Atıf İçin Kopyala
Akkaya E., Hatiboglu S., Koc B., Genc S., Unuvar A., Karaman S., ...Daha Fazla
CLINICAL LABORATORY, cilt.66, sa.10, ss.1937-1943, 2020 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
66
Sayı:
10
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Basım Tarihi:
2020
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Doi Numarası:
10.7754/clin.lab.2020.191145
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Dergi Adı:
CLINICAL LABORATORY
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, MEDLINE
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Sayfa Sayıları:
ss.1937-1943
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Anahtar Kelimeler:
plasma FVIII activity, hemophilia A, one-stage assay, chromogenic assay, method comparison, MILD HEMOPHILIA-A, FVIII-C ASSAY, DISCREPANCY, MUTATIONS, THROMBIN, STANDARDIZATION, INACTIVATION, COAGULATION, VALIDATION, PHENOTYPE
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İstanbul Üniversitesi Adresli:
Evet
Özet
Background: 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.