Clinical application of the chromogenic assay of factor VIII in haemophilia A, and different variants of von Willebrand's disease
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1986.tb02636.x/fullpdf
Reference11 articles.
1. Assay of factor VIII:C with a chromogenic substrate;Rosén;Scand J Haematol,1984
2. Clinical application of a chromogenic substrate method for determination of factor VIII activity;Rosén;Thrombos Haemostas,1985
3. Inheritable molecular variants of moderate and mild hemophilia A;Ljung;Acta Med Scand,1981
4. In vivo recovery of factor VIII: A comparison of one-stage and two-stage assay methods;Nilsson;Thrombos Haemostas,1979
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1. Haemophilia A and von Willebrand’s disease;Haemophilia;2010-06-22
2. DDAVP-induced enhancement of platelet retention: Its dependence on platelet-von Willebrand Factor and the platelet receptor GP IIb/IIIa;European Journal of Haematology;2009-04-24
3. von Willebrand's disease;European Journal of Haematology;2009-04-24
4. Cofactors V and VIII after endotoxin administration to human volunteers;Thrombosis Research;1995-12
5. The administration of desmopressin by nasal spray: a dose-determination study in patients with mild haemophilia A or von Willebrand's disease;Haemophilia;1995-04
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