Dense deposit disease and C3 glomerulopathy (Q37286653)

19 August 2017

6 references

7 March 2019

13 March 2019

9 October 2019

27 November 2019

13 December 2019

14 October 2020

Dense deposit disease and C3 glomerulopathy (English)

1 reference

membranoproliferative glomerulonephritis

19 August 2017

6 references

7 March 2019

13 March 2019

9 October 2019

27 November 2019

13 December 2019

14 October 2020

1 reference

9 October 2019

1 reference

27 November 2019

1 reference

13 December 2019

complement system proteins

1 reference

14 October 2020

Thomas D Barbour

1

0 references

Matthew C Pickering

object named as

Matthew C Pickering

series ordinal

2

0 references

author name string

H Terence Cook

series ordinal

3

1 reference

19 August 2017

1 November 2013

8 references

19 August 2017

7 March 2019

13 March 2019

9 October 2019

27 November 2019

13 December 2019

29 May 2020

14 October 2020

Seminars in Nephrology

7 references

19 August 2017

7 March 2019

13 March 2019

9 October 2019

27 November 2019

13 December 2019

14 October 2020

33

1 reference

19 August 2017

6

1 reference

19 August 2017

493-507

1 reference

Genotype/phenotype correlations in complement factor H deficiency arising from uniparental isodisomy

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

C3 glomerulonephritis associated with monoclonal gammopathy: a case series.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Dimerization of complement factor H-related proteins modulates complement activation in vivo

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Alternative pathway dysfunction in kidney disease: a case report and review of dense deposit disease and C3 glomerulopathy.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Tissue-specific host recognition by complement factor H is mediated by differential activities of its glycosaminoglycan-binding regions

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Combination of factor H mutation and properdin deficiency causes severe C3 glomerulonephritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Loss of properdin exacerbates C3 glomerulopathy resulting from factor H deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Dense deposit disease in Korean children: a multicenter clinicopathologic study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Thrombotic microangiopathy and associated renal disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

A hybrid CFHR3-1 gene causes familial C3 glomerulopathy.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Acute presentation and persistent glomerulonephritis following streptococcal infection in a patient with heterozygous complement factor H-related protein 5 deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Eculizumab and Refractory Membranoproliferative Glomerulonephritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Eculizumab for the Treatment of Dense-Deposit Disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Eculizumab in a patient with dense-deposit disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Eculizumab for dense deposit disease and C3 glomerulonephritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Causes of alternative pathway dysregulation in dense deposit disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Clinical features and outcomes of 98 children and adults with dense deposit disease.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Allelic variants of complement genes associated with dense deposit disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

6 September 2017

Dense deposit disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Genome-wide association study identifies susceptibility loci for IgA nephropathy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

The development of atypical hemolytic uremic syndrome depends on complement C5

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Recurrence of complement factor H-related protein 5 nephropathy in a renal transplant

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Dense Deposit Disease Associated With Monoclonal Gammopathy of Undetermined Significance

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

C3 glomerulopathy: a new classification

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Proliferative glomerulonephritis with monoclonal IgG deposits.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

New approaches to the treatment of dense deposit disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Dense deposit disease is not a membranoproliferative glomerulonephritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Familial membranoproliferative glomerulonephritis type III

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Hereditary complement factor I deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Mesangiocapillary glomerulonephritis: A long-term study of 40 cases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Hypocomplementæmic Membranoproliferative Glomerulonephritis and Nephrotic Syndrome Associated with Partial Lipodystrophy of the Face and Trunk

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Activation of the alternative pathway of complement by monoclonal lambda light chains in membranoproliferative glomerulonephritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Dense deposit disease: a variant of membranoproliferative glomerulonephritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Recurrent Glomerulonephritis After Renal Transplantation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Membranoproliferative glomerulonephritis (MPGN type I) and dense deposit disease (DDD) in children

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

The clinical course associated with dense deposits in the kidney basement membranes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Membranoproliferative glomerulonephritis with dense intramembranous alterations. A clinicopathologic study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Factor H facilitates the clearance of GBM bound iC3b by controlling C3 activation in fluid phase

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Pathology after eculizumab in dense deposit disease and C3 GN.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Inherited factor H deficiency and collagen type III glomerulopathy

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Recurrence of an original glomerular lesion in three renal allografts

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Glomerulonephritis with basement membrane dense deposits

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

The morphological and clinical features of membranoproliferative glomerulonephritis in adults.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

[Application of immunofluorescence to renal pathology. II. Immunohistochemical study of glomerular lesions]

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3).

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

[Intercapillary deposits of IgA-IgG]

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Serum C'3 lytic system in patients with glomerulonephritis

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Hypocomplementemic glomerulonephritis in an infant and mother. Evidence for an abnormal form of C3.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Fundus changes in (type II) mesangiocapillary glomerulonephritis simulating drusen: a histopathological report

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Familial incidence of C3 nephritic factor, partial lipodystrophy and membranoproliferative glomerulonephritis

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Treatment of mesangiocapillary glomerulonephritis with alternate-day prednisone--a report of the International Study of Kidney Disease in Children

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Membranoproliferative glomerulonephritis with disruption of the glomerular basement membrane

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Mesangiocapillary glomerulonephritis with dense "deposits" in the basement membranes of the kidney

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Idiopathic membranoproliferative (mesangiocapillary) glomerulonephritis: a clinicopathologic study

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Clinical and pathological features of dense deposit disease in Chinese patients.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Factor H autoantibodies in membranoproliferative glomerulonephritis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Membranoproliferative glomerulonephritis in a girl and her mother

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Severity of primary MPGN, rather than MPGN type, determines renal survival and post-transplantation recurrence risk

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Recurrence of membranoproliferative glomerulonephritis type II in renal allografts: The North American Pediatric Renal Transplant Cooperative Study experience

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Management of membranoproliferative glomerulonephritis type II with plasmapheresis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H

3 September 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

20 October 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

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

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3820036

Renal transplantation in patients with dense deposit disease: morphological characteristics of recurrent disease and clinical outcome

3 December 2018

1 reference

12 December 2020

Spontaneous clinical improvement in dense deposit disease

1 reference

12 December 2020

Electron dense alteration of kidney basement membranes. A renal lesion specific of a systemic disease

1 reference

12 December 2020

Acute non-proliferative glomerulitis: a cause of renal failure unique to children

1 reference

12 December 2020

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

1 reference

12 December 2020

Another example of spontaneous improvement in a case of dense deposit disease

1 reference

12 December 2020

Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: a long-term follow-up

1 reference

12 December 2020

C3 nephritic factor (C3NeF): stabilization of fluid phase and cell-bound alternative pathway convertase

1 reference

12 December 2020

The Complement Abnormalities of Lipodystrophy

1 reference

12 December 2020

Crescentic glomerulonephritis in childhood: acute nonproliferative glomerulitis versus dense deposit disease

1 reference

12 December 2020

[Unusual change of the basal membranes of the kidney.]

1 reference

12 December 2020

DENSE DEPOSITS WITHIN THE BASAL MEMBRANES OF THE KIDNEY. OPTICAL AND ELECTRON MICROSCOPIC STUDY

1 reference

12 December 2020

Prognosis, treatment and outcome of childhood mesangiocapillary (membranoproliferative) glomerulonephritis

1 reference

12 December 2020

C3 deposition glomerulopathy due to a functional factor H defect

1 reference

12 December 2020

Familial incidence of C3 nephritic factor

1 reference

12 December 2020

Anti-factor B autoantibody in dense deposit disease

1 reference

12 December 2020

Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation

1 reference

12 December 2020

Heterogeneous pattern of renal disease associated with homozygous Factor H deficiency

1 reference

12 December 2020

Two types of C3 nephritic factor: properdin-dependent C3NeF and properdin-independent C3NeF

1 reference

12 December 2020

Combined C3b and factor B autoantibodies and MPGN type II

1 reference

12 December 2020

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

1 reference

12 December 2020

C3 glomerulopathy masquerading as acute postinfectious glomerulonephritis

1 reference

12 December 2020

The many faces of C3 glomerulopathy

1 reference

12 December 2020

Dense intramembranous deposit disease: a clinical comparison of histological subtypes

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial membranoproliferative glomerulonephritis type 2 (MPGN-2)

1 reference

12 December 2020

A rare case: childhood-onset C3 glomerulonephritis due to homozygous factor H deficiency

1 reference

12 December 2020

A properdin dependent nephritic factor slowly activating C3, C5, and C9 in membranoproliferative glomerulonephritis, types I and III

1 reference

12 December 2020

H deficiency in two brothers with atypical dense intramembranous deposit disease

1 reference

12 December 2020

Regression of Membranoproliferative Glomerulonephritis Type II (Dense Deposit Disease): Observations in Six Children

1 reference

12 December 2020

Effect of nephritic factor on C3 and on the terminal pathway of complement in vivo and in vitro

1 reference

12 December 2020

Idiopathic membranoproliferative glomerulonephritis. Morphology and natural history

1 reference

12 December 2020

Renal disease in partial lipodystrophy

1 reference

12 December 2020

[Parietoproliferative glomerulonephritis--(P.P.G.N.). Histopathological study under optic and electron microscopy and with immunochemistry of 49 cases. Anatomo-clinical correlations]

1 reference

12 December 2020

2 cases of membrano-proliferative glomerulonephritis associated with partial lipodistrophy of facio-truncal type

1 reference

12 December 2020

Incidence and prognostic importance of glomerular crescents in renal diseases of childhood

1 reference

12 December 2020

An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis

1 reference

12 December 2020

Characteristics of a benign subtype of dense deposit disease: comparison with the progressive form of this disease

1 reference

12 December 2020

Membranoproliferative glomerulonephritis in two sibships

1 reference

12 December 2020

Paramesangial glomerular deposits in membranoproliferative glomerulonephritis type II correlate with hypocomplementemia

1 reference

12 December 2020

Non-nephrotic children with membranoproliferative glomerulonephritis: are steroids indicated?

1 reference

12 December 2020

Outcome of idiopathic membranoproliferative glomerulonephritis in children. Arbeitsgemeinschaft Pädiatrische Nephrologie

1 reference

12 December 2020

Dense deposit disease in association with monoclonal gammopathy of unknown significance

1 reference

12 December 2020

The prognostic value of some clinical and histological parameters in membranoproliferative glomerulonephritis (MPGN): report of 112 cases

1 reference

12 December 2020

In situ complement activation in porcine membranoproliferative glomerulonephritis type II

1 reference

12 December 2020

10.1016/J.SEMNEPHROL.2013.08.002

Identifiers

DOI

1 reference

19 August 2017

1 reference

PMC publication ID

3820036

19 August 2017

PubMed publication ID

24161036

1 reference

PMC publication ID

3820036