Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome (Q33390761)

26 July 2017

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title

Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome (English)

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26 July 2017

Pilar Sánchez-Corral

1

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26 July 2017

Marta Melgosa

series ordinal

2

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26 July 2017

language of work or name

English

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publication date

14 July 2010

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British Journal of Haematology

26 July 2017

published in

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26 July 2017

volume

150

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26 July 2017

issue

5

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26 July 2017

page(s)

529-542

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A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity

26 July 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1365-2141.2010.08295.X

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2010.08295.X

Lack of association between polymorphisms in C4b-binding protein and atypical haemolytic uraemic syndrome in the Spanish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2010.08295.X

Familial hemolytic-uremic syndrome and homozygous factor H deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2010.08295.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2010.08295.X

Complement. First of two parts

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2141.2010.08295.X

10.1111/J.1365-2141.2010.08295.X

21 January 2018

Identifiers

DOI

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26 July 2017

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