(Q33398546)

English

Factor H and CFHR1 polymorphisms associated with atypical Haemolytic Uraemic Syndrome (aHUS) are differently expressed in Tunisian and in Caucasian populations

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 July 2017

Factor H and CFHR1 polymorphisms associated with atypical Haemolytic Uraemic Syndrome (aHUS) are differently expressed in Tunisian and in Caucasian populations (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

author name string

N Leban

1

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26 July 2017

C Abarrategui-Garrido

2

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26 July 2017

E Fariza-Requejo

3

1 reference

Europe PubMed Central

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26 July 2017

C Amiñoso-Carbonero

4

1 reference

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26 July 2017

S Pinto

5

1 reference

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26 July 2017

J B Chibani

6

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26 July 2017

A H Khelil

7

1 reference

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26 July 2017

P Sánchez-Corral

8

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26 July 2017

publication date

5 December 2011

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26 July 2017

International Journal of Immunogenetics

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26 July 2017

39

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26 July 2017

2

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26 July 2017

110-113

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PubMed publication ID

26 July 2017

Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

A rapid method for the purification of DNA from blood

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Multiple gene polymorphisms in the complement factor h gene are associated with exudative age-related macular degeneration in chinese

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Atypical hemolytic-uremic syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1744-313X.2011.01071.X

21 January 2018

Identifiers

10.1111/J.1744-313X.2011.01071.X

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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