Distal Angiopathy and Atypical Hemolytic Uremic Syndrome: Clinical and Functional Properties of an Anti–Factor H IgAλ Antibody-Reference-Cited by-同舟云学术

Distal Angiopathy and Atypical Hemolytic Uremic Syndrome: Clinical and Functional Properties of an Anti–Factor H IgAλ Antibody

Published:2015-08 Issue:2 Volume:66 Page:331-336
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Rigothier Claire,Delmas Yahsou,Roumenina Lubka T.,Contin-Bordes Cécile,Lepreux Sébastien,Bridoux Frank,Goujon Jean Michel,Bachelet Thomas,Touchard Guy,Frémeaux-Bacchi Véronique,Combe Christian

Publisher

Elsevier BV

Subject

Nephrology

Reference23 articles.

1. A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function;Roumenina;Blood,2012

2. Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome;Roumenina;Blood,2009

3. Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome;Manuelian;J Clin Invest,2003

4. Complement factor H polymorphism in age-related macular degeneration;Klein;Science,2005

5. Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency;Jozsi;Blood,2008

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3. How I diagnose and treat atypical hemolytic uremic syndrome;Blood;2023-03-02

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