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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
1999-12-16
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pubmed:abstractText |
Apolipoprotein E expression is increased in regenerating neural tissue and the APOE epsilon4 allele is associated with impaired neuronal repair. Since repair is essential for the restoration of central nervous system function following multiple sclerosis (MS) relapses, APOE genotype may influence clinical progression of the disease.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0003-9942
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1484-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10593303-Adult,
pubmed-meshheading:10593303-Alleles,
pubmed-meshheading:10593303-Apolipoprotein E4,
pubmed-meshheading:10593303-Apolipoproteins E,
pubmed-meshheading:10593303-Disability Evaluation,
pubmed-meshheading:10593303-Disease Progression,
pubmed-meshheading:10593303-Female,
pubmed-meshheading:10593303-Genetic Predisposition to Disease,
pubmed-meshheading:10593303-Genotype,
pubmed-meshheading:10593303-Humans,
pubmed-meshheading:10593303-Male,
pubmed-meshheading:10593303-Multiple Sclerosis, Relapsing-Remitting,
pubmed-meshheading:10593303-Pilot Projects,
pubmed-meshheading:10593303-Predictive Value of Tests,
pubmed-meshheading:10593303-Prognosis
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pubmed:year |
1999
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pubmed:articleTitle |
Preliminary observations on APOE epsilon4 allele and progression of disability in multiple sclerosis.
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pubmed:affiliation |
Department of Neurology and Neuroimmunology Clinic, Tel Aviv Medical Center, Israel.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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