Review

Abnormal Uterine Bleeding In Adolescents

• Selin Elmaoğulları
• Zehra Aycan

Original Article

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
• Serhan Kupeli
• Begül Yağcı Küpeli
• İbrahim Bayram
• Gülay Sezgin
• Gülçin Eskendari
• Kerem Sezer

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
• Zehra Yavaş Abalı
• Genco Gençay
• Şükran Poyrazoğlu
• Rüveyde Bundak
• Umut Altunoğlu
• Şahin Avcı
• Adam Najaflı
• Oya Uyguner
• Birsen Karaman
• Seher Başaran
• Feyza Darendeliler

Parental Perception of Terminology of Disorders of Sex Development in Western Turkey

• Sibel Tiryaki
• Ali Tekin
• İsmail Yağmur
• Samim Özen
• Burcu Özbaran
• Damla Gökşen
• Şükran Darcan
• İbrahim Ulman
• Ali Avanoğlu

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

• Zehra Aycan
• Şenay Savaş-Erdeve
• Semra Çetinkaya
• Erdal Kurnaz
• Melikşah Keskin
• Nursel Muratoğlu Şahin
• Elvan Bayramoğlu
• Gülay Ceylaner

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
• Bumin Dündar
• Filiz Tütüncüler
• Gönül Çatlı
• Ahmet Anık
• Aylin Kılınç Uğurlu
• Atilla Büyükgebiz
• (Turner Study Group)

Subnormal Growth Velocity and Related Factors During GnRH Analog Therapy for Idiopathic Central Precocious Puberty

• Nursel Muratoğlu Şahin
• Asiye Uğraş Dikmen
• Semra Çetinkaya
• Zehra Aycan

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
• Sakina Kherra
• Mariam Kourime
• Ruth McGowan
• M. Guftar Shaikh
• Malcolm Donaldson

Case Report

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
• Balasubramaniyan Muthuvel
• Ashish Agarwal

Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia

• Belma Haliloğlu
• Heybet Tüzün
• Sarah E. Flanagan
• Muhittin Çelik
• Avni Kaya
• Sian Ellard
• Mehmet Nuri Özbek

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
• Rivka Kauli
• Zvi Laron

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
• Jolanta Świderska
• Magdalena Marszał
• Mieczysław Szalecki

Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine

• Victoria Campbell
• Rachel Beckett
• Noina Abid
• Susannah Hoey

Letter to the Editor

The Importance of Gestation-Adjusted Birthweight Centile in Assessment of Fetal Growth in Metabolic Conditions

• Caroline Ovadia
• Hanns-Ulrich Marschall
• Catherine Williamson