E-ISSN: 1308-5735 ISSN: 1308-5727

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Volume 10, Issue 3

September 2018

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Original Article 9

Letter to the Editor 1

Review

Abnormal Uterine Bleeding In Adolescents

Selin Elmaoğulları

Original Article

Prevalence and Related Factors of Euthyroid Sick Syndrome in Children with Untreated Cancer According to Two Different Criteria

Elvan Çağlar Çıtak

Begül Yağcı Küpeli

İbrahim Bayram

Gülçin Eskendari

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

Zehra Yavaş Abalı

Şükran Poyrazoğlu

Rüveyde Bundak

Umut Altunoğlu

Feyza Darendeliler

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

İsmail Yağmur

Şükran Darcan

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Şenay Savaş-Erdeve

Semra Çetinkaya

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

Filiz Tütüncüler

Gönül Çatlı

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

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

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

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

Keerthivasan Seetharaman

Inusha Panigrahi

Balasubramaniyan Muthuvel

Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia

Belma Haliloğlu

Sarah E. Flanagan

Muhittin Çelik

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

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

Jolanta Świderska

Magdalena Marszał

Mieczysław Szalecki

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

Victoria Campbell

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