Factor VIII:C and VIII:CAg Response in Patients with Haemophilia A and von Willebrand's Disease after Administration of Different Factor VIII Concentrates or Plasma
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1981.tb02688.x/fullpdf
Reference33 articles.
1. J.P. Allain, F. Verroust, and J.P. Soulier (1979 ) Comparative in vitro and in vivo study of various factor VIII preparations. (Abstract). VIIth International Congress of Thrombosis and Haemostasis, London, p.65 .
2. T.W. Barrowcliffe, G. Kemball-Cook, G. Morris, J.C. Holt, and I.R. Peake (1979 ) Factor VIII- related activities in therapeutic concentrates. (Abstract). Vllth International Congress on Thrombosis and Haemostasis, London, p.71 .
3. Immunologic Studies in von Willebrand's Disease
4. Antihemophilic factor concentrate therapy in von Willebrand disease. Dissociation of bleeding-time factor and ristocetin-cofactor activities
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1. Long-term high dose factor VIII treatment of 3 haemophiliacs with factor VIII inhibitor;Scandinavian Journal of Haematology;2009-04-24
2. FACTOR VIII RELATED ACTIVITIES IN CONCENTRATES;Scandinavian Journal of Haematology;2009-04-24
3. IN VIVO RECOVERY OF FVIII:C IN HEMOPHILIC PATIENTS;Scandinavian Journal of Haematology;2009-04-24
4. Calculations of Factor VIII in vivo Recovery and Half-life;Scandinavian Journal of Haematology;2009-04-24
5. North American Study of Factor VIII Concentrate Potency;Scandinavian Journal of Haematology;2009-04-24
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