Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency (Q33385035)

26 July 2017

title

Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency (English)

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atypical hemolytic uremic syndrome

26 July 2017

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based on heuristic

inferred from title

author

Marie-Agnès Dragon-Durey

9

object named as

Marie-Agnès Dragon-Durey

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Soo Heon Kwak

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Soo Heon Kwak

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author name string

Beom Hee Lee

1

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26 July 2017

Jae Il Shin

3

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26 July 2017

So Hee Lee

4

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26 July 2017

Hyun Jin Choi

5

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26 July 2017

Hee Gyung Kang

6

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26 July 2017

Il Soo Ha

7

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26 July 2017

Jae Seung Lee

8

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26 July 2017

Yong Choi

10

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26 July 2017

Hae Il Cheong

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26 July 2017

language of work or name

English

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publication date

1 September 2009

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26 July 2017

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26 July 2017

volume

66

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26 July 2017

issue

3

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26 July 2017

page(s)

336-340

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Hemolytic Uremic Syndrome

26 July 2017

cites work

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https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Atypical haemolytic uraemic syndrome

21 January 2018

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Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

21 January 2018

1 reference

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Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Atypical haemolytic uraemic syndrome and mutations in complement regulator genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Complement factor H: sequence analysis of 221 kb of human genomic DNA containing the entire fH, fHR-1 and fHR-3 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

The factor H protein family

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Murine protein H is comprised of 20 repeating units, 61 amino acids in length

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Hemolytic uremic syndrome: an example of insufficient complement regulation on self-tissue

21 January 2018

1 reference

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Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Complement regulatory genes and hemolytic uremic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

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/10.1203%2FPDR.0B013E3181B1BD4A

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

Anti-Factor H autoantibodies in a fifth renal transplant recipient with atypical hemolytic and uremic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181B1BD4A

10.1203/PDR.0B013E3181B1BD4A

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

26 July 2017

1032718562

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