
Original Article
Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations
Gamze Akkuş, Leman Damla Kotan, Erdem Durmaz, et al.
Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche
Mesut Parlak, Doğa Türkkahraman, Hamit Yaşar Ellidağ, et al.
Congenital Hypothyroidism and Bone Remodeling Cycle
Nazmi Mutlu Karakaş, Sibel Tulgar Kınık, Beril Özdemir, et al.
Association Between Obesity and Parental Weight Status in Children and Adolescents
Maryam Bahreynian, Mostafa Qorbani, Bita Moradi Khaniabadi, et al.
Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis
Fatma Hilal Yılmaz, Sevil Arı Yuca, Hüsamettin Vatansev, et al.
Serum Irisin and Oxytocin Levels as Predictors of Metabolic Parameters in Obese Children
Çiğdem Binay, Cem Paketçi, Savaş Güzel, et al.
Higher-Than-Conventional Subcutaneous Regular Insulin Doses Following Diabetic Ketoacidosis in Children and Adolescents
Özlem Bağ, Selma Tunç, Özlem Nalbantoğlu, et al.
Gene Polymorphisms of Glutathione S-Transferase T1/M1 in Egyptian Children and Adolescents with Type 1 Diabetes Mellitus
Naglaa Barseem, Mona Elsamalehy
Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children
Edip Unal, Alper Akın, Ruken Yıldırım, et al.
Can Stoss Therapy Be Used in Children with Vitamin D Deficiency or Insufficiency without Rickets?
Cemil Koçyiğit, Gönül Çatlı, Gülberat İnce, et al.
Menarcheal Age and Risk of Type 2 Diabetes: A Community-Based Cohort Study
Maryam Farahmand, Fahimeh Ramezani Tehrani, Marzieh Rostami Dovom, et al.
Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign
Emine Çamtosun, Zeynep Şıklar, Serdar Ceylaner, et al.
Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor
Merve Koç Yekedüz, Zeynep Şıklar, Berk Burgu, et al.
The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D3-Resistant Rickets
Ayşehan Akıncı, İsmail Dündar, Meltem Kıvılcım
Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Novel Anti-Müllerian Hormone Receptor Mutation
Özlem Korkmaz, Samim Özen, Nurhan Özcan, et al.
A Comprehensive Online Calculator for Pediatric Endocrinologists: ÇEDD Çözüm/TPEDS Metrics
Korcan Demir, Samim Özen, Ergun Konakçı, et al.


