A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome. (Q33392449)

PubMed publication ID

20974643

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20974643%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

author name string

Tara K Maga

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

Nicole C Meyer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

Craig Belsha

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

Carla J Nishimura

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

Yuzhou Zhang

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

language of work or name

English

0 references

publication date

25 October 2010

1 reference

PubMed publication ID

20974643

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20974643%20AND%20SRC:MED&resulttype=core&format=json

Nephrology Dialysis Transplantation

14 January 2020

published in

1 reference

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13 May 2020

volume

26

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13 May 2020

issue

2

1 reference

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13 May 2020

page(s)

739-741

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

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

13 May 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Atypical hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Functional analysis in serum from atypical Hemolytic Uremic Syndrome patients reveals impaired protection of host cells associated with mutations in factor H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Hemolytic uremic syndrome recurrence after renal transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

Eculizumab for Atypical Hemolytic–Uremic Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFQ658

21 January 2018

Identifiers

DOI

10.1093/NDT/GFQ658

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6937010&resulttype=core&format=json

13 May 2020

PubMed publication ID

20974643

1 reference