(Q39869252)

15 September 2017

title

Hypomorphic variant of C3, arthritis, and chronic glomerulonephritis (English)

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

16 December 2022

1 reference

R. H. McLean

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A152808

16 December 2022

A. Weinstein

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A152808

16 December 2022

I. Damjanov

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A152808

16 December 2022

N. Rothfield

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A152808

16 December 2022

language of work or name

English

0 references

publication date

1 December 1978

1 reference

full work available at URL

15 September 2017

https://api.elsevier.com/content/article/PII:S0022347678812153?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

https://api.elsevier.com/content/article/PII:S0022347678812153?httpAccept=text/plain

16 December 2022

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

The Journal of Pediatrics

16 December 2022

published in

1 reference

15 September 2017

volume

93

1 reference

15 September 2017

issue

6

1 reference

15 September 2017

page(s)

937-943

1 reference

Genetic polymorphism of the third component of human complement (C'3).

15 September 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

High-voltage starch-gel electrophoresis in the study of post-albumin proteins and C'3 (�1e-globulin) polymorphism

16 December 2022

2

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Allotypes of complement components in man

16 December 2022

3

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Studies of the C3 polymorphism. Relationship between phenotype and conversion rate in vitro

16 December 2022

5

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

The HLA system and inherited deficiencies of the complement system

16 December 2022

6

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Studies of a hypomorphic variant of human C3

16 December 2022

7

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Recurrence of membranoproliferative glomerulonephritis following kidney transplantation. Serum complement component studies

16 December 2022

8

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

High voltage agarose gel electrophoresis in the study of C 3 polymorphism

16 December 2022

9

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Inherited deficiency of the third component of human complement (C′3)

16 December 2022

11

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Homozygous deficiency of C3 in a patient with repeated infections

16 December 2022

12

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Complete absence of the third component of complement in man

16 December 2022

13

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Hereditary deficiency of the third component of complement in a child with fever, skin rash, and arthralgias: Response to transfusion of whole blood

16 December 2022

14

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

A family with partial and total deficiency of complement C3

16 December 2022

15

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

The complement system in chronic glomerulonephritis: Three newly associated aberrations

16 December 2022

16

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

C1r deficiency: an inborn error associated with cutaneous and renal disease

16 December 2022

17

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Linkage between the Gene (or Genes) Controlling Synthesis of the Fourth Component of Complement and the Major Histocompatibility Complex

16 December 2022

18

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

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

16 December 2022

19

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Immunity deficiency in pathogenesis of glomerulonephritis.

16 December 2022

20

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

Dense deposit disease: a variant of membranoproliferative glomerulonephritis

16 December 2022

21

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81215-3

16 December 2022

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=152808

16 December 2022

1 reference