(Q50305793)

English

Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.

scientific article published in January 1992

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

Possible association of the extended MHC haplotype B44-SC30-DR4 with autism. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

0 references

author name string

R P Warren

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

V K Singh

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

P Cole

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

J D Odell

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

C B Pingree

5

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

W L Warren

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

C W DeWitt

7

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

M McCullough

8

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

language of work or name

0 references

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

36

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

203-207

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

https://scigraph.springernature.com/pub.10.1007/bf00215048

0 references

Autism and genetics. A decade of research

1 reference

https://api.crossref.org/works/10.1007%2FBF00215048

21 January 2018

Abnormal immune response to brain tissue antigen in the syndrome of autism

1 reference

https://api.crossref.org/works/10.1007%2FBF00215048

21 January 2018

Increased frequency of the null allele at the complement C4b locus in autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complotypes and extended haplotypes in laboratory medicine

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Depressed lymphocyte responsiveness in autistic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Demonstration of inter- and intraspecies differences in serotonin binding sites by antibodies from an autistic child

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autistic children exhibit undetectable hemagglutination-inhibition antibody titers despite previous rubella vaccination

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immune abnormalities in patients with autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Molecular Basis for MHC Class II—Associated Autoimmunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of suppressor-inducer (CD4+CD45RA+) T cells in autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement factor C4 in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up report on autism in congenital rubella

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autistic symptoms in a child with congenital cytomegaloviras infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic influences and infantile autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some disease-associated ancestral haplotypes carry a polymorphism of TNF.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CD4+ helper T cell depression in autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1639438

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00215048

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/1639438

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