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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
22
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pubmed:dateCreated |
2003-11-17
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pubmed:abstractText |
The aim of this study was to evaluate (1) homocysteinemia and the prevalence of the C677T MTHFR polymorphism in Marfan patients and (2) whether the severity of cardiovascular manifestations is associated with homocysteinemia and/or C677T polymorphism.
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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:month |
Nov
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pubmed:issn |
0195-668X
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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 |
2038-45
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14613740-Adolescent,
pubmed-meshheading:14613740-Adult,
pubmed-meshheading:14613740-Aneurysm, Dissecting,
pubmed-meshheading:14613740-Aortic Aneurysm,
pubmed-meshheading:14613740-Cardiovascular Diseases,
pubmed-meshheading:14613740-Female,
pubmed-meshheading:14613740-Homocysteine,
pubmed-meshheading:14613740-Humans,
pubmed-meshheading:14613740-Hyperhomocysteinemia,
pubmed-meshheading:14613740-Logistic Models,
pubmed-meshheading:14613740-Male,
pubmed-meshheading:14613740-Marfan Syndrome,
pubmed-meshheading:14613740-Methylenetetrahydrofolate Reductase (NADPH2),
pubmed-meshheading:14613740-Middle Aged,
pubmed-meshheading:14613740-Phenotype,
pubmed-meshheading:14613740-Polymorphism, Genetic,
pubmed-meshheading:14613740-Severity of Illness Index
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pubmed:year |
2003
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pubmed:articleTitle |
Phenotypic variability of cardiovascular manifestations in Marfan Syndrome. Possible role of hyperhomocysteinemia and C677T MTHFR gene polymorphism.
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pubmed:affiliation |
Dipartimento di Area Critica Medico Chirurgica, University of Florence, Florence, Italy. labtrombosi@ao-careggi.toscana.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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