Complement activation in thrombotic microangiopathies
Author:
Affiliation:
1. Section of Benign Hematology; Division of Internal Medicine; University of Texas M.D. Anderson Cancer Center; Houston; Texas; USA
2. Department of Bioengineering; Rice University; Houston; Texas; USA
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12112/fullpdf
Reference10 articles.
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3. Atypical hemolytic uremic syndrome;Kavanagh;Current Opinion in Hematology,2010
4. Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura;Noris;Journal of American Society of Nephrology,1999
5. Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement;Noris;Journal of American Society of Nephrology,2005
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