(Q70775616)

English

Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura

scientific article published on 01 December 1984

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scholarly article

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13 October 2019

Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (English)

1 reference

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13 October 2019

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author name string

R H McLean

1

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13 October 2019

R J Wyatt

2

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13 October 2019

B A Julian

3

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1 December 1984

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13 October 2019

Kidney International

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13 October 2019

26

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13 October 2019

855-860

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13 October 2019

6

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13 October 2019

https://scigraph.springernature.com/pub.10.1038/ki.1984.228

0 references

Structural polymorphism of the fourth component of human complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

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inferred from DOI database lookup

Two HLA-linked loci controlling the fourth component of human complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited structural polymorphism of the fourth component of human complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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Genetic polymorphism of human complement C4 and detection of heterozygotes

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

Statement on the nomenclature of human C4 allotypes.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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BF types and the mode of inheritance of insulin-dependent diabetes mellitus (IDDM)

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

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Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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Human C4 polymorphism: pedigree analysis of qualitative, quantitative, and functional parameters as a basis for phenotype interpretations

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

IGA nephropathy in HLA-identical siblings

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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HLA-Bw35 and Mesangial IgA Glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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Higher Prevalence of HLA-B12 in Patients with IgA Nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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Family study in IgA nephritis: the possible role of HLA antigens

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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HLA antigen in three types of glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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The complement system in chronic glomerulonephritis: Three newly associated aberrations

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited complement component deficiencies in membranoproliferative glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic deficiency of C4 presenting with recurrent infections and a SLE-like disease. Genetic and immunologic studies

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

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Severe systemic lupus erythematosus with nephritis in a boy with deficiency of the fourth component of complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1984.228

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/KI.1984.228

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6533396%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6533396%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

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