Factor VIII-Mediated Global Hemostasis in the Absence of von Willebrand Factor

Author:

Takeyama Masahiro,Kasuda Shogo,Sakurai Yoshihiko,Shima Midori,Takeda Tomohiro,Omura Shoko,Naka Hiroyuki,Yoshioka Akira

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference27 articles.

1. Sadler JE. A revised classification of von Willebrand disease: for the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost. 1994;71:520-525.

2. Hoffman M, Monroe DM 3rd. A cell-based model of hemostasis. Thromb Haemost. 2001;85:958-965.

3. Mannucci PM, Tamaro G, Narchi G, et al. Life-threatening reaction to factor VIII concentrate in a patient with severe von Willebrand disease and alloantibodies to von Willebrand factor. Eur J Haematol. 1987;39:467-470.

4. Bergamaschini L, Mannucci PM, Federici AB, Coppola R, Guzzoni S, Agostoni A. Posttransfusion anaphylactic reactions in a patient with severe von Willebrand disease: role of complement and alloantibodies to von Willebrand factor. J Lab Clin Med. 1995;125:348-355.

5. Boyer-Neumann C, Dreyfus M, Wolf M, Veyradier A, Meyer D. Multi-therapeutic approach to manage delivery in an alloimmunized patient with type 3 von Willebrand disease. J Thromb Haemost. 2003;1:190-192.

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