Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees (Q35030648)

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31 January 2020

title

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

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author

Konstantinos Voskarides

2

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Daniel P Gale

3

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Constantinos Deltas

14

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7

Patrick H Maxwell

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12

Ioanna Zouvani

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31 January 2020

1

Yiannis Athanasiou

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13

Alkis Pierides

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11

Kyriacos Kyriacou

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8

H Terence Cook

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10

Andreas Hadjisavvas

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6

Michalis Zavros

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5

Charalambos Patsias

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author name string

Loukas Damianou

4

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Panayiota Demosthenous

9

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publication date

12 May 2011

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Clinical Journal of the American Society of Nephrology

31 January 2020

published in

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volume

6

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page(s)

1436-1446

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issue

6

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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

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C3 glomerulopathy: a new classification

8 July 2018

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

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

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Rat mesangial cells exhibit sex-specific profibrotic and proinflammatory phenotypes

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

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8 July 2018

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

8 July 2018

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Dense deposit disease is not a membranoproliferative glomerulonephritis

8 July 2018

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

8 July 2018

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

8 July 2018

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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

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

8 July 2018

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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

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

8 July 2018

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

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Acute interstitial nephritis superimposed on glomerulonephritis: report of a case

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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

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25 October 2018

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

25 October 2018

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12 December 2020

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

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12 December 2020

Clinicopathological features in patients with isolated C3 mesangial proliferative glomerulonephritis

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12 December 2020

Long-term evolution of patients with isolated C3 mesangial glomerulonephritis

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Identifiers

DOI

10.2215/CJN.09541010

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

31 January 2020

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31 January 2020

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