(Q41737414)

8 October 2017

title

Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

author name string

J. M. Delâge

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

G. Lehner-Netsch

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

R. Lafleur

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

J. Simard

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

G. Brun

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

E. Prochazka

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

language of work or name

1 reference

1 June 1979

1 reference

full work available at URL

8 October 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/468307/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468307

4 July 2022

1 reference

8 October 2017

volume

37

1 reference

8 October 2017

issue

2

1 reference

8 October 2017

page(s)

419-428

1 reference

Genetic deficiency of the second component of complement (C2) associated with systemic lupus erythematosus. Relation of the complement abnormality and disease manifestations

8 October 2017

cites work

1 reference

12 December 2020

Complement testing in the diagnosis of immune and autoimmune diseases

1 reference

12 December 2020

Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian family

1 reference

12 December 2020

Inherited deficiency of the sixth component of complement: a silent or null gene

1 reference

12 December 2020

Genetics of the complement system

1 reference

12 December 2020

Toxoplasmosis dangerous in complement deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary C2 deficiency: Genetic studies and association with the HL-A system

1 reference

12 December 2020

Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement.

1 reference

12 December 2020

A blood coagulation abnormality in rabbits deficient in the sixth component of complement (C6) and its correction by purified C6

1 reference

12 December 2020

Protective function of C6 in rabbits treated with bacterial endotoxin

1 reference

12 December 2020

Methods for the separation, purification and measurement of nine components of hemolytic complement in guinea-pig serum

1 reference

12 December 2020

Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studies

1 reference

12 December 2020

Hereditary deficiency of the sixth component of complement in man. II. Studies of hemostasis

1 reference

12 December 2020

Identifiers

PMC publication ID

1457517

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=468307

4 July 2022

1 reference