Review
Traditional and New Methods of Bone Age Assessment-An Overview
Monika Prokop-Piotrkowska, Kamila Marszałek-Dziuba, Elżbieta Moszczyńska, et al.
Pre-treatment Neutropenia in Children and Adolescents with Autoimmune Hyperthyroidism
Melissa Kaori S. Litao, Ana Gutierrez Alvarez, Bina Shah
Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism
Ceren Günbey, Alev Özön, E. Nazlı Gönç, et al.
Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience
Selin Elmaoğulları, Şervan Özalkak, Semra Çetinkaya, et al.
An Evaluation of Glucagon Injection Anxiety and Its Association with the Fear of Hypoglycemia among the Parents of Children with Type 1 Diabetes
Serra Muradoğlu, Gül Yeşiltepe Mutlu, Tuğba Gökçe, et al.
Midkine: Utility as a Predictor of Early Diabetic Nephropathy in Children with Type 1 Diabetes Mellitus
Kotb Abbass Metwalley, Hekma Saad Farghaly, Magda Farghali Gabri, et al.
Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia
Elvan Bayramoğlu, Melikşah Keskin, Zehra Aycan, et al.
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome
Aydilek Dağdeviren Çakır, Firdevs Baş, Onur Akın, et al.
The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region
Sinem Yalçıntepe, Fatma Özgüç Çömlek, Hakan Gürkan, et al.
Evaluation of Growth Hormone Results in Different Diagnosis and Trend Over 10 Year of Follow-up: A Single Center Experience
Zehra Aycan, Aslıhan Araslı Yılmaz, Servet Yel, et al.
Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations
Begümhan Demir Gündoğan, Fatih Sağcan, Sevcan Tuğ Bozdoğan, et al.
Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
Carla Bizzarri, Germana Antonella Giannone, Jacopo Gervasoni, et al.
A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene
Doğa Türkkahraman, Nimet Karataş Torun, Nadide Cemre Randa
Brain Abscess in a Patient with Osteopetrosis: A Rare Complication
Merve İşeri Nepesov, Eylem Kıral, Gürkan Bozan, et al.
In reply Asif M et al.
Muhammad Asif, Muhammad Aslam
