Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon?-Reference-Cited by-同舟云学术

Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon?

Published:2012-01-05 Issue:3 Volume:7 Page:417-426
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Kavanagh David,Pappworth Isabel Y.,Anderson Holly,Hayes Christine M.,Moore Iain,Hunze Eva-Maria,Bennaceur Karim,Roversi Pietro,Lea Susan,Strain Lisa,Ward Roy,Plant Nick,Nailescu Corina,Goodship Timothy H. J.,Marchbank Kevin J.

Publisher

American Society of Nephrology (ASN)

Subject

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

Reference49 articles.

1. Complement Regulatory Genes and Hemolytic Uremic Syndromes

2. Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition

3. Heterozygous and Homozygous Factor H Deficiencies Associated with Hemolytic Uremic Syndrome or Membranoproliferative Glomerulonephritis: Report and Genetic Analysis of 16 Cases

4. The molecular basis of familial hemolytic uremic syndrome: Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.;Caprioli;J Am Soc Nephrol,2001

5. Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome

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