Original Research
Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation
Şükran Poyrazoğlu, Rüveyde Bundak, Firdevs Baş, et al.
Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years
Wei-Yan Wang, Yi Sun, Wen-Ting Zhao, et al.
The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome
Abdurrahman Kaya, Cemil Koçyiğit, Gönül Çatlı, et al.
Treatment of Pre-pubertal Patients with Growth Hormone Deficiency: Patterns in Growth Hormone Dosage and Insulin-like Growth Factor-I Z-scores
Megan Oberle, Adda Grimberg, Vaneeta Bamba
Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents
Selma Tunç, Korcan Demir, Fatma Ajlan Tükün, et al.
Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases
Emre Divarcı, Ülgen Çeltik, Zafer Dökümcü, et al.
Clinical and Genetic Findings of Turkish Hypophosphatasia Cases
Halil Sağlam, Şahin Erdöl, Sevil Dorum
The Relationship of Disordered Eating Attitudes with Stress Level, Bone Turnover Markers, and Bone Mineral Density in Obese Adolescents
Aslı Okbay Güneş, Müjgan Alikaşifoğlu, Ezgi Şen Demirdöğen, et al.
Phenotype Heterogeneity in Glucokinase–Maturity-Onset Diabetes of the Young (GCK-MODY) Patients
Anna Wedrychowicz, Ewa Tobór, Magdalena Wilk, et al.
The Relationship Between Perceived Family Climate and Glycemic Control in Type 1 Diabetes Mellitus Adolescent Patients
Şafak Eray, Halit Necmi Uçar, Fatma Çetinkaya, et al.
An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression
Sarah E. Flanagan, Vu Chí Dung, Jayne A. L. Houghton, et al.
Pituitary Adenoma Apoplexy in an Adolescent: A Case Report and Review of the Literature
Hero Zijlker, Sebastian Schagen, Jan Maarten Wit, et al.
Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene
Monica Gabbay, Sian Ellard, Elisa De Franco, et al.
Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings
Bayram Özhan, Özlem Boz Anlaş, Bilge Sarıkepe, et al.
Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy
E. Nazlı Gönç, Alev Özön, Ayfer Alikaşifoğlu, et al.
Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases
Gerdi Tuli, Daniele Tessaris, Silvia Einaudi, et al.
