(Q40646792)

22 September 2017

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title

Nephritic factors predispose to chronic glomerulonephritis (English)

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22 September 2017

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West CD

1

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22 September 2017

publication date

1 December 1994

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American Journal of Kidney Diseases

22 September 2017

published in

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22 September 2017

volume

24

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22 September 2017

issue

6

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22 September 2017

page(s)

956-963

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Dense deposit disease: a variant of membranoproliferative glomerulonephritis

22 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

Differences between membranoproliferative glomerulonephritis types I and III in clinical presentation, glomerular morphology, and complement perturbation

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

The alternative pathway of complement

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https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

Control of the amplification convertase of complement by the plasma protein beta1H

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https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

Patterns of complement activation in idiopathic membranoproliferative glomerulonephritis, types I, II, and III

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7 January 2021

Serum terminal complement component levels in hypocomplementemic glomerulonephritides.

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7 January 2021

The Complement Abnormalities of Lipodystrophy

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7 January 2021

Metabolism of the fifth component of complement, and its relation to metabolism of the third component, in patients with complement activation

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

H deficiency in two brothers with atypical dense intramembranous deposit disease

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7 January 2021

Hereditary, complete deficiency of complement factor H associated with recurrent meningococcal disease

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7 January 2021

Porcine membranoproliferative glomerulonephritis with intramembranous dense deposits (porcine dense deposit disease)

1 reference

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7 January 2021

Circulating immune complexes and glomerulonephritis in a patient with congenital absence of the third component of complement

1 reference

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7 January 2021

Membranoproliferative glomerulonephritis in a patient with congenital deficiency of the third component of complement: effect of treatment with plasma

1 reference

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7 January 2021

Serum beta-1C globulin levels in persistent glomerulonephritis with low serum complement: variability unrelated to clinical course

1 reference

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7 January 2021

Childhood membranoproliferative glomerulonephritis: an approach to management

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7 January 2021

Increased Susceptibility to Infection in a Patient with Type II Essential Hypercatabolism of C3

1 reference

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7 January 2021

Recurrent bacterial infections associated with C3 nephritic factor and hypocomplementemia

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7 January 2021

Recurrence of dense deposits in transplanted kidney: II. Serum complement and nephritic factor profiles

1 reference

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7 January 2021

Transplantation in mesangiocapillary glomerulonephritis with intramembranous dense "deposits": recurrence of disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

Genetics and deficiencies of the soluble regulatory proteins of the complement system

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2812%2981068-7

7 January 2021

10.1016/S0272-6386(12)81068-7

Identifiers

DOI

1 reference

22 September 2017

1 reference