Deficiency of ADAMTS-13 in thrombotic and thrombocytopenic purpura
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1538-7836.2003.t01-1-00377.x/fullpdf
Reference11 articles.
1. Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic purpura? No
2. von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome
3. High titers of inhibitors of von Willebrand factor-cleaving metalloproteinase in a fatal case of acute thrombotic thrombocytopenic purpura
4. Von Willebrand Factor and Von Willebrand Factor-Cleaving Metalloprotease Activity in Escherichia coli O157:H7-Associated Hemolytic Uremic Syndrome
5. Subunit composition of plasma von Willebrand factor multimers: Evidence for a non-proteolytic mechanism resulting in apparent increase in proteolytic fragments
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3. Thrombotic Thrombocytopenic Purpura in a ChildWithSystemic Lupus Erythematosus;Journal of Pediatric Hematology/Oncology;2011-04
4. A splice variant of ADAMTS13 is expressed in human hepatic stellate cells and cancerous tissues;Thrombosis and Haemostasis;2010
5. Blood coagulation and its regulation by anticoagulant pathways: genetic pathogenesis of bleeding and thrombotic diseases;Journal of Internal Medicine;2005-03
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