Review
Extensive Literature Review of 46,XX Newborns with Congenital Adrenal Hyperplasia and Severe Genital Masculinization: Should They Be Assigned and Reared Male?
Tom Mazur, Jennifer O’Donnell, Peter A. Lee
Original Article
Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus
Enver Şimşek, Oğuz Çilingir, Tülay Şimşek, et al.
Serum Ghrelin and Glucagon-like Peptide 1 Levels in Children with Prader-Willi and Bardet-Biedl Syndromes
Doğa Türkkahraman, Suat Tekin, Merve Güllü, et al.
Associations of Adipocyte-derived Versican and Macrophage-derived Biglycan with Body Adipose Tissue and Hepatosteatosis in Obese Children
Reyhan Deveci Sevim, Mustafa Gök, Özge Çevik, et al.
Evaluating Postoperative Outcomes and Investigating the Usefulness of EU-TIRADS Scoring in Managing Pediatric Thyroid Nodules Bethesda 3 and 4
Aylin Kılınç Uğurlu, Abdurrahman Bitkay, Fatih Gürbüz, et al.
Microcephaly in Infants: A Retrospective Cohort Study from Turkey
Gonca Keskindemirci, Öykü Özbörü Aşkan, Burak Selver, et al.
Assessment of Executive Function Skills in Children with Isolated Growth Hormone Deficiency: A Cross-sectional Study
Gülsüm Yitik Tonkaz, Atilla Çayır
Salivary Sex Steroid Levels in Infants and the Relation with Infantile Colic
Fulya Mete Kalaycı, Özlem Gürsoy Doruk, İbrahim Mert Erbaş, et al.
Non-thyroidal Illness in Children with Congestive Heart Failure
Biswajit Sahoo, Aashima Dabas, Binita Goswami, et al.
Case Report
Juvenile Granulosa Cell Tumor Mimicking HAIR-AN in a 4-year-old: A Case Report
Rachel Choe Kim, Ilya Goldberg, Trevor Van Brunt, et al.
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deletion Syndrome
Hümeyra Yaşar Köstek, Fatma Özgüç Çömlek, Hakan Gürkan, et al.
Endocrine Evaluation and Homeostatic Model Assessment in Patients with Cornelia de Lange Syndrome
Ángela Ascaso, Ana Latorre-Pellicer, Beatriz Puisac, et al.
Stress Induced Hyperglycemia in Early Childhood as a Clue for the Diagnosis of NEUROD1-MODY
Nur Berna Çelik, Naz Güleray Lafcı, Şenay Savaş-Erdeve, et al.
Successful Management of Severe Hypercalcemia with Zoledronic Acid: A Report of Two Pediatric Cases
Fatih Kilci, Jeremy Huw Jones, Filiz Mine Çizmecioğlu-Jones
Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene
Basma Haris, Idris Mohammed, Umm-Kulthum Ismail Umlai, et al.
Letter to the Editor
Vitamin D Receptor Gene Polymorphisms with Type 1 Diabetes Risk: Correspondence
Hinpetch Daungsupawong, Viroj Wiwanitkit
In response to: “Letter to: Vitamin D Receptor Gene Polymorphisms with Type 1 Diabetes Risk: Correspondence”
Ramasamy Thirunavukkarasu, Ayyappan Chitra, Arthur Asirvatham, et al.
