Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura
Author:
Affiliation:
1. Division of Hematology Albert Einstein College of Medicine Montefiore Medical Center Bronx, NY e‐mail:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1537-2995.2002.00267.x
Reference8 articles.
1. Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome: will recent insight into pathogenesis translate into better treatment?
2. Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
3. Inhibitiors of von Willebrand factor‐cleaving protease in thrombotic thrombocytopenic purpura.;Tsai HM;Clin Lab,2001
4. Von Willebrand Factor and Von Willebrand Factor-Cleaving Metalloprotease Activity in Escherichia coli O157:H7-Associated Hemolytic Uremic Syndrome
5. Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangiopathy
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1. Thrombotic Microangiopathies;Practical Hemostasis and Thrombosis;2016-11-11
2. Von Willebrand Factor Structure and Function;Von Willebrand Disease;2011-03-21
3. Nine Years of Cascade Filtration for Thrombotic Thrombocytopenic Purpura;Therapeutic Apheresis and Dialysis;2004-04
4. Severe deficiency of VWF-cleaving protease (ADAMTS13) activity defines a distinct population of thrombotic microangiopathy patients;Transfusion;2004-02
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