Source:http://linkedlifedata.com/resource/pubmed/id/12407291
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4 Pt 1
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pubmed:dateCreated |
2002-10-30
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pubmed:abstractText |
Pulmonary alveolar proteinosis is a progressive disease recognized 35 years ago. Many etiologies have been put forward, but the pathogenesis remains obscure. Familial alveolar proteinosis is a rare condition, probably transmitted by recessive autosomal inheritance, with deficiency in surfactant apoprotein SPB or defective expression of the common granulocyte colony stimulating factor (GM-CSF), IL3 and IL5 receptor. Gene therapy could be a future option for treatment in patients with specific gene defects.
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pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0761-8417
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
58
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
245-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12407291-Adult,
pubmed-meshheading:12407291-Bronchoalveolar Lavage,
pubmed-meshheading:12407291-Female,
pubmed-meshheading:12407291-Humans,
pubmed-meshheading:12407291-Immunoglobulin G,
pubmed-meshheading:12407291-Pulmonary Alveolar Proteinosis,
pubmed-meshheading:12407291-Remission, Spontaneous
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pubmed:year |
2002
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pubmed:articleTitle |
[Familial alveolar proteinosis].
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pubmed:affiliation |
Service de Pneumologie, CHU Hédi-Chaker, Sfax, Tunisie. Hajer@medscape.com
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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