(Q35030648)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21566112%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21566112%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

author

Konstantinos Voskarides

2

1 reference

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31 January 2020

Daniel P Gale

3

1 reference

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31 January 2020

Constantinos Deltas

14

1 reference

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31 January 2020

7

Patrick H Maxwell

1 reference

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31 January 2020

12

Ioanna Zouvani

1 reference

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31 January 2020

1

Yiannis Athanasiou

1 reference

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31 January 2020

13

Alkis Pierides

1 reference

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31 January 2020

11

Kyriacos Kyriacou

1 reference

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31 January 2020

8

H Terence Cook

1 reference

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31 January 2020

10

Andreas Hadjisavvas

1 reference

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31 January 2020

6

Michalis Zavros

1 reference

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31 January 2020

5

Charalambos Patsias

1 reference

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31 January 2020

author name string

Loukas Damianou

4

1 reference

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31 January 2020

Panayiota Demosthenous

9

1 reference

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31 January 2020

publication date

12 May 2011

1 reference

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Clinical Journal of the American Society of Nephrology

31 January 2020

published in

1 reference

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31 January 2020

volume

6

1 reference

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31 January 2020

page(s)

1436-1446

1 reference

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31 January 2020

issue

6

1 reference

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

31 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

C3 glomerulopathy: a new classification

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Treatment with human complement factor H rapidly reverses renal complement deposition in factor H-deficient mice

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Familial IgA nephropathy in southeastern Kentucky

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

The complement fitness factor H: role in human diseases and for immune escape of pathogens, like pneumococci

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Rat mesangial cells exhibit sex-specific profibrotic and proinflammatory phenotypes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Incidence of thin basement membrane nephropathy in 990 consecutive renal biopsies examined with electron microscopy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Dense deposit disease is not a membranoproliferative glomerulonephritis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

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)

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Human factor H-related protein 5 (FHR-5). A new complement-associated protein

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Age and gender-related incidence of chronic renal failure in a French urban area: a prospective epidemiologic study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Acute interstitial nephritis superimposed on glomerulonephritis: report of a case

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidn

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

COL4A3 founder mutations in Greek-Cypriot families with thin basement membrane nephropathy and focal segmental glomerulosclerosis dating from around 18th century.

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Clinicopathologic features, outcome, and therapeutic interventions in four children with isolated C3 mesangial proliferative glomerulonephritis

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: impact on clinical counselling

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109942

C3 deposition glomerulopathy due to a functional factor H defect

25 October 2018

1 reference

12 December 2020

COL4A3/COL4A4Mutations Link Familial Hematuria and Focal Segmental Glomerulosclerosis. Glomerular Epithelium Destruction via Basement Membrane Thinning?

1 reference

12 December 2020

Clinicopathological features in patients with isolated C3 mesangial proliferative glomerulonephritis

1 reference

12 December 2020

Long-term evolution of patients with isolated C3 mesangial glomerulonephritis

1 reference

12 December 2020

A new etiology of episcleritis: nephropathies with IgA and/or isolated C3 deposits

1 reference

12 December 2020

Sixteen novel mutations identified in COL4A3, COL4A4, and COL4A5 genes in Slovenian families with Alport syndrome and benign familial hematuria

1 reference

12 December 2020

Identifiers

DOI

10.2215/CJN.09541010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21566112%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21566112%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference