Review
Endocrinologic Consequences of Pediatric Posterior Fossa Tumours
Abdullah Bereket
Original Article
Diagnostic Work-up and Follow-up in Children with Tall Stature: A Simplified Algorithm for Clinical Practice
Susanne E. Stalman, Anke Pons, Jan M. Wit, et al.
Low-Grade Inflammation and Increased Arterial Stiffness in Chinese Youth and Adolescents with Newly-Diagnosed Type 2 Diabetes Mellitus
Xin Li, You Ping Deng, Miao Yang, et al.
Neutrophil Gelatinase-Associated Lipocalin as an Early Sign of Diabetic Kidney Injury in Children
Zeynep Yürük Yıldırım, Ahmet Nayır, Alev Yılmaz, et al.
Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children
Olcay Neyzi, Rüveyde Bundak, Gülbin Gökçay, et al.
Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience
Pamir Gülez, Hüseyin Anıl Korkmaz, Dilek Özkök, et al.
The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels
Zeynep Şıklar, Pınar Kocaay, Emine Çamtosun, et al.
Cardiac Function in Newborns with Congenital Hypothyroidism: Association with Thyroid-Stimulating Hormone Levels
Taliha Öner, Rahmi Özdemir, Önder Doksöz, et al.
Educational Needs of Adolescents Regarding Normal Puberty and Menstrual Patterns
Pınar İşgüven, Göze Yörük, Filiz Mine Çizmecioğlu
A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family
Hakan Cangül, Murat Doğan, Duran Üstek
Case Report
High-Dose Hook Effect in 17-Hydroxyprogesterone Assay in a Patient with 21-Hydroxylase Deficiency
Mesut Parlak, Hamit Yaşar Ellidağ, Doğa Türkkahraman
An Unusual Presentation of Parathyroid Adenoma in an Adolescent: Calcific Achilles Tendinitis
Selim Kurtoğlu, Leyla Akın, Mustafa Kendirci, et al.
Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype
Özge Yüce, Esra Döğer, Nurullah Çelik, et al.
Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report
Erkan Sarı, Erman Ataş, Engin Burak Bulut, et al.
A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome
Gül Yeşiltepe Mutlu, Heves Kırmızıbekmez, Akie Nakamura, et al.
Hyperthyroidism After Allogeneic Hematopoietic Stem Cell Transplantation: A Report of Four Cases
Erdal Sağ, Nazlı Gönç, Ayfer Alikaşifoğlu, et al.
Letter to Editor
Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
Korcan Demir, Özlem Nalbantoğlu, Kadri Karaer, et al.
