ISSN: 1308-5727 | E-ISSN: 1308-5735
Volume : 8 Issue : 2 Year : 2023
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Abstracting & Indexing
Turkish Society for Pediatric Endocrinology and Diabetes
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY - J Clin Res Pediatr Endocrinol: 8 (2)
Volume: 8  Issue: 2 - 2016
1.Cover

Pages I - XI

EDITOR’S NOTE
2.Editor’s Note
Feyza Darendeliler
Page VIII

REVIEW
3.Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects
Levent Korkmaz, Osman Baştuğ, Selim Kurtoğlu
Pages 114 - 124

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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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