Potency and mass of factor VIII in FVIII products
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2008.01826.x/fullpdf
Reference40 articles.
1. Genetic basis of hemophilia A;Gitschier;Thromb Haemost,1991
2. A concentrate of human antihaemophilic factor - its use in six cases of haemophilia;Kekwick;Lancet,1957
3. Treatment of hemophilia B with a new clotting-factor concentrate;Hoag;N Engl J Med,1969
4. Hepatitis, epidemiology and liver function in hemophiliacs in Sweden;Schulman;Acta Med Scand,1984
5. Factor IX concentrates for clinical use;Thompson;Semin Thromb Hemost,1993
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2. Differences in wild-type– and R338L-tenase complex formation are at the root of R338L-factor IX assay discrepancies;Blood Advances;2023-02-06
3. Characterization of protein unable to bind von Willebrand factor in recombinant factor VIII products;Journal of Thrombosis and Haemostasis;2021-02-24
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