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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1-2
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pubmed:dateCreated |
2003-12-3
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pubmed:abstractText |
Hyperhomocysteinemia is an independent risk factor for cerebrovascular disease and the homozygous C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene can induce hyperhomocysteinemia. However, the association between this 677TT genotype and ischemic stroke still remains controversial. Therefore, we carried out this study to determine whether the MTHFR TT genotype is associated with certain subtypes of ischemic stroke.
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pubmed:commentsCorrections |
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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 |
0049-3848
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
111
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
39-44
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14644077-Arterial Occlusive Diseases,
pubmed-meshheading:14644077-Arterioles,
pubmed-meshheading:14644077-Cytosine,
pubmed-meshheading:14644077-Female,
pubmed-meshheading:14644077-Genotype,
pubmed-meshheading:14644077-Homozygote,
pubmed-meshheading:14644077-Humans,
pubmed-meshheading:14644077-Male,
pubmed-meshheading:14644077-Methylenetetrahydrofolate Reductase (NADPH2),
pubmed-meshheading:14644077-Middle Aged,
pubmed-meshheading:14644077-Odds Ratio,
pubmed-meshheading:14644077-Polymorphism, Single Nucleotide,
pubmed-meshheading:14644077-Risk Factors,
pubmed-meshheading:14644077-Thymine
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pubmed:year |
2003
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pubmed:articleTitle |
Homozygous C677T mutation in the MTHFR gene as an independent risk factor for multiple small-artery occlusions.
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pubmed:affiliation |
Department of Neurology, College of Medicine, Pochon CHA University, Sungnam, South Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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