The aptamer ARC1779 blocks von Willebrand factor-dependent platelet function in patients with thrombotic thrombocytopenic purpura ex vivo-Reference-Cited by-同舟云学术

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The aptamer ARC1779 blocks von Willebrand factor-dependent platelet function in patients with thrombotic thrombocytopenic purpura ex vivo

Published:2010-01-08 Issue:5 Volume:50 Page:1079-1087
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:

Author:

Mayr Florian B.,Knöbl Paul,Jilma Bernd,Siller-Matula Jolanta M.,Wagner Patricia G.,Schaub Robert G.,Gilbert James C.,Jilma-Stohlawetz Petra

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2009.02554.x/fullpdf

Reference36 articles.

1. Thrombotic thrombocytopenic purpura: aetiology, pathophysiology and treatment;Murrin;Blood Rev,2006

2. Von Willebrand factor and thrombosis;Franchini;Ann Hematol,2006

3. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura;Sadler;Blood,2008

4. Thrombotic thrombocytopenic purpura in humans and mice;Desch;Arterioscler Thromb Vasc Biol,2007

5. Unusually large plasma factor VIII: von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura;Moake;N Engl J Med,1982

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