RÜYA ÇOLAK
PERSONAL INFORMATION: | Sex: Female Date of Birth and city: 27/04/1982-İzmir Marital Status: Married, mother of 2 children Nationality: Turkish |
EDUCATION: | FellowshipS.B.Ü. İzmir Dr. Behcet Uz Children's Hospital, Neonatology 06/2015-06/2018 Speciality Tepecik Education And Reserch Hospital, Pediatrics 01/2009-04/2013 University Ege University Faculty of Medicine 09/2000-07/2007 High School Buca Anatolian High School 09/1993-06/2000 |
WORK EXPERIENCE: | - Van Bahçesaray Public Hospital, General Medicine, 2007-2008
- Tepecik Traning and Research Hospital, Pediatrician, 2009-2013
- Muş Public Hospital, Pediatrician, 2013-2015
- S.B.Ü. İzmir Dr. Behcet Uz Children's Hospital, Fellowship in Neonatology, 2015-temmuz 2018
- S.B.Ü. İzmir Dr. Behcet Uz Children's Hospital,Neonatologyst, 09.2018-now
|
LANGUAGE SKILLS: | English Reading: Advanced, Writing: Good, Speaking: Good French Reading: Good, Writing: Good, Speaking: Intermediate |
| |
Articles Published in International Refereed Journals:
- Kanık A, Kasap-Demir B, Ateşli R, Eliaçık K, Yavaşcan O, Helvacı M. A Novel OCRL 1 Gene Mutation İn a Turkish Child With Lowe Syndrome. Turk J Pediatr. 2013 Jan-Feb;55(1):82-5.
- Halicioglu O, Akman SA, Tatar B, Atesli R, Kose S. Hepatitis A Seroprevalence İn Children And Adolescents Aged 1-18 Years Among A Low Socioeconomic Population İn İzmir, Turkey. Travel Med Infect Dis. 2012 Jan;10(1):43-7. Doi: 10.1016/J.Tmaid.2012.01.001. Epub 2012 Jan 20.
- Çolak R, Özdemir SA, Ergon EY, Kağnıcı M, Çalkavur Ş. A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: C. 734A> C. Balkan medical journal,2017,34(6), 580.
Articles Published in National Journals:
- Çolak R, Çoban K, Çelik K, Yangın Ergon E, Alkan Özdemir S, Olukman Ö, Çalkavur Ş. Doğum yaralanmaları: Klinik bulgular ile maternal, fetal ve obstetrik risk faktörleri. İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2017, 7(1), 53-59.
- Ergon EY, Özdemir SA, Çolak R, Çelik K, Olukman Ö, Çalkavur Ş. A Newborn Case of “c” Subgroup Mismatch Presenting with Severe Hemolysis and Anemia. Journal Of Pedıatrıc Research, 2017, 4(4), 249-252.
- Altuğ Demirol H, Olukman Ö, Nalbantoğlu Elmas Ö, Çelik K, Çolak R, Çalkavur Ş. A Neonatal Case of Congenital Hyperinsulinism Due to Homozygous KCNJ11 Gene Mutation. The Journal of Tepecik Education and Research Hospital,2017, 27(2), 163-167.
- Ergon, EY, Acar BH, Çelik K, Çolak R, Özdemir SA, Gözmen Ş K,.Çalkavur Ş. Yenidoğanda İdrar Yolu Enfeksiyonları. Türkiye Çocuk Hastalıkları Dergisi,2017.