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Report on the workshop: Von Willebrand factor and thrombotic thrombocytopenic purpura

✍ Scribed by Joel L. Moake; J. Evan Sadler; Pier Mannucci; Pankaj Ganguly


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
34 KB
Volume
68
Category
Article
ISSN
0361-8609

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## Abstract Decreased von Willebrand factor (VWF)‐cleaving protease activity (<5%) has been implicated in patients with congenital thrombotic thrombocytopenic purpura–hemolytic uremic syndrome (Upshaw‐Schulman syndrome) and associated with mutations within the __ADAMTS13__ gene. In this report, we

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