Inherited complement component deficiencies in membranoproliferative glomerulonephritis (Q71172970)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

title

Inherited complement component deficiencies in membranoproliferative glomerulonephritis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

membranoproliferative glomerulonephritis

16 October 2019

main subject

1 reference

T H Coleman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

J Forristal

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

T Kosaka

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

C D West

series ordinal

4

1 reference

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16 October 2019

language of work or name

English

0 references

publication date

1 November 1983

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

volume

24

1 reference

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16 October 2019

issue

5

1 reference

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16 October 2019

page(s)

681-690

1 reference

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https://scigraph.springernature.com/pub.10.1038/ki.1983.211

16 October 2019

exact match

0 references

cites work

Familial C1q deficiency in 3 siblings with glomerulonephritis and Rothmund-Thomson syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Lupus-erythematosus-like syndrome with a familial defect of complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Inborn Clr deficiency with a mild lupus-like syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Genetics of complement deficiencies associated with lupus-like syndromes

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Deficiency of C7 with systemic lupus erythematosus: solubilization of immune complexes in complement-deficient sera

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Pathways of complement activation in glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Inherited deficiency of the second component of complement (C2) with membranoproliferative glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

The complement system in chronic glomerulonephritis: Three newly associated aberrations

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Inherited deficiency of the second component of complement. Rheumatic disease associations

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Partial H (beta 1H) deficiency and glomerulonephritis in two families

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

The chronic glomerulonephritides of childhood. Part II (2)

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Hypocomplementemic and normocomplementemic acute nephritis in children: a comparison with respect to etiology, clinical manifestations, and glomerular morphology

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Classical complement pathway activation in membranoproliferative glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Agarose isoelectric focusing of native human immunoglobulin M and α2-macroglobulin

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Genetic control of the eighth component of complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Linkage studies with C6

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Inherited structural variation and linkage relationships of C7

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Serum Complement Levels in Infancy: Age Related Changes

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Neisseria meningitidis and Neisseria gonorrhoeae Bacteremia Associated with C6, C7, or C8 Deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

A new complement function: solubilization of antigen-antibody aggregates

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Studies on the mechanism of solubilization of immune precipitates by serum

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Selective deficiency of the second component of complement in a patient with anaphylactoid purpura

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Biosynthetic Defect in Monocytes from Human Beings with Genetic Deficiency of the Second Component of Complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1983.211

7 January 2021

Identifiers

DOI

10.1038/KI.1983.211

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6663990%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference