Inherited deficiencies of complement proteins in man (Q40118356)

17 September 2017

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title

Inherited deficiencies of complement proteins in man (English)

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4 September 2023

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4 September 2023

author name string

C. A. Alper

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6238435

4 September 2023

F. S. Rosen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6238435

4 September 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6238435

4 September 2023

publication date

1 January 1984

1 reference

full work available at URL

17 September 2017

https://link.springer.com/content/pdf/10.1007/BF01893022.pdf

file format

Portable Document Format

1 reference

https://link.springer.com/article/10.1007/BF01893022/fulltext.html

4 September 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF01893022

4 September 2023

1 reference

Seminars in Immunopathology

4 September 2023

published in

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17 September 2017

volume

7

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17 September 2017

issue

2-3

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17 September 2017

page(s)

251-261

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

17 September 2017

cites work

1 reference

Crossref

Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies

21 January 2018

1 reference

12 December 2020

Hereditary deficiency of the second component of complement (C'2) in man.

1 reference

12 December 2020

Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysis

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Two types of dysfunctional eighth component of complement (C8) molecules in C8 deficiency in man. Reconstitution of normal C8 from the mixture of two abnormal C8 molecules

1 reference

12 December 2020

Hereditary angioedema and “familial” lupus erythematosus in identical twin boys

1 reference

12 December 2020

Recurrent septicemia associated with congenital deficiency of C2 and partial deficiency of factor B and the alternative complement pathway

1 reference

12 December 2020

Absence of the eighth component of complement in association with systemic lupus erythematosus-like disease

1 reference

12 December 2020

Properdin deficiency in a family with fulminant meningococcal infections.

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

C8 deficiency in a family with xeroderma pigmentosum. Lack of linkage to the HLA region

1 reference

12 December 2020

Genetic control of the eighth component of complement

1 reference

12 December 2020

Occurrence of an incomplete C8 molecule in homozygous C8 deficiency in man

1 reference

12 December 2020

Essential hypocomplementemia: report of a case

1 reference

12 December 2020

Homozygous deficiency of C3 in a patient with repeated infections

1 reference

12 December 2020

Acute lupus erythematosus with total absence of the C4 fraction of complement

1 reference

12 December 2020

Homozygous C3 deficiency: Detection of C3 by radioimmunoassay

1 reference

12 December 2020

Deficiency of the eighth component of complement and recurrent meningococcal disease: a case and family study

1 reference

12 December 2020

Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.

1 reference

12 December 2020

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

1 reference

12 December 2020

Complement-mediated solubilization in patients with systemic lupus erythematosus, nephritis or vasculitis

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

Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus

1 reference

12 December 2020

Genetic polymorphism in C8 beta-chains. Evidence for two unlinked genetic loci for the eighth component of human complement (C8)

1 reference

12 December 2020

Complement deficiency states

1 reference

12 December 2020

Increased Susceptibility to Infection in a Patient with Type II Essential Hypercatabolism of C3

1 reference

12 December 2020

Homozygous deficiency of the second component of complement presenting with recurrent bacterial meningitis

1 reference

12 December 2020

Mixed lymphocyte culture determinants and C2 deficiency: LD-7a associated with C2 deficiency in four families

1 reference

12 December 2020

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

1 reference

12 December 2020

A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE.

1 reference

12 December 2020

Human deficiency of the eighth component of complement. The requirement of C8 for serum Neisseria gonorrhoeae bactericidal activity

1 reference

12 December 2020

Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

1 reference

12 December 2020

Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3).

1 reference

12 December 2020

Hereditary deficiency of the second component of complement (C'2) in man: further observations on a second kindred

1 reference

12 December 2020

Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema

1 reference

12 December 2020

Genetic analysis of C4 deficiency

1 reference

12 December 2020

The complement system in chronic glomerulonephritis: Three newly associated aberrations

1 reference

12 December 2020

A new complement function: solubilization of antigen-antibody aggregates

1 reference

12 December 2020

Journal of Immunology

2

108

837

V Agnello

1972

1 reference

4 September 2023

16

27

589A

RHK Eng

1979

1 reference

Japanese Journal of Human Genetics

4 September 2023

25

26

163

T Kisu

1980

1 reference

4 September 2023

Journal of Immunology

27

98

72

MR Klemperer

1967

1 reference

4 September 2023

Journal of Immunology

32

4

425

HD Moore

1919

1 reference

4 September 2023

Identifiers

DOI

10.1007/BF01893022

1 reference

17 September 2017

1 reference