Review
Managing Paediatric Growth Disorders: Integrating Technology Into a Personalised Approach
Jenny Child, Christine Davies, Katie Frost, et al.
The Effects of Risk Behaviors and Orthorexic Behavior on Glycemic Control in Adolescents with Type 1 Diabetes
Demet Taş, Eda Mengen, Pınar Kocaay, et al.
Intramuscular Short-term ACTH Test for the Determination of Adrenal Function in Children: Safe, Effective and Reliable
Elif Özsu, Zeynep Şıklar, Esra Bilici, et al.
Vitamin D Status Across Age Groups in Turkey: Results of 108,742 Samples from a Single Laboratory
Gül Yeşiltepe-Mutlu, Ekin Deniz Aksu, Abdullah Bereket, et al.
The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey
Gamze Çelmeli, Yusuf Çürek, İkbal Özen Kücükçetin, et al.
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency
Fatma Derya Bulut, Semine Özdemir Dilek, Damla Kotan, et al.
Internipple Distance and Internipple Index in Prepubertal Turkish Girls
Seda Erişen Karaca, Şengül Cangür, İlknur Arslanoğlu
Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism
Muhammet Asena, Meliha Demiral, Edip Unal, et al.
Increased Incidence of Type 1 Diabetes in Children and No Change in the Age of Diagnosis and BMI-SDS at the Onset - is the Accelerator Hypothesis not Working?
Barbara Wasyl-Nawrot, Małgorzata Wójcik, Joanna Nazim, et al.
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants
Tülay Güran, Başak Tezel, Meltem Çakır, et al.
Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of Turkey
Meliha Demiral, Edip Unal, Birsen Baysal, et al.
Children with Hashimoto’s Thyroiditis Have Increased Intestinal Permeability: Results of a Pilot Study
Banu Küçükemre Aydın, Melek Yıldız, Abdurrahman Akgün, et al.
A Duplication Upstream of SOX9 Associated with SRY Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report
Eda Mengen, Gülsüm Kayhan, Pınar Kocaay, et al.
Early Onset Diabetes in Two Children due to Progeria, a Monogenic Disease of DNA Repair
Martin Holder, Valerie Schwitzgebel
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene
Meliha Demiral, Hüseyin Demirbilek, Edip Unal, et al.
