Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign?-Reference-Cited by-同舟云学术

Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign?

Published:2014-03-20 Issue:9 Volume:25 Page:2053-2065
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Marinozzi Maria Chiara,Vergoz Laura,Rybkine Tania,Ngo Stephanie,Bettoni Serena,Pashov Anastas,Cayla Mathieu,Tabarin Fanny,Jablonski Mathieu,Hue Christophe,Smith Richard J.,Noris Marina,Halbwachs-Mecarelli Lise,Donadelli Roberta,Fremeaux-Bacchi Veronique,Roumenina Lubka T.

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference46 articles.

1. Atypical Hemolytic–Uremic Syndrome

2. Alternative complement pathway assessment in patients with atypical HUS

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

4. Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic–Uremic Syndrome

5. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

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