(Q37770399)

22 August 2017

1 reference

title

C3 glomerulopathy: a new classification (English)

1 reference

Véronique Frémeaux-Bacchi

22 August 2017

author

2

object named as

Véronique Frémeaux-Bacchi

1 reference

22 August 2017

Matthew C Pickering

5

0 references

author name string

Fadi Fakhouri

1

1 reference

22 August 2017

Laure-Hélène Noël

3

1 reference

22 August 2017

H Terence Cook

4

1 reference

22 August 2017

language of work or name

English

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publication date

6 July 2010

1 reference

Nature Reviews Nephrology

22 August 2017

published in

1 reference

22 August 2017

volume

6

1 reference

22 August 2017

issue

8

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22 August 2017

page(s)

494-499

1 reference

https://scigraph.springernature.com/pub.10.1038/nrneph.2010.85

22 August 2017

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Dense deposit disease: a variant of membranoproliferative glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Dense deposit disease is not a membranoproliferative glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (Type I MPGN)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Functional basis of protection against age-related macular degeneration conferred by a common polymorphism in complement factor B

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Where next with atypical hemolytic uremic syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Complement regulatory genes and hemolytic uremic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Complement and the atypical hemolytic uremic syndrome in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

New approaches to the treatment of dense deposit disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Glomeruli of Dense Deposit Disease contain components of the alternative and terminal complement pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Continuing C3 breakdown after bilateral nephrectomy in patients with membrano-proliferative glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Membranoproliferative glomerulonephritis type II (dense deposit disease): an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Idiopathic mesangiocapillary glomerulonephritis. Comparison of types I and II in children and adults and long-term prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Familial membranoproliferative glomerulonephritis type III

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Therapeutic potential of complement modulation

21 January 2018

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The amplification loop of the complement pathways.

21 January 2018

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Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis

31 March 2020

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Composition of nephritic factor-generated glomerular deposits in membranoproliferative glomerulonephritis type 2

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Mesangiocapillary glomerulonephritis type II (dense-deposit disease): clinical features of progressive disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

A mutant complement factor H-related 5 protein is associated with familial C3 glomerulonephritis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Anti-C1q autoantibodies deposit in glomeruli but are only pathogenic in combination with glomerular C1q-containing immune complexes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Systemic lupus erythematosus, complement deficiency, and apoptosis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.85

Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20606628

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Membranoproliferative glomerulonephritis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20606628

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Factor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20606628

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRNEPH.2010.85

1 reference

22 August 2017

1 reference