• Filiz Hazan
• Ceyhun Dizdarer
• Ajlan Tükün

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

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

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

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