Pathogenesis of the C3 glomerulopathies and reclassification of MPGN. (Q38048606)

27 August 2017

Pathogenesis of the C3 glomerulopathies and reclassification of MPGN. (English)

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27 August 2017

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Andrew S Bomback

1

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PubMed ID

23026947

27 August 2017

Gerald B Appel

series ordinal

2

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PubMed ID

23026947

27 August 2017

language of work or name

English

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publication date

2 October 2012

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Nature Reviews Nephrology

27 August 2017

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27 August 2017

8

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27 August 2017

634-642

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27 August 2017

11

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https://scigraph.springernature.com/pub.10.1038/nrneph.2012.213

27 August 2017

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Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

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

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

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Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation

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7 January 2021

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The role of complement and its receptor in the elimination of immune complexes

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Complement factor H deficiency accelerates development of lupus nephritis

21 January 2018

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Glomerulonephritis with isolated C3 deposits and monoclonal gammopathy: a fortuitous association?

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Dense deposit disease associated with monoclonal gammopathy of undetermined significance

21 January 2018

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Nephritic factor of the classical pathway of complement: immunoglobulin G autoantibody directed against the classical pathway C3 convetase enzyme

21 January 2018

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

21 January 2018

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

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The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria

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New treatment options for atypical hemolytic uremic syndrome with the complement inhibitor eculizumab

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Eculizumab for the Treatment of Dense-Deposit Disease

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Eculizumab in a patient with dense-deposit disease

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Recurrent glomerular diseases after renal transplantation.

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Complement inhibitor eculizumab in atypical hemolytic uremic syndrome

21 January 2018

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Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome

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Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

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Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis

31 March 2020

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C3 deposition glomerulopathy due to a functional factor H defect

31 March 2020

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

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The Complement Abnormalities of Lipodystrophy

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Combined C3b and factor B autoantibodies and MPGN type II

31 March 2020

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Mouse podocyte complement factor H: the functional analog to human complement receptor 1

31 March 2020

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C3 glomerulopathy masquerading as acute postinfectious glomerulonephritis

31 March 2020

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Recurrent dense deposit disease after renal transplantation: an emerging role for complementary therapies

31 March 2020

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Recurrent membranoproliferative glomerulonephritis after kidney transplantation

31 March 2020

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Recurrent type I membranoproliferative glomerulonephritis in a renal allograft: successful treatment with plasmapheresis

31 March 2020

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Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis

31 March 2020

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12 December 2020

Hypocomplementaemia of poststreptococcal acute glomerulonephritis is associated with C3 nephritic factor (C3NeF) IgG autoantibody activity

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12 December 2020

C3 nephritic factor and hypocomplementaemia in a clinically healthy individual

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12 December 2020

Membranoproliferative glomerulonephritis with disruption of the glomerular basement membrane

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12 December 2020

Identifiers

DOI

10.1038/NRNEPH.2012.213

1 reference

27 August 2017

1 reference

PubMed ID

23026947