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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
|
pubmed:dateCreated |
1998-2-11
|
pubmed:abstractText |
Human interferon-gamma receptor 1 (IFNGR-1) deficiency is a newly identified autosomal recessive inherited immune disorder. Children with IFNGR-1 deficiency exhibit a severe, profound and selective susceptibility to weakly virulent mycobacteria, such as bacillus Calmette-Guerin (BCG) vaccine or environmental nontuberculous mycobacteria (NTM). This review compares the infections found in IFNGR-1-deficient children to those in IFN-gamma-deficient or IFNGR-1-deficient mice.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1079-9907
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
17
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
583-7
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:9355958-Animals,
pubmed-meshheading:9355958-Bacterial Infections,
pubmed-meshheading:9355958-Child,
pubmed-meshheading:9355958-Humans,
pubmed-meshheading:9355958-Infection,
pubmed-meshheading:9355958-Interferon-gamma,
pubmed-meshheading:9355958-Mice,
pubmed-meshheading:9355958-Parasitic Diseases,
pubmed-meshheading:9355958-Receptors, Interferon,
pubmed-meshheading:9355958-Virus Diseases
|
pubmed:year |
1997
|
pubmed:articleTitle |
Infections in IFNGR-1-deficient children.
|
pubmed:affiliation |
INSERM U429, Hôpital Necker-Enfants Malades, Paris, France.
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pubmed:publicationType |
Journal Article,
Review
|