Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case (Q33401621)

26 July 2017

title

Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case (English)

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atypical hemolytic uremic syndrome

26 July 2017

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Augusto Vaglio

3

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author name string

Elisa Gnappi

1

1 reference

26 July 2017

Marco Allinovi

2

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26 July 2017

Elena Bresin

4

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26 July 2017

Annalisa Sorosina

5

1 reference

26 July 2017

Francesco P Pilato

6

1 reference

26 July 2017

Landino Allegri

7

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26 July 2017

Lucio Manenti

8

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26 July 2017

publication date

5 June 2012

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26 July 2017

number of pages

5

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inferred from page(s)

published in

Pediatric Nephrology

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26 July 2017

volume

27

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26 July 2017

issue

10

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26 July 2017

page(s)

1995-1999

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Atypical hemolytic-uremic syndrome

26 July 2017

cites work

1 reference

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

21 January 2018

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Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

21 January 2018

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Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

21 January 2018

1 reference

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Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

21 January 2018

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An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations

21 January 2018

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DEAP-HUS: deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome

21 January 2018

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Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15.

21 January 2018

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

21 January 2018

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

21 January 2018

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Membranoproliferative glomerulonephritis--a new look at an old entity

21 January 2018

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Autoimmune forms of thrombotic microangiopathy and membranoproliferative glomerulonephritis: Indications for a disease spectrum and common pathogenic principles

21 January 2018

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

21 January 2018

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Three kidneys, two diseases, one antibody?

21 January 2018

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Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits

21 January 2018

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A clinicopathologic study of thrombotic microangiopathy in IgA nephropathy

21 January 2018

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Actual and future strategies for transplantation in atypical HUS associated with mutations in factor H.

21 January 2018

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aHUS caused by complement dysregulation: new therapies on the horizon

21 January 2018

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Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation

21 January 2018

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https://pubmed.ncbi.nlm.nih.gov/22669321

12 December 2020

inferred from PubMed ID database lookup

The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22669321

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inferred from PubMed ID database lookup

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

1 reference

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12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00467-012-2210-0

1 reference

Dimensions Publication ID

26 July 2017

1040397077

0 references

1 reference