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Thromb Haemost 1975; 34(01): 306-308
DOI: 10.1055/s-0038-1651343
DOI: 10.1055/s-0038-1651343
Letter to the Editor
A Method for Assaying von Willebrand Factor (Ristocetin Cofactor)
Further Information
Publication History
Publication Date:
02 July 2018 (online)
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References
- 1 Allain J. P, Cooper H. A, Wagner R. H, and Brinkhous K. M. 1975; Platelets fixed with paraformaldehyde: a new reagent for assay of von Willebrand factor and platelet aggregating factor. Journal of Laboratory and Clinical Medicine 85: 318.
- 2 Grant P. A, McPherson J, and Zucker M. B. 1975; Inhibition and reversal by ADP of human platelet aggregation induced by ristocetin or porcine von Willebrand factor. Federation Proceedings 34: 222.
- 3 Howard M. A, and Firkin B. G. 1971; Ristocetin - a new tool in the investigation of platelet aggregation. Thrombosis et Diathesis Haemorrhagica 26: 362.
- 4 Kirby E. P, and Mills D. C. B. 1975 The interaction of bovine Factor VIII with human platelets. Journal of Clinical Investigation. In press.
- 5 Olson J. D, Brockway W. J, Fass D. N, Magnuson M. A, and Bowie E. J. W. 1975; Evaluation of ristocetin-Willebrand factor assay and ristocetin-induced platelet aggregation. American Journal of Clinical Pathology 63: 210.
- 6 Meyer D, Jenkins C. S. P, Dreyfus M. D, Fressinaud E, and Larrieu M.-J. 1974; Willebrand factor and ristocetin. II. Relationship between Willebrand factor, Willebrand antigen and factor VIII activity. British Journal of Haematology 28: 579.
- 7 Stibbe J, and Kirby E. P. 1975 a Inhibition of ristocetin-induced platelet aggregation by Haemaccel ® and fibrinogen. Abstract Vth International Congress of the International Society on Thrombosis and Haemostasis, Paris.
- 8 Stibbe J, and Kirby E. P. 1975 b Influence of fibrinogen, albumin and Haemaccel on ristocetin-induced platelet aggregation; its relevance to the quantitative measurement of the ristocetin cofactor. In preparation.
- 9 Weiss H. J, Hoyer L. W, Rickles F. R, Varma A, and Rogers J. 1973; Quantitative assay of plasma factor deficient in von Willebrand’s disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content. Journal of Clinical Investigation 52: 2708.
- 10 Zimmerman T. S, Ratnoff O. D, and Powell A. E. 1971; Immunologic differentiation of classic hemophilia (factor VIII deficiency) and von Willebrand’s disease. Journal of Clinical Investigation 50: 244.