Review

Newborn Screening for Congenital Hypothyroidism

• Atilla Büyükgebiz

Original Research

Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis

• Shiguo Liu
• Jian Chai
• Guohua Zheng
• Huichao Li
• Deguo Lu
• Yinlin Ge

Recognizing the Psychosocial Aspects of Type 1 Diabetes in Adolescents

• Erdal Adal
• Zerrin Önal
• Atilla Ersen
• Koray Yalçın
• Hasan Önal
• Ahmet Aydın

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

• Pınar İşgüven
• Yasemin Gündüz
• Mukaddes Kılıç

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

• Cengiz Kara
• Figen Günindi
• Gülay Can Yılmaz
• Murat Aydın

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

• Sema Akçurin
• Doğa Türkkahraman
• Woo-Young Kim
• Erdem Durmaz
• Jae-Gook Shin
• Su-Jun Lee

Clinical and Genetic Findings of Turkish Hypophosphatasia Cases

• Halil Sağlam
• Şahin Erdöl
• Sevil Dorum

Original Article

Time Trends, Regional Variability and Seasonality Regarding the Incidence of Type 1 Diabetes Mellitus in Romanian Children Aged 0-14 Years, Between 1996 and 2015

• Adrian Vlad
• Viorel Serban
• Anders Green
• Sören Möller
• Mihaela Vlad
• Bogdan Timar
• Alexandra Sima
• on behalf of the ONROCAD Study Group

Serum Paraoxonase/Arylesterase Activity and Oxidative Stress Status in Children with Metabolic Syndrome

• Erdal Eren
• Mahmut Abuhandan
• Abdullah Solmaz
• Abdullah Taşkın

Original Article

Weight and Height Percentiles For 0-84- Month-Old Children in Kayseri - A Central Anatolian City in Turkey

• Canan Altunay
• Meda Kondolot
• Serpil Poyrazoğlu
• Ahmet Öztürk
• Mümtaz M. Mazıcıoğlu
• Selim Kurtoğlu

Case Report

Weismann-Netter-Stuhl Syndrome:A family report

• Hayrullah Alp
• Mehmet Emre Atabek
• Özgür Pirgon

Atypical Presentation of Hashimoto’s Disease in an Adolescent: Thyroid-Associated Ophthalmopathy

• Heves Kırmızıbekmez
• Rahime Gül Yeşiltepe Mutlu
• Fatma Dursun
• Murat Günay

Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings

• Bayram Özhan
• Özlem Boz Anlaş
• Bilge Sarıkepe
• Burcu Albuz
• Nur Semerci Gündüz

Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases

• Gerdi Tuli
• Daniele Tessaris
• Silvia Einaudi
• Luisa De Sanctis
• Patrizia Matarazzo

Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype

• Özge Yüce
• Esra Döğer
• Nurullah Çelik
• Hamdi Cihan Emeksiz
• Mahmut Orhun Çamurdan
• Aysun Bideci
• Peyami Cinaz