Research article summary (published 20 Oct 2009):

Atypical hemolytic-uremic syndrome.

Full Abstract

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Author information

Author/s: Noris, Marina (M); Remuzzi, Giuseppe (G);

Affiliation: Clinical Research Center for Rare Diseases Aldo e Cele Daccò, Mario Negri Institute for Pharmacological Research, Bergamo, Italy.

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

Journal: The New England journal of medicine (N Engl J Med), published in United States. (Language: eng)

Reference: 2009-Oct; vol 361 (issue 17) : pp 1676-87

Dates: Created 2009/10/22; Completed 2009/10/29;

PMID: 19846853, status: MEDLINE (last retrieval date: 10/29/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Autoantibodies - metabolism Complement Factor H - genetics; immunology Complement Pathway, Alternative - genetics Complement System Proteins - genetics; metabolism Hemolytic-Uremic Syndrome - classification; genetics; therapy Humans

Kidney Glomerulus - pathology Kidney Transplantation Mutation Penetrance Point Mutation Prognosis

Associated Chemicals: Autoantibodies (0) ; complement factor H, human (0) ; Complement Factor H (80295-65-4) ; Complement System Proteins (9007-36-7)

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• The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. 30 Jan 2001
• Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease. 26 Oct 2003
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