Tailored eculizumab regimen for patients with atypical hemolytic uremic syndrome: requirement for comprehensive complement analysis
Author:
Affiliation:
1. Institute of Immunology; University of Heidelberg; Heidelberg Germany
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12639/fullpdf
Reference19 articles.
1. Complement-mediated injury and protection of endothelium: lessons from atypical haemolytic uraemic syndrome;Kerr;Immunobiology,2012
2. STEC-HUS, atypical HUS and TTP are all diseases of complement activation;Noris;Nat Rev Nephrol,2012
3. Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype;Bresin;J Am Soc Nephrol,2013
4. A time for reappraisal of ‘atypical’ hemolytic uremic syndrome: should all patients be treated the same?;Ruebner;Eur J Pediatr,2012
5. Tailored eculizumab therapy in the management of complement factor H-mediated atypical hemolytic uremic syndrome in an adult kidney transplant recipient: a case report;Xie;Transpl Proc,2012
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