A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl (Q44309387)

1 December 2017

A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl (English)

1 reference

1 December 2017

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C3 glomerulonephritis

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Nesrin Besbas

1

1 reference

1 December 2017

Bora Gulhan

2

1 reference

1 December 2017

Safak Gucer

3

1 reference

1 December 2017

Emine Korkmaz

4

1 reference

1 December 2017

Fatih Ozaltin

5

1 reference

1 December 2017

5 December 2013

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1 December 2017

Journal of Nephrology

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1 December 2017

27

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1 December 2017

4

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1 December 2017

457-460

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https://scigraph.springernature.com/pub.10.1007/s40620-013-0008-1

1 December 2017

0 references

cites work

C3 glomerulopathy: a new classification

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Membranoproliferative glomerulonephritis--a new look at an old entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40620-013-0008-1

Recent insights into C3 glomerulopathy

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24536001

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Novel roles of complement in renal diseases and their therapeutic consequences

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24536001

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S40620-013-0008-1

1 reference

1 December 2017

1 reference