Source:http://linkedlifedata.com/resource/pubmed/id/19188378
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2009-3-20
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pubmed:abstractText |
The fluconazole MIC distributions for Candida glabrata from testing 34 different clinical isolates and performing 51 tests on a single isolate mirrored each other. Since what is perceived as biological variation in isolates without resistance mechanisms is mainly methodological variation, breakpoints which divide this distribution not only lack a sound biological basis but also result in poor reproducibility of susceptibility characterization. This makes 2, 4, 8, and possibly 16 microg/ml unsuitable breakpoints for C. glabrata and fluconazole.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1098-6596
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1628-9
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading | |
pubmed:year |
2009
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pubmed:articleTitle |
Breakpoints for susceptibility testing should not divide wild-type distributions of important target species.
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pubmed:affiliation |
Unit of Mycology, Statens Serum Institut, Copenhagen, Denmark. mad@ssi.dk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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