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dc.contributor.authorKaraman, S
dc.contributor.authorZulfikar, B
dc.contributor.authorKoc, B
dc.contributor.authorGenc, S
dc.contributor.authorKarakas, Z
dc.contributor.authorAkkaya, Emre
dc.contributor.authorOmer, B
dc.contributor.authorHatiboglu, S
dc.contributor.authorUnuvar, A
dc.date.accessioned2021-03-05T15:19:41Z
dc.date.available2021-03-05T15:19:41Z
dc.date.issued2020
dc.identifier.citationAkkaya E., Hatiboglu S., Koc B., Genc S., Unuvar A., Karaman S., Omer B., Karakas Z., Zulfikar B., "Evaluation of Chromogenic Factor VIII Assay Compared with One-Stage Clotting Assay", CLINICAL LABORATORY, cilt.66, ss.1937-1943, 2020
dc.identifier.issn1433-6510
dc.identifier.otherav_bb5dad8f-535f-4e19-9a44-234e42b2bc78
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/124573
dc.identifier.urihttps://doi.org/10.7754/clin.lab.2020.191145
dc.description.abstractBackground: Congenital factor VIII (FVIII) deficiency causes hemophilia A due to different types of defects in the FVIII gene. Although the chromogenic measurement is the reference method and shows less variability, a one-stage assay is the most commonly preferred method for measurement of FVIII. In this study, we aimed to evaluate the analytical performances of chromogenic and one-stage assays, and compare the results prior to introduction of newly developed extended half-life recombinant FVIII products.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTIBBİ LABORATUVAR TEKNOLOJİSİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectHealth Sciences
dc.subjectMedical Laboratory Technology
dc.titleEvaluation of Chromogenic Factor VIII Assay Compared with One-Stage Clotting Assay
dc.typeMakale
dc.relation.journalCLINICAL LABORATORY
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Temel Tıp Bilimleri Bölümü
dc.identifier.volume66
dc.identifier.issue10
dc.identifier.startpage1937
dc.identifier.endpage1943
dc.contributor.firstauthorID2273498


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