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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1989-12-20
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pubmed:abstractText |
Familial Mediterranean fever is an autosomal recessively inherited disorder of unknown cause characterized by recurrent attacks of inflammation, involving mainly the peritoneum, pleura, synovia, and skin. Based on a phenotype analysis, we propose that its manifestations may be related to a genetic defect in one of the family of lipocortin proteins. Evidence is presented supporting an abnormality in the first step of prostaglandin/leukotriene synthesis.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0148-7299
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
163-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2530899-Annexins,
pubmed-meshheading:2530899-Calcium-Binding Proteins,
pubmed-meshheading:2530899-Diet,
pubmed-meshheading:2530899-Estrogens,
pubmed-meshheading:2530899-Familial Mediterranean Fever,
pubmed-meshheading:2530899-Genes, Recessive,
pubmed-meshheading:2530899-Humans,
pubmed-meshheading:2530899-Phospholipases
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pubmed:year |
1989
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pubmed:articleTitle |
Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?
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pubmed:affiliation |
Medical Genetics Birth Defects Center, Ahmanson Pediatric Center, Los Angeles, CA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Review,
Research Support, Non-U.S. Gov't
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