Editor’s Note
Editor’s Note
Feyza Darendeliler
Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects
Levent Korkmaz, Osman Baştuğ, Selim Kurtoğlu
Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1
Leman Damla Kotan, Charlton Cooper, Şükran Darcan, et al.
Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis
Shan Bao, Jun-Hong Cai, Shu-Ying Yang, et al.
Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature
Kenan Delil, Halil Gürhan Karabulut, Bülent Hacıhamdioğlu, et al.
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, et al.
Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism
Mehmet Nuri Özbek, Hüseyin Demirbilek, Rıza Taner Baran, et al.
Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course
Cengiz Kara, Figen Günindi, Gülay Can Yılmaz, et al.
Cellular Trace Element Changes in Type 1 Diabetes Patients
Vahap Uğurlu, Çiğdem Binay, Enver Şimşek, et al.
Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey
Nilgün Çaylan, Başak Tezel, Sema Özbaş, et al.
Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey
İhsan Esen, Baran Oğuz, Hepsen Mine Serin
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism
Ayla Güven, Ayşe Nurcan Cebeci, Sian Ellard, et al.
A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans
Sema Akçurin, Doğa Türkkahraman, Woo-Young Kim, et al.
Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height
Şenay Savaş-Erdeve, Zeynep Şıklar, Bülent Hacıhamdioğlu, et al.
Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
Erdal Eren, Tuba Edgünlü, Emre Asut, et al.
A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism
Xiao Zheng, Shao-Gang Ma, Ya-Li Qiu, et al.
Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients
Adrijan Sarajlija, Tatjana Milenkovic, Maja Djordjevic, et al.
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, et al.
Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene
Asma Deeb, Hana Al Suwaidi, Fakunle Ibukunoluwa, et al.
A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient
Chutintorn Sriphrapradang, Yotsapon Thewjitcharoen, Suwannee Chanprasertyothin, et al.
A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome
Nusrat Khan, Waleed Dandan, Noura Al Hassani, et al.
Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports
Valeria Calcaterra, Hellas Cena, Maria Luisa Fonte, et al.
