The use of ADAMTS13 activity, platelet count, and serum creatinine to differentiate acquired thrombotic thrombocytopenic purpura from other thrombotic microangiopathies
Author:
Affiliation:
1. Division of Hematology; Department of Internal Medicine; Ohio State University; Columbus; OH; USA
2. Department of Pathology; Ohio State University; Columbus; OH; USA
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2012.09032.x/fullpdf
Reference10 articles.
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2. Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement;Coppo;Medicine (Baltimore),2004
3. Evidence for a role of anti-ADAMTS13 autoantibodies despite normal ADAMTS13 activity in recurrent thrombotic thrombocytopenic purpura;Froehlich-Zahnd;Haematologica,2011
4. Survival and relapse in patients with thrombotic thrombocytopenic purpura;Hovinga;Blood,2010
5. Safety & efficacy of eculizumab in aHUS patients resistant to plasma therapy: interim analysis from a phase II trial;Legendre;Journal of the American Society of Nephrology,2010
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