Loss of von Willebrand factor high-molecular-weight multimers at acute phase is associated with detectable anti-ADAMTS13 IgG and neurological symptoms in acquired thrombotic thrombocytopenic purpura
Author:
Funder
AP-HP
Publisher
Elsevier BV
Subject
Hematology
Reference19 articles.
1. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura;Sadler;Blood,2008
2. Von Willebrand factor-cleaving protease in thrombotic thrombocytopenis purpura and the hemolytic-uremic syndrome;Furlan;N. Engl. J. Med.,1998
3. ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission;Peyvandi;Haematologica,2008
4. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura;Levy;Nature,2001
5. Antibodies to Von Willebrand factor-cleaving protease in acute TTP;Tsai;N. Engl. J. Med.,1998
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