| Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects | LEVENT KORKMAZ,Osman BAŞTUĞ,Selim KURTOĞLU | 114–124 |
| Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1 | LEMAN DAMLA KOTAN GEDİK,Charlton COOPER,ŞÜKRAN DARCAN,Ian M CARR,SAMİM ÖZEN,Yi YAN,Mohammad K HAMEDANİ,FATİH GÜRBÜZ,Eda MENGEN,İHSAN TURAN,Ayça ULUBAY,Gamze AKKUŞ,BİLGİN YÜKSEL,A. Kemal TOPALOĞLU,Etienne LEYGUE | 125–134 |
| Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis | Shan BAO,Jun-Hong CAİ,Shu-Ying YANG,Yongchao REN,Tian FENG,Tianbo JİN,Zhuo-Ri Lİ | 135–143 |
| Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature | Kenan DELİL,HALİL GÜRHAN KARABULUT,BÜLENT HACIHAMDİOĞLU,ZEYNEP ŞIKLAR,MERİH BERBEROĞLU,Gönül ÖCAL,Ajlan TÜKÜN,HATİCE ILGIN RUHİ | 144–149 |
| Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto's Thyroiditis | Pınar İŞGÜVEN,Yasemin GÜNDÜZ,Mukaddes KILIÇ | 150–156 |
| Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto's Thyroiditis | Yasemin GÜNDÜZ, Pınar İŞGÜVEN, Mukaddes KILIÇ | 150–156 |
| 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 GUTİÉRREZ-REPİSO,Icíar GARCÍA-ESCOBAR,Antonio BONİLLO-PERALES | 157–162 |
| Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism | Mehmet Nuri ÖZBEK,HÜSEYİN DEMİRBİLEK,Rıza Taner BARAN,Ahmet BARAN | 163–169 |
| Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course | CENGİZ KARA,Figen GÜNİNDİ,Gülay Can YILMAZ,HASAN MURAT AYDIN | 170–179 |
| Cellular Trace Element Changes in Type 1 Diabetes Patients | Vahap UĞURLU,Çiğdem BİNAY,ENVER ŞİMŞEK,CENGİZ BAL | 180–186 |
| Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey | Nilgün ÇAYLAN,Başak TEZEL,Sema ÖZBAŞ,Nuran ŞAHİN,Şirin AYDIN,Deniz ACICAN,Bekir KESKİNKILIÇ | 187–191 |
| Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey | İHSAN ESEN,Baran OĞUZ,HEPSEN MİNE SERİN | 192–196 |
| Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism | AYLA GÜVEN,Ayşe Nurcan CEBECİ,Sian ELLARD,Sarah E FLANAGAN | 197–204 |
| A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans | Sema AKÇURİN,DOĞA TÜRKKAHRAMAN,Woo-Young KİM,Erdem DURMAZ,Jae-Gook SHİN,Su-Jun LEE | 205–210 |
| Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height | ŞENAY SAVAŞ ERDEVE,ZEYNEP ŞIKLAR,BÜLENT HACIHAMDİOĞLU,Pınar KOCAAY,EMİNE ÇAMTOSUN,Gönül ÖCAL,MERİH BERBEROĞLU | 211–217 |
| Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency | ERDAL EREN,TUBA EDGÜNLÜ,Emre ASUT,SEVİM KARAKAŞ ÇELİK | 218–223 |
| 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 QİU,Man-Li GUO,Xiao-Juan SHAO | 224–227 |
| Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients | Adrijan SARAJLİJA,Tatjana MİLENKOVİC,Maja DJORDJEVİC,Katarina MİTROVİC,Sladjana TODOROVİC,Bozica KECMAN,Khalid HUSSAIN | 228–231 |
| A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty | Cemil KOÇYİĞİT,Serdar SARITAŞ,GÖNÜL ÇATLI,HÜSEYİN ONAY,BUMİN NURİ DÜNDAR | 232–235 |
| 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 SUWAİDİ,Fakunle IBUKUNOLUWA,Salima ATTİA | 236–240 |
| A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient | Chutintorn SRİPHRAPRADANG,Yotsapon THEWJİTCHAROEN,Suwannee CHANPRASERTYOTHİN,Soontaree NAKASATİEN,Thep HİMATHONGKAM,Objoon TRACHOO | 241–245 |
| A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome | Nusrat KHAN,Waleed DANDAN,Noura Al HASSANİ,Suha HADİ | 246–249 |
| 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,Mara De AMİCİ,Matteo VANDONİ,Michela ALBANESİ,Gloria PELİZZO | 250–256 |