An inquiry into the relationship between ABO blood group and thrombotic thrombocytopenic purpura
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1423-0410.2009.01164.x/fullpdf
Reference21 articles.
1. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome;Furlan;N Engl J Med,1998
2. Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion;Tsai;Blood,1996
3. Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease;Furlan;Best Pract Res Clin Haematol,2001
4. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity;Kokame;PNAS,2002
5. ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity;Savasan;Blood,2003
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4. Non-O blood group thrombotic thrombocytopenic purpura patients take longer to recover as measured by number of therapeutic plasma exchanges needed for platelet recovery;Thrombosis Research;2020-01
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