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pubmed-article:16322490 | lifeskim:mentions | umls-concept:C0333516 | lld:lifeskim |
pubmed-article:16322490 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:16322490 | lifeskim:mentions | umls-concept:C0205217 | lld:lifeskim |
pubmed-article:16322490 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
pubmed-article:16322490 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
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pubmed-article:16322490 | lifeskim:mentions | umls-concept:C0205296 | lld:lifeskim |
pubmed-article:16322490 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:16322490 | pubmed:dateCreated | 2005-12-23 | lld:pubmed |
pubmed-article:16322490 | pubmed:abstractText | Identification of single-nucleotide polymorphisms (SNPs) associated with increased risk of new intracranial hemorrhage (ICH) after brain arteriovenous malformation (BAVM) diagnosis would facilitate risk stratification and identify potential targets for therapeutic intervention. | lld:pubmed |
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pubmed-article:16322490 | pubmed:language | eng | lld:pubmed |
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pubmed-article:16322490 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:16322490 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16322490 | pubmed:month | Jan | lld:pubmed |
pubmed-article:16322490 | pubmed:issn | 1524-4628 | lld:pubmed |
pubmed-article:16322490 | pubmed:author | pubmed-author:YoungWilliam... | lld:pubmed |
pubmed-article:16322490 | pubmed:author | pubmed-author:LawtonMichael... | lld:pubmed |
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pubmed-article:16322490 | pubmed:author | pubmed-author:AchrolAchal... | lld:pubmed |
pubmed-article:16322490 | pubmed:author | pubmed-author:UCSF BAVM... | lld:pubmed |
pubmed-article:16322490 | pubmed:author | pubmed-author:LeeChanhungC | lld:pubmed |
pubmed-article:16322490 | pubmed:author | pubmed-author:PoonK Y... | lld:pubmed |
pubmed-article:16322490 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:16322490 | pubmed:volume | 37 | lld:pubmed |
pubmed-article:16322490 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16322490 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16322490 | pubmed:pagination | 231-4 | lld:pubmed |
pubmed-article:16322490 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:16322490 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16322490 | pubmed:articleTitle | Tumor necrosis factor-alpha-238G>A promoter polymorphism is associated with increased risk of new hemorrhage in the natural course of patients with brain arteriovenous malformations. | lld:pubmed |
pubmed-article:16322490 | pubmed:affiliation | Department of Anesthesia and Perioperative Care, Center for Cerebrovascular Research, University of California, San Francisco, California, USA. | lld:pubmed |
pubmed-article:16322490 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16322490 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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