Use of a High-Purity Factor VIII Concentrate (Hemate P) in von Willebrand's Disease
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1423-0410.1989.tb02031.x/fullpdf
Reference23 articles.
1. Factor VIII, a series of homologous oligomers and a complex of two proteins;Mourik;Thromb. Res.,1974
2. Multimeric structure of platelet factor VIII/von Willebrand factor: the presence of larger multimers and their reassociation with thrombin-stimulated platelets;Fernandez;Blood,1982
3. Adhesion of platelets to human artery subendothelium: effect of factor VIII - von Willebrand factor of various multimeric composition;Sixma;Blood,1984
4. Von Willebrand disease;Holmberg;Clin. Haematol.,1985
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2. Production and Clinical Profile of Human Plasma-Derived Von Willebrand Factor;Production of Plasma Proteins for Therapeutic Use;2012-12-14
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4. von Willebrand factor/factor VIII concentrate (Humate-P) for management of elective surgery in adults and children with von Willebrand disease;Haemophilia;2011-04-27
5. Treatment of Von Willebrand Disease: Therapeutic Concentrates;Textbook of Hemophilia;2010-08-13
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