Review
Pitfalls with Vitamin D Research in Musculoskeletal Disorders and Recommendations on How to Avoid Them
Gary M. Kiebzak, Kevin M. Neal, Pooya Hosseinzadeh, et al.
Early Menarche is a Risk Factor for Short Stature in Young Korean Females: An Epidemiologic Study
Sol Kang, Yoon Mo Kim, Jun Ah Lee, et al.
Cases Referred from the Turkish National Screening Program: Frequency of Congenital Hypothyroidism and Etiological Distribution
Zeynep Donbaloğlu, Şenay Savaş-Erdeve, Semra Çetinkaya, et al.
Risk Factors for Childhood Overweight and Obesity in Ukraine and Germany
Vira Yakovenko, Laura Henn, Markus Bettendorf, et al.
Associations Between Serum Uric Acid Concentrations and Cardiometabolic Risk and Renal Injury in Obese and Overweight Children
Deniz Özalp Kızılay, Semra Şen, Betül Ersoy
No Associations Between Serum Lipid Levels or HOMA-IR and Asthma in Children and Adolescents: A NHANES Analysis
Min Lu, Beirong Wu, Rong Qiao, et al.
The Development and Validation of a Turkish Insulin Treatment Self-management Scale Child Form (Ages 8-18) and Parent Form
Çağrı Çövener Özçelik, Eda Aktaş, Nesrin Şen Celasin, et al.
Antimüllerian Hormone Levels of Infants with Premature Thelarche
Nursel Muratoğlu Şahin, Elvan Bayramoğlu, Hatice Nursun Özcan, et al.
Intrauterine Twin Discordancy and Partial Postnatal Catch-up Growth in a Girl with a Pathogenic IGF1R Mutation
Paula Ocaranza, Monique Losekoot, Marie J. E. Walenkamp, et al.
A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment
Emine Çamtosun, Ayşehan Akıncı, Emine Demiral, et al.
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, et al.
Magnesium and Anti-phosphate Treatment with Bisphosphonates for Generalised Arterial Calcification of Infancy: A Case Report
Fatma Dursun, Tülay Atasoy Öztürk, Serçin Güven, et al.
A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic Polyneuropathy
Joanna Oswiecimska, Mateusz Dawidziuk, Tomasz Gambin, et al.
