Atypical HUS may become a diagnosis of inclusion
Author:
Affiliation:
1. WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/125/23/3525/1387157/3525.pdf
Reference7 articles.
1. Modified Ham test for atypical hemolytic uremic syndrome.;Gavriilaki;Blood,2015
2. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome.;Legendre;N Engl J Med,2013
3. Biomarkers of terminal complement activation confirm the diagnosis of aHUS and differentiate aHUS from TTP.;Cataland;Blood,2014
4. Dynamics of complement activation in aHUS and how to monitor eculizumab therapy.;Noris;Blood,2014
5. Complement activation patterns in atypical hemolytic uremic syndrome during acute phase and in remission [published online ahead of print July 31, 2014].;Volokhina;Clin Exp Immunol
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1. Atypical hemolytic uremic syndrome in first trimester pregnancy successfully treated with eculizumab;Experimental Hematology & Oncology;2017-01-13
2. The complex differential diagnosis between thrombotic thrombocytopenic purpura and the atypical hemolytic uremic syndrome: Laboratory weapons and their impact on treatment choice and monitoring;Thrombosis Research;2015-11
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