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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2006-12-21
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pubmed:abstractText |
To assess whether polymorphism of the macrophage migration inhibitory factor (MIF) gene at position -173 was implicated in the incidence of Henoch-Schönlein purpura (HSP) and cutaneous leukocytoclastic angiitis (CLA). A further objective was to determine if any relationship existed with severe systemic complications of HSP, in particular with severe renal involvement and permanent renal dysfunction.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0392-856X
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
576-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17181929-Adolescent,
pubmed-meshheading:17181929-Adult,
pubmed-meshheading:17181929-Aged,
pubmed-meshheading:17181929-Child,
pubmed-meshheading:17181929-Child, Preschool,
pubmed-meshheading:17181929-Female,
pubmed-meshheading:17181929-Gene Frequency,
pubmed-meshheading:17181929-Genetic Predisposition to Disease,
pubmed-meshheading:17181929-Genotype,
pubmed-meshheading:17181929-Humans,
pubmed-meshheading:17181929-Kidney,
pubmed-meshheading:17181929-Kidney Diseases,
pubmed-meshheading:17181929-Macrophage Migration-Inhibitory Factors,
pubmed-meshheading:17181929-Male,
pubmed-meshheading:17181929-Middle Aged,
pubmed-meshheading:17181929-Polymorphism, Genetic,
pubmed-meshheading:17181929-Purpura, Schoenlein-Henoch,
pubmed-meshheading:17181929-Vasculitis, Leukocytoclastic, Cutaneous
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pubmed:articleTitle |
Lack of association between macrophage migration inhibitory factor gene (-173 G/C) polymorphism and cutaneous vasculitis.
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pubmed:affiliation |
The Endocrinology and Metabolism Research Centre, Tehran University of Medical Sciences, Tehran, Iran.
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pubmed:publicationType |
Journal Article
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