COMPLEMENTing the diagnosis of aHUS
Author:
Affiliation:
1. THE UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/124/11/1699/1468709/1699.pdf
Reference6 articles.
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3. Genetic studies into inherited and sporadic hemolytic uremic syndrome.;Warwicker;Kidney Int,1998
4. Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency.;Józsi;Blood,2008
5. Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome.;Roumenina;Blood,2009
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4. The Alternative Pathway of Complement and the Evolving Clinical-Pathophysiological Spectrum of Atypical Hemolytic Uremic Syndrome;The American Journal of the Medical Sciences;2016-08
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