Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults-Reference-Cited by-同舟云学术

Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults

Published:2013-01-10 Issue:4 Volume:8 Page:554-562
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Fremeaux-Bacchi Véronique,Fakhouri Fadi,Garnier Arnaud,Bienaimé Frank,Dragon-Durey Marie-Agnès,Ngo Stéphanie,Moulin Bruno,Servais Aude,Provot François,Rostaing Lionel,Burtey Stéphane,Niaudet Patrick,Deschênes Georges,Lebranchu Yvon,Zuber Julien,Loirat Chantal

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference21 articles.

1. Atypical Hemolytic–Uremic Syndrome

2. Clinical Features of Anti-Factor H Autoantibody–Associated Hemolytic Uremic Syndrome

3. Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

4. A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

5. The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

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