E-ISSN: 1308-5735 ISSN: 1308-5727

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Volume 11, Issue 3

September 2019

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Original Article 10

Letter to the Editor 1

Review

Pitfalls with Vitamin D Research in Musculoskeletal Disorders and Recommendations on How to Avoid Them

Gary M. Kiebzak

Pooya Hosseinzadeh

Robert C. Olney

Michael A. Levine

Original Article

Elevated Random Luteinizing Hormone is an Unreliable Indicator for Pubertal Suppression in Girls Treated with Monthly Leuprolide for Idiopathic Central Precocious Puberty

Pattara Wiromrat

Ouyporn Panamonta

Early Menarche is a Risk Factor for Short Stature in Young Korean Females: An Epidemiologic Study

Cases Referred from the Turkish National Screening Program: Frequency of Congenital Hypothyroidism and Etiological Distribution

Zeynep Donbaloğlu

Şenay Savaş-Erdeve

Semra Çetinkaya

Risk Factors for Childhood Overweight and Obesity in Ukraine and Germany

Markus Bettendorf

Natalia Zelinska

Galyna Soloviova

Georg F. Hoffmann

Juergen Grulich-Henn

Evaluation of IGF1/IGFBP3 Molar Ratio as an Effective Tool for Assessing the Safety of Growth Hormone Therapy in Small-for-gestational-age, Growth Hormone-Deficient and Prader-Willi Children

Laurence Périn

Associations Between Serum Uric Acid Concentrations and Cardiometabolic Risk and Renal Injury in Obese and Overweight Children

Deniz Özalp Kızılay

No Associations Between Serum Lipid Levels or HOMA-IR and Asthma in Children and Adolescents: A NHANES Analysis

The Development and Validation of a Turkish Insulin Treatment Self-management Scale Child Form (Ages 8-18) and Parent Form

Çağrı Çövener Özçelik

Nesrin Şen Celasin

Gülten Karahan Okuroğlu

Şükriye Şahin

Antimüllerian Hormone Levels of Infants with Premature Thelarche

Nursel Muratoğlu Şahin

Elvan Bayramoğlu

Hatice Nursun Özcan

Melikşah Keskin

Şenay Savaş-Erdeve

Semra Çetinkaya

Intrauterine Twin Discordancy and Partial Postnatal Catch-up Growth in a Girl with a Pathogenic IGF1R Mutation

Monique Losekoot

Marie J. E. Walenkamp

Christiaan De Bruin

Veronica Mericq

Case Report

A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment

Emine Çamtosun

Ayşehan Akıncı

İbrahim Tekedereli

Ahmet Sığırcı

A Case of the Perinatal Form Hypophosphatasia Caused by a Novel Large Duplication of the ALPL Gene and Report of One Year Follow-up with Enzyme Replacement Therapy

Bülent Hacıhamdioğlu

Gamze Özgürhan

Catarina Pereira

Magnesium and Anti-phosphate Treatment with Bisphosphonates for Generalised Arterial Calcification of Infancy: A Case Report

Tülay Atasoy Öztürk

Heves Kırmızıbekmez

Gülcan Seymen Karabulut

A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic Polyneuropathy

Joanna Oswiecimska

Mateusz Dawidziuk

Katarzyna Ziora

D. Lys Guilbride

Shalini N. Jhangiani

Anna Obuchowicz

James R. Lupski

Wojciech Wiszniewski

Pawel Gawlinski

Letter to the Editor

Vitamin D Deficiency and Insufficiency According to Current Criteria for Children: Vitamin D Status of Elementary School Children in Turkey