Ten years of prophylactic treatment with fresh-frozen plasma in a child with chronic relapsing thrombotic thrombocytopenic purpura as a result of a congenital deficiency of von Willebrand factor-cleaving protease
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.02808.x/fullpdf
Reference10 articles.
1. Deficiency of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura;Furlan;Blood,1997
2. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome;Furlan;New England Journal of Medicine,1998
3. Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura;Furlan;Thrombosis and Haemostasis,1999
4. Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura;Gerritsen;Thrombosis and Haemostasis,1999
5. New strategies in diagnosis and treatment of thrombotic thrombocytopenic purpura: case report and review;Häberle;European Journal of Pediatrics,1999
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