Familial C1q deficiency associated with renal and cutaneous disease (Q71562438)

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scientific article published on 01 April 1981

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Language	Label	Description	Also known as
English	Familial C1q deficiency associated with renal and cutaneous disease	scientific article published on 01 April 1981

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

title

Familial C1q deficiency associated with renal and cutaneous disease (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

author name string

Leyva-Cobián F

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

Moneo I

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

Mampaso F

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

Sánchez-Bayle M

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

Ecija JL

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

Bootello A

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

publication date

1 April 1981

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

published in

Clinical and Experimental Immunology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

volume

44

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

page(s)

173-180

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

cites work

Familial deficiency of two subunits of the first component of complement. C1r and C1s associated with a lupus erythematosus-like disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationships between the haemolytic activities of the human complement system and complement components

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C1q: isolation from human serum in high yield by affinity chromatography and development of a highly sensitive hemolytic assay

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inborn Clr deficiency with a mild lupus-like syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and immunological studies in a case of selective complete C1q deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic defect of the C1q subcomponent of complement associated with childhood (immune complex) nephritis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Precise Standardization of Reagents for Complement Fixation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased C'-1q protein concentration and agglutinating activity in agammaglobulinaemia syndromes: an inborn error reflected in the complement system

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual complement deficiency in a patient with disseminated lupus erythematosus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Precipitin reactions of the C1q component of complement with aggregated gamma-globulin and immune complexes in gel diffusion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C1r, subunit of the first complement component: purification, properties, and assay based on its linking role

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolism of human C1q. Studies in hypogammaglobulinemia, myeloma, and systemic lupus erythematosus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro adherence of soluble immune complexes to macrophages

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reconstitution of Clq after bone marrow transplantation in patients with severe combined immunodeficiency.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypocomplementemia with cutaneous vasculitis and arthritis: a new syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persistent Clq deficiency in a patient with a systemic lupus erythematosus-like syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The autosomal recessive mode of inheritance of C1r deficiency in a large Puerto Rican family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blood levels of the proactivator of the C 3 fraction of complement in glomerular nephropathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysis of RNA tumor viruses by human serum: direct antibody-independent triggering of the classical complement pathway

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The nature of immune complexes in human cancer sera

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type c viruses and systemic lupus erythematosus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low molecular weight C1q-precipitins in hypocomplementemic vasculitis-urticaria syndrome: partial purification and characterization as immunoglobulin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement genetics in relation to HLA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6790209

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PubMed publication ID

6790209

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6790209

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6790209%20AND%20SRC:MED&resulttype=core&format=json

retrieved

19 October 2019

 

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