Manuscripts (not published)
The relationship between maternal gestational impaired glucose tolerance with the risk of large for gestational age infants: A meta-analysis of 14 studies
Li Li, Hai-Qing Wang, Han-Lin Lai, Yi Li, Qi-Fei Liu, Shuang Hu, Li Li
DOI : 10.4274/jcrpe.2583
Abstract
(Accept Date:2016-02-01 12:02:41)
Gonadoblastoma and papillary tubal hyperplasia in ovotesticular syndrome
Enver Şimşek, Çiğdem Binay, Meliha Demiral, Baran Tokar, Sare Kabukcuoglu, Melek Üstün
DOI : 10.4274/jcrpe.2705
Abstract
(Accept Date:2016-02-01 11:58:24)
Comparison of bone mineral density in adolescent girls with the diagnosis of hypogonadotropic hypogonadism and hypergonadotropic hypogonadism
huseyin demirbilek, Mehmet Nuri Özbek, Huseyin Demirbilek, Riza Taner Baran, Ahmet Baran
DOI : 10.4274/jcrpe.2228
Abstract
(Accept Date:2016-01-26 16:44:04)
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
Abstract
(Accept Date:2016-01-25 10:52:08)
Neonatal Thyroid Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey
Nilgun Caylan, Basak Tezel, Sema Ozbas, Nuran Sahin, Sirin Aydin, Acican Deniz, Bekir Keskinkilic
DOI : 10.4274/jcrpe.2526
Abstract
(Accept Date:2016-01-25 10:50:29)
A NOVEL MUTATION IN HUMAN ANDROGEN RECEPTOR GENE CAUSING PARTIAL ANDROGEN INSENSITIVITY SYNDROME IN A PATIENT PRESENTING WITH GYNECOMASTIA AT PUBERTY
Serdar Saritas, Cemil Kocyigit, Gonul Catli, Huseyin Onay, Bumin Nuri Dundar
DOI : 10.4274/jcrpe.2637
Abstract
(Accept Date:2016-01-23 17:35:54)
A novel null mutation in P450 aromatase gene (CYP19A1) associated with the development of hypoplastic ovaries in humans
Su-Jun Lee, Sema Akcurin, Doga Turkkahraman, Woo-Young Kim, Erdem Durmaz, Jae-Gook Shin
DOI : 10.4274/jcrpe.2761
Abstract
(Accept Date:2016-01-23 17:35:04)
Cellular Trace Element Changes in Cases with Type 1 Diabetes Treated by Intensive Insulin
Cigdem Binay, Vahap Ugurlu, Enver Simsek, Cengiz Bal
DOI : 10.4274/jcrpe.2449
Abstract
(Accept Date:2016-01-16 18:15:56)
Phenotype, sex of rearing, gender re-assignment and response to medical treatment in extended family with a novel mutation in the SRD5A2 gene
Asma Deeb, Hana Al Suwaidi, Fakunle Ibukunoluwa, Attia Salima
DOI : 10.4274/jcrpe.2782
Abstract
(Accept Date:2016-01-16 18:13:11)
Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
Erdal Eren, Tuba Edgunlu, Emre Asut, Sevim Karakas Celik
DOI : 10.4274/jcrpe.2495
Abstract
(Accept Date:2016-01-12 20:46:34)
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
Abstract
(Accept Date:2016-01-12 20:43:47)
Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto’s Thyroiditis
Pınar İşgüven, İşgüven Pınar, Gündüz Yasemin, Kılıç Mukaddes
DOI : 10.4274/jcrpe.2145
Abstract
(Accept Date:2016-01-06 21:21:54)
A newly-discovered mutation in the RFX6 gene of the rare Mitchell-Riley Syndrome
Nusrat Khan, Suha Hadi, Noura Al Hassani, Waleed Dandan
DOI : 10.4274/jcrpe.2387
Abstract
(Accept Date:2016-01-06 21:16:51)
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 Ángeles Vázquez-López, Eduardo García-Fuentes, Rafael Galera-Martínez, Carolina Gutiérrez-Repiso, Icíar García-Escobar, Antonio Bonillo-Perales
DOI : 10.4274/jcrpe.2687
Abstract
(Accept Date:2015-12-30 01:19:56)
GnRH Analogue Treatment in Females with Early Puberty: No Effect on Final Height
Senay Savas-Erdeve, Zeynep Siklar , Bulent Hacihamdioglu, Pinar Kocaay, Emine Camtosun, Gonul Ocal, Merih Berberoglu
DOI : 10.4274/jcrpe.2356
Abstract
(Accept Date:2015-12-27 17:42:10)
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
Abstract
(Accept Date:2015-12-20 20:45:40)
Clinical, genetic characteristics, management and long-term follow up of Turkish patients with congenital hyperinsulinism
Ayla Güven, Ayla Guven, Ayşe Nurcan Cebeci, Sian Ellard, Sarah E Flanagan
DOI : 10.4274/jcrpe.2408
Abstract
(Accept Date:2015-12-20 20:42:52)
Association of DENND1A gene polymorphisms with polycystic ovary syndrome: a meta-analysis
Zhuo-ri Li, Bao Shan, Cai Jun-hong, Yang Shu-Ying, Ren Yongchao, Feng Tian, Jin Tianbo, Li Zhuo-Ri
DOI : 10.4274/jcrpe.2259
Abstract
(Accept Date:2015-12-18 08:14:51)
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
Abstract
(Accept Date:2015-12-10 23:21:36)
MENSTRUAL CHARACTERISTICS OF PUBERTAL ADOLESCENT GIRLS: A QUESTIONNAIRE BASED STUDY IN TURKEY
ihsan esen, Ihsan Esen, Baran Oguz, Hepsen Mine Serin
DOI : 10.4274/jcrpe.2026
Abstract
(Accept Date:2015-11-30 09:35:24)
Novel c.554+5C>T Mutation in the DUOXA2 gene Combinated with p.R885Q Mutation in the DUOX2 Gene Causes Congenital Hypothyroidism
Shao-Gang Ma, Xiao Zheng, Ya-Li Qiu, Man-Li Guo, Xiao-Juan Shao
DOI : 10.4274/jcrpe.2380
Abstract
(Accept Date:2015-11-15 18:13:50)
Maternal Obesity and its Short and Long Term Maternal and Infantile Effects
LEVENT KORKMAZ, Levent Korkmaz, Osman Bastug, Selim Kurtoglu
DOI : 10.4274/jcrpe.2127
Abstract
(Accept Date:2015-07-29 20:24:04)

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