Review
Abnormal Uterine Bleeding In Adolescents
Selin Elmaoğulları, Zehra Aycan
Prevalence and Related Factors of Euthyroid Sick Syndrome in Children with Untreated Cancer According to Two Different Criteria
Ali Duyu, Elvan Çağlar Çıtak, Erdem Ak, et al.
A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations
Aslı Derya Kardelen, Güven Toksoy, Firdevs Baş, et al.
Parental Perception of Terminology of Disorders of Sex Development in Western Turkey
Sibel Tiryaki, Ali Tekin, İsmail Yağmur, et al.
Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty
Zehra Aycan, Şenay Savaş-Erdeve, Semra Çetinkaya, et al.
A Synopsis of Current Practice in the Diagnosis and Management of Patients with Turner Syndrome in Turkey: A Survey of 18 Pediatric Endocrinology Centers
Ahmet Uçar, Ayhan Abacı, Özgür Pirgon, et al.
Subnormal Growth Velocity and Related Factors During GnRH Analog Therapy for Idiopathic Central Precocious Puberty
Nursel Muratoğlu Şahin, Asiye Uğraş Dikmen, Semra Çetinkaya, et al.
Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?
Emine Çamtosun, Zeynep Şıklar, Merih Berberoğlu
Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features
Nataliya Zelinska, Iryna Shevchenko, Evgenia Globa
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life
Filiz Mine Çizmecioğlu, Jeremy Huw Jones, Wendy Forsyth Paterson, et al.
Severe Early Onset Obesity due to a Novel Missense Mutation in Exon 3 of the Leptin Gene in an Infant from Northwest India
Devi Dayal, Keerthivasan Seetharaman, Inusha Panigrahi, et al.
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia
Belma Haliloğlu, Heybet Tüzün, Sarah E. Flanagan, et al.
A Novel Variant c.97C>T of the Growth Hormone Releasing Hormone Receptor Gene Causes Isolated Growth Hormone Deficiency Type Ib
Assimina Galli-Tsinopoulou, Eleni P. Kotanidou, Aggeliki N. Kleisarchaki, et al.
Peripheral Neuropathy as a Complication of Diabetic Ketoacidosis in a Child with Newly Diagnosed Diabetes Type 1: A Case Report
Marta Baszyńska-Wilk, Marta Wysocka-Mincewicz, Anna Świercz, et al.
Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine
Victoria Campbell, Rachel Beckett, Noina Abid, et al.
The Importance of Gestation-Adjusted Birthweight Centile in Assessment of Fetal Growth in Metabolic Conditions
Caroline Ovadia, Hanns-Ulrich Marschall, Catherine Williamson
