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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2007-7-2
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pubmed:abstractText |
We sought to determine both the procedural performance and safety of percutaneous implantation of the second (21-French [F])- and third (18-F)-generation CoreValve aortic valve prosthesis (CoreValve Inc., Irvine, California).
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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 |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1558-3597
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pubmed:author |
pubmed-author:BonanRaoulR,
pubmed-author:BuellesfeldLutzL,
pubmed-author:CartierRaymondR,
pubmed-author:FelderhoffThomasT,
pubmed-author:GerckensUlrichU,
pubmed-author:GrubeEberhardE,
pubmed-author:IversenSteinS,
pubmed-author:LinkeAxelA,
pubmed-author:MohrFriedrich-WilhelmFW,
pubmed-author:SaurenBarthelB,
pubmed-author:SchulerGerhardG,
pubmed-author:WaltherThomasT,
pubmed-author:WenaweserPeterP,
pubmed-author:ZickmannBernfriedB
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pubmed:issnType |
Electronic
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pubmed:day |
3
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
69-76
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pubmed:dateRevised |
2008-2-5
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pubmed:meshHeading |
pubmed-meshheading:17601548-Age Factors,
pubmed-meshheading:17601548-Aged,
pubmed-meshheading:17601548-Aged, 80 and over,
pubmed-meshheading:17601548-Aortic Valve Stenosis,
pubmed-meshheading:17601548-Bioprosthesis,
pubmed-meshheading:17601548-Female,
pubmed-meshheading:17601548-Follow-Up Studies,
pubmed-meshheading:17601548-Heart Catheterization,
pubmed-meshheading:17601548-Heart Valve Prosthesis Implantation,
pubmed-meshheading:17601548-Humans,
pubmed-meshheading:17601548-Male,
pubmed-meshheading:17601548-Prospective Studies,
pubmed-meshheading:17601548-Prosthesis Design,
pubmed-meshheading:17601548-Risk Assessment,
pubmed-meshheading:17601548-Severity of Illness Index,
pubmed-meshheading:17601548-Single-Blind Method,
pubmed-meshheading:17601548-Survival Rate,
pubmed-meshheading:17601548-Treatment Outcome
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pubmed:year |
2007
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pubmed:articleTitle |
Percutaneous aortic valve replacement for severe aortic stenosis in high-risk patients using the second- and current third-generation self-expanding CoreValve prosthesis: device success and 30-day clinical outcome.
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pubmed:affiliation |
HELIOS Heart Center Siegburg, Siegburg, Germany. GrubeE@aol.com
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Multicenter Study
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