| 1. | Cover
Pages I - XI
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| EDITOR’S NOTE |
| 2. | Editor’s Note
Feyza Darendeliler
Page VIII
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| REVIEW |
| 3. | Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects
Levent Korkmaz, Osman Baştuğ, Selim Kurtoğlu
Pages 114 - 124
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| ORIGINAL ARTICLE |
| 4. | Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1
Leman Damla Kotan, Charlton Cooper, Şükran Darcan, Ian M. Carr, Samim Özen, Yi Yan, Mohammad K. Hamedani, Fatih Gürbüz, Eda Mengen, İhsan Turan, Ayça Ulubay, Gamze Akkuş, Bilgin Yüksel, A. Kemal Topaloğlu, Etienne Leygue
doi: 10.4274/jcrpe.3248 Pages 125 - 134
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| 5. | Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis
Shan Bao, Jun-Hong Cai, Shu-Ying Yang, Yongchao Ren, Tian Feng, Tianbo Jin, Zhuo-Ri Li
doi: 10.4274/jcrpe.2259 Pages 135 - 143
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| 6. | Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature
Kenan Delil, Halil Gürhan Karabulut, Bülent Hacıhamdioğlu, Zeynep Şıklar, Merih Berberoğlu, Gönül Öçal, Ajlan Tükün, Hatice Ilgın Ruhi
doi: 10.4274/jcrpe.2307 Pages 144 - 149
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| 7. | Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto’s Thyroiditis
Pınar İşgüven, Yasemin Gündüz, Mukaddes Kılıç
doi: 10.4274/jcrpe.2145 Pages 150 - 156
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| 8. | 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
doi: 10.4274/jcrpe.2687 Pages 157 - 162
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| 9. | Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism
Mehmet Nuri Özbek, Hüseyin Demirbilek, Rıza Taner Baran, Ahmet Baran
doi: 10.4274/jcrpe.2228 Pages 163 - 169
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| 10. | Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course
Cengiz Kara, Figen Günindi, Gülay Can Yılmaz, Murat Aydın
doi: 10.4274/jcrpe.2345 Pages 170 - 179
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| 11. | Cellular Trace Element Changes in Type 1 Diabetes Patients
Vahap Uğurlu, Çiğdem Binay, Enver Şimşek, Cengiz Bal
doi: 10.4274/jcrpe.2449 Pages 180 - 186
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| 12. | Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey
Nilgün Çaylan, Başak Tezel, Sema Özbaş, Nuran Şahin, Şirin Aydın, Deniz Acıcan, Bekir Keskinkılıç
doi: 10.4274/jcrpe.2526 Pages 187 - 191
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| 13. | Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey
İhsan Esen, Baran Oğuz, Hepsen Mine Serin
doi: 10.4274/jcrpe.2026 Pages 192 - 196
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| 14. | Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism
Ayla Güven, Ayşe Nurcan Cebeci, Sian Ellard, Sarah E. Flanagan
doi: 10.4274/jcrpe.2408 Pages 197 - 204
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| 15. | 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
doi: 10.4274/jcrpe.2761 Pages 205 - 210
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| 16. | Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height
Şenay Savaş-Erdeve, Zeynep Şıklar, Bülent Hacıhamdioğlu, Pınar Kocaay, Emine Çamtosun, Gönül Öcal, Merih Berberoğlu
doi: 10.4274/jcrpe.2356 Pages 211 - 217
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| 17. | Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
Erdal Eren, Tuba Edgünlü, Emre Asut, Sevim Karakaş Çelik
doi: 10.4274/jcrpe.2495 Pages 218 - 223
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| CASE REPORT |
| 18. | A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism
doi: 10.4274/jcrpe.2380 Pages 224 - 227
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| 19. | Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients
Adrijan Sarajlija, Tatjana Milenkovic, Maja Djordjevic, Katarina Mitrovic, Sladjana Todorovic, Bozica Kecman, Khalid Hussain
doi: 10.4274/jcrpe.2436 Pages 228 - 231
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| 20. | 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, Hüseyin Onay, Bumin Nuri Dündar
doi: 10.4274/jcrpe.2637 Pages 232 - 235
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| 21. | 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, Salima Attia
doi: 10.4274/jcrpe.2782 Pages 236 - 240
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| 22. | 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, Objoon Trachoo
doi: 10.4274/jcrpe.2503 Pages 241 - 245
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| 23. | A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome
Nusrat Khan, Waleed Dandan, Noura Al Hassani, Suha Hadi
doi: 10.4274/jcrpe.2387 Pages 246 - 249
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| 24. | 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 Amici, Matteo Vandoni, Michela Albanesi, Gloria Pelizzo
doi: 10.4274/jcrpe.2283 Pages 250 - 256
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