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

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Volume 8, Issue 2

June 2016

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Editor’s Note 1

Original Research 14

Editor’s Note

Editor’s Note

Feyza Darendeliler

Review

Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects

Selim Kurtoğlu

Original Research

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

Leman Damla Kotan

Charlton Cooper

Şükran Darcan

Mohammad K. Hamedani

A. Kemal Topaloğlu

Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

Halil Gürhan Karabulut

Bülent Hacıhamdioğlu

Zeynep Şıklar

Merih Berberoğlu

Hatice Ilgın Ruhi

Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto’s Thyroiditis

Pınar İşgüven

Yasemin Gündüz

Mukaddes Kılıç

Thyroid Function and Thyroid Autoimmunity in Relation to Weight Status and Cardiovascular Risk Factors in Children and Adolescents: A Population-Based Study

Emilio García-García

María A. Vázquez-López

Eduardo García-Fuentes

Rafael Galera-Martínez

Carolina Gutiérrez-Repiso

Icíar García-Escobar

Antonio Bonillo-Perales

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

Mehmet Nuri Özbek

Hüseyin Demirbilek

Rıza Taner Baran

Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course

Gülay Can Yılmaz

Cellular Trace Element Changes in Type 1 Diabetes Patients

Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey

Nilgün Çaylan

Bekir Keskinkılıç

Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey

Hepsen Mine Serin

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

Ayşe Nurcan Cebeci

Sarah E. Flanagan

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans

Doğa Türkkahraman

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Şenay Savaş-Erdeve

Zeynep Şıklar

Bülent Hacıhamdioğlu

Emine Çamtosun

Merih Berberoğlu

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

Sevim Karakaş Çelik

Case Report

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

Adrijan Sarajlija

Tatjana Milenkovic

Maja Djordjevic

Katarina Mitrovic

Sladjana Todorovic

A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty

Cemil Koçyiğit

Serdar Sarıtaş

Gönül Çatlı

Bumin Nuri Dündar

Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene

Hana Al Suwaidi

Fakunle Ibukunoluwa

A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient

Chutintorn Sriphrapradang

Yotsapon Thewjitcharoen

Suwannee Chanprasertyothin

Soontaree Nakasatien

Thep Himathongkam

A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome

Noura Al Hassani

Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports

Valeria Calcaterra

Maria Luisa Fonte

Michela Albanesi