Manuscripts (not published)
Vitamin D Deficiency in Pediatric Fracture Patients: prevalence, risk factors, and vitamin D supplementation
Erwin Gorter, E.A. Gorter, W. Oostdijk, A. Felius, P. Krijnen, I.B. Schipper
DOI : 10.4274/jcrpe.3474
Abstract
(Accept Date:2016-08-17 16:43:27)
STOSSTHERAPY IN NUTRITIONAL RICKETS: AN INSIGHT INTO THE SAFETY AND EFFICACY OF TREATMENT
Daipayan Chatterjee, Daipayan Chatterjee, Mathad KS Swamy, Vikas Gupta, Vasu Sharma, Akshat Sharma, Krishti Chatterjee
DOI : 10.4274/jcrpe.3557
Abstract
(Accept Date:2016-08-17 16:41:17)
COMPARISON OF UPDATED WEIGHT AND HEIGHT PERCENTILES WITH THE PREVIOUS REFERENCES PRODUCED THREE YEARS AGO IN 6-17 YEAR OLD CHILDREN IN KAYSERI, TURKEY
Ahmet Öztürk, Gokmen Zararsız, Betul Çiçek, Meda Kondolot, M.Mümtaz Mazıcıoğlu, Ahmet Ozturk, Selim Kurtoglu
DOI : 10.4274/jcrpe.3482
Abstract
(Accept Date:2016-08-08 12:59:48)
Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children and Adolescents
ADNAN AL SHAIKH, ADNAN M. AL SHAIKH, Bahaa Abaalkhail, Ashraf Soliman, Ibrahim Kaddam, Khalid Aseri, Yousef Al Saleh, Ali Al Qarni, Ahmed Al Shuaibi, Waleed Al Tamimi, Abdel Moniem Mukhtar
DOI : 10.4274/jcrpe.3301
Abstract
(Accept Date:2016-07-30 18:17:56)
Testicular Adrenal Rest Tumor In Brothers With Novel Mutation In 3-Beta Hydroxysteroid Dehydrogenase -2 Gene
Ayla Güven, Ayla Güven, Seher Polat
DOI : 10.4274/jcrpe.3306
Abstract
(Accept Date:2016-07-29 09:10:37)
<Pseudohypoparathyroidism Type IA Subclinical Hypothyroidism and Rapid Weight Gain weight As Early Clinical Signs. A clinical Study of 10 Cases.
Simon Kayemba-Kay's, SIMON KAYEMBA-KAY'S, CEDRIC TRIPON, ANNE HERON, PETER HINDMARSH
DOI : 10.4274/jcrpe.2743
Abstract
(Accept Date:2016-07-27 20:38:11)
Clinical and molecular genetic analysis in three children with Wolfram Syndrome: a novel WFS1 mutation (c.2534T>A)
Gamze Celmeli, Gamze Celmeli, Doga Turkkahraman, Yusuf Curek, Jayne Houghton, Sema Akcurin, Iffet Bircan
DOI : 10.4274/jcrpe.2894
Abstract
(Accept Date:2016-07-27 16:38:11)
Lower plasma ghrelin levels are found in women with diabetes-complicated pregnancies
Rita A. Gomez-Diaz, Rita A. Gómez-Díaz, Mónica Patricia Gómez-Medina , Eleazar Ramírez-Soriano, Lucio López-Robles, Carlos A. Aguilar-Salinas, Renata Saucedo , Arturo Zarate, Adán Valladares-Salgado, Niels H. Wacher
DOI : 10.4274/jcrpe.2504
Abstract
(Accept Date:2016-07-19 13:10:23)
Longitudinal Observation in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation of the GNAS Gene
Sezgin Sahin, Sezgin Sahin, Olaf Hiort, Susanne Thiele, Olcay Evliyaoğlu, Beyhan Tüysüz
DOI : 10.4274/jcrpe.3191
Abstract
(Accept Date:2016-07-16 17:39:39)
The first case of vitamin D dependent rickets type 1A from Uzbek population with a novel mutation
Bahar Özcabı, Bahar Özcabı, Feride Tahmiscioğlu Bucak, Sevinç Jaferova, Çiğdem Oruç, Amra Adrovic, Serdar Ceylaner, Oya Ercan, Olcay Evliyaoğlu
DOI : 10.4274/jcrpe.3128
Abstract
(Accept Date:2016-06-28 08:20:29)
A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey
Zehra Yavaş Abalı, Zehra Yavas Abali, Feyza Darendeliler, Olcay Neyzi
DOI : 10.4274/jcrpe.3209
Abstract
(Accept Date:2016-06-25 14:58:13)
NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA IN CHILDHOOD
Nihal Hatipoglu, Selim Kurtoglu, Nihal Hatipoglu
DOI : 10.4274/jcrpe.3378
Abstract
(Accept Date:2016-06-25 14:57:41)
Development and validation of Pediatric Endocrine Knowledge Assessment Questionnaire (PEKAQ): Impact of PEKAQ intervention study
Nidhi Gupta, Nidhi Gupta, Marwan Zidan, Kathleen Moltz, Amita Adhikari, Colleen Buggs-Saxton, Hanaa Zidan, Dania Abushanab, Aida Lteif, Chandra Edwin
DOI : 10.4274/jcrpe.3171
Abstract
(Accept Date:2016-06-22 10:49:45)
The 13C-glucose breath test for insulin resistance assessment in adolescents: comparison with fasting and post-glucose stimulus surrogate markers of insulin resistance
José Navarro-Betancourt, Jorge Maldonado-Hernández , Azucena Martínez-Basila, Alejandra Salas-Fernández , José R Navarro-Betancourt, Mónica I Piña-Aguero , Mariela Bernabe-García
DOI : 10.4274/jcrpe.3260
Abstract
(Accept Date:2016-06-18 12:59:14)
The Role of Osteopontin in the Pathogenesis and Complication of Type 1 Diabetes Mellitus in Children and Adolescents
Mohamed Talat, Mohamed Talat, Laila Sherief, Hosam El-Saadany, Anwar Ahmed, Rabab M. Saleh, Maha sakr
DOI : 10.4274/jcrpe.3082
Abstract
(Accept Date:2016-06-06 21:49:44)
Breast milk iodine concentrations, iodine status and thyroid function of breastfed infants aged 2-4 months and their mothers residing in a South African township
Jennifer Osei, Jennifer Osei, Maria Andersson, Olivia van der Reijden, Susanne Dold, Cornelius Smuts, Jeannine Baumgartner
DOI : 10.4274/jcrpe.2720
Abstract
(Accept Date:2016-05-22 13:24:11)
Influence of obesity on luteinizing hormone secretion during gonadotropin-releasing hormone stimulation tests in girls with central precocious puberty
Hae Sang Lee, Lee Hae Sang, Yoon Jong Seo, Hwang Jin Soon
DOI : 10.4274/jcrpe.3091
Abstract
(Accept Date:2016-05-22 13:22:51)
The p.(Glu809Lys) mutation in the WFS1 gene is associated with the occurrence of the Wolfram-like syndrome-WFSL: a case report
Dagmar Prochazkova, Dagmar Prochazkova, Zuzana Hruba, Petra Konecna, Jarmila Skotakova, Lenka Fajkusova
DOI : 10.4274/jcrpe.3021
Abstract
(Accept Date:2016-05-22 12:58:43)
Association between Common genetic variants of PCOS risk in a Chinese Han population
Tianbo Jin, Sun Ying, Yuan Yi, Yang Hua, Li Jingjie, Feng Tian, Ouyang Yongri, Jin Tianbo, Liu Ming
DOI : 10.4274/jcrpe.2784
Abstract
(Accept Date:2016-05-22 12:57:53)
A NOVEL HOMOZYGOUS MUTATION IN THE KCNJ11 GENE p.F315I OF A NEONATE WITH CONGENITAL HYPERINSULINISM AND SUCCESFUL MANAGEMENT BY SIROLIMUS
Sevim Ünal, Sevim Ünal, Deniz Gonulal, Ahmet Ucaktürk, Betül Siyah Bilgin, Sarah E Flanagan, Fatih Gürbüz, Meltem Tayfun, Selin Elmaoğulları, Aslıhan Araslı, Fatma Demirel, Sian Ellard, Khalid Hussain
DOI : 10.4274/jcrpe.2773
Abstract
(Accept Date:2016-05-10 12:47:33)
Current Status of Childhood Hyperinsulinaemic Hypoglycaemia in Turkey
zeynep şıklar, zeynep şıklar, merih berberoğlu
DOI : 10.4274/jcrpe.2991
Abstract
(Accept Date:2016-05-09 21:56:11)
Wolcott–Rallison syndrome with novel EIF2AK3 gene mutation
Fatih Gürbüz, Fatih Gurbuz, Bilgin Yuksel, Ali Kemal Topaloglu
DOI : 10.4274/jcrpe.3065
Abstract
(Accept Date:2016-05-04 12:20:39)
Novel missense mutation in the CLPP gene causes Perrault Syndrome type-3 in a Turkish family
Fatma dursun, Fatma Dursun, Hussein Sheikh Ali Mohamoud, Noreen Karim, Muhammad Naeem, Musharraf Jelani, Heves Kırmızıbekmez
DOI : 10.4274/jcrpe.2717
Abstract
(Accept Date:2016-04-05 06:25:38)
Complex glycerol kinase deficiency and adrenocortical insufficiency in the neonate
Sabriye Korkut, Sabriye Korkut, Osman Baştuğ, Margarita Raygada, Nihal Hatipoğlu, Selim Kurtoğlu, Mustafa Kendirci, Charalampos Lyssikatos, Constantine A. Stratakis
DOI : 10.4274/jcrpe.2539
Abstract
(Accept Date:2016-03-08 11:16:06)

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