Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study-Reference-Cited by-同舟云学术

Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study

Published:2009-08 Issue:8 Volume:7 Page:1304-1312
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:

Author:

EIKENBOOM J.,HILBERT L,RIBBA A. S.,HOMMAIS A.,HABART D.,MESSENGER S.,AL-BUHAIRAN A.,GUILLIATT A.,LESTER W.,MAZURIER C.,MEYER D.,FRESSINAUD E.,BUDDE U.,WILL K.,SCHNEPPENHEIM R.,OBSER T.,MARGGRAF O.,ECKERT E.,CASTAMAN G.,RODEGHIERO F.,FEDERICI A. B.,BATLLE J.,GOUDEMAND J.,INGERSLEV J.,LETHAGEN S.,HILL F.,PEAKE I.,GOODEVE A.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2009.03486.x/fullpdf

Reference30 articles.

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3. Provisional criteria for the diagnosis of VWD type 1;Sadler;J Thromb Haemost,2005

4. Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function;Meyer;Best Pract Res Clin Haematol,2001

5. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology;Eikenboom;Best Pract Res Clin Haematol,2001

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