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Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia.
Aydin Koker S, Karapinar TH, Oymak Y, Bianchi P, Fermo E, Gozmen S, Vergin C. Aydin Koker S, et al. Among authors: oymak y. J Pediatr Hematol Oncol. 2018 Oct;40(7):e421-e423. doi: 10.1097/MPH.0000000000001207. J Pediatr Hematol Oncol. 2018. PMID: 29846281
A single center's experience with Candida parapsilosis related long-term central venous access device infections: the port removal decision and its outcomes.
Devrim I, Yaman Y, Demirağ B, Oymak Y, Cartı Ö, Özek G, Tulumoğlu S, Erdem T, Gamze G, Gözmen S, Güneş BT, Bayram N, Vergin C. Devrim I, et al. Among authors: oymak y. Pediatr Hematol Oncol. 2014 Aug;31(5):435-41. doi: 10.3109/08880018.2013.862587. Epub 2014 Jan 2. Pediatr Hematol Oncol. 2014. PMID: 24383767 Clinical Trial.
The effectiveness of tools for monitoring hemophilic arthropathy.
Oymak Y, Yildirim AT, Yaman Y, Gurcinar M, Firat A, Cubuckcu D, Carti O, Ozek G, Vergin RC. Oymak Y, et al. J Pediatr Hematol Oncol. 2015 Mar;37(2):e80-5. doi: 10.1097/MPH.0000000000000210. J Pediatr Hematol Oncol. 2015. PMID: 25000469
Chronic Neutropenia in Childhood: Experience From a Single Center.
Karapinar TH, Oymak Y, Ay Y, Köker SA, Töret E, Hazan F, Vergin C. Karapinar TH, et al. Among authors: oymak y. J Pediatr Hematol Oncol. 2016 Jan;38(1):e35-8. doi: 10.1097/MPH.0000000000000449. J Pediatr Hematol Oncol. 2016. PMID: 26479986
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