Complement factor H mutations are present in ADAMTS13-deficient, ticlopidine-associated thrombotic microangiopathies
Author:
Affiliation:
1. Division of Hematology-Oncology, Weill Cornell Medical College, New York, NY
2. Carver College of Medicine, University of Iowa, Iowa City, IA
3. Pennsylvania State University, University Park, PA
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/121/19/4012/1218719/4012.pdf
Reference12 articles.
1. Thrombotic thrombocytopenic purpura associated with ticlopidine in the setting of coronary artery stents and stroke prevention.;Bennett;Arch Intern Med,1999
2. Thrombotic thrombocytopenic purpura associated with ticlopidine. A review of 60 cases.;Bennett;Ann Intern Med,1998
3. Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura.;Tsai;Ann Intern Med,2000
4. A new name in thrombosis, ADAMTS13.;Sadler;Proc Natl Acad Sci USA,2002
5. Thienopyridine-linked thrombotic microangiopathy: association with endothelial cell apoptosis and activation of MAP kinase signalling cascades.;Mauro;Br J Haematol,2004
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