C3 deposition glomerulopathy due to a functional factor H defect (Q81654240)

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10 January 2020

title

C3 deposition glomerulopathy due to a functional factor H defect (English)

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3

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9

Peter F Zipfel

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6

Christine Skerka

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7

Michael Kirschfink

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8

Bernd Hoppe

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10

Christoph Licht

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1

Sandra Habbig

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5

Mathias Emmel

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10 January 2020

author name string

Michael J Mihatsch

series ordinal

2

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Bodo Beck

series ordinal

4

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language of work or name

English

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publication date

16 July 2008

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10 January 2020

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10 January 2020

volume

75

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issue

11

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page(s)

1230-1234

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

10 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

Complement and diseases: defective alternative pathway control results in kidney and eye diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

MPGN II--genetically determined by defective complement regulation?

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

Cell biology of the glomerular podocyte

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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)

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

Secondary membranoproliferative glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.354

7 January 2021