Eculizumab in the treatment of refractory idiopathic thrombotic thrombocytopenic purpura
Author:
Affiliation:
1. Division of Hematology-Oncology; New York Presbyterian Hospital-Weill Cornell Medical College; New York; NY; USA
2. Department of Pathology; New York Presbyterian Hospital-Weill Cornell Medical College; New York; NY; USA
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2012.09084.x/fullpdf
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3. Complement inhibitor eculizumab in atypical hemolytic uremic syndrome;Mache;Clinical Journal of the American Society of Nephrology,2009
4. Thrombotic thrombocytopenic purpura and sporadic hemolytic-uremic syndrome plasmas induce apoptosis in restricted lineages of human microvascular endothelial cells;Mitra;Blood,1997
5. Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement;Noris;Journal of the American Society of Nephrology,2005
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