| pubmed-article:12149389 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C2347026 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C0370003 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C0597198 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C0032520 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C1826383 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C0883241 | lld:lifeskim |
| pubmed-article:12149389 | lifeskim:mentions | umls-concept:C1510438 | lld:lifeskim |
| pubmed-article:12149389 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:12149389 | pubmed:dateCreated | 2002-7-31 | lld:pubmed |
| pubmed-article:12149389 | pubmed:abstractText | We compared the performance of two PCR assays, an IS6110-based in-house protocol and the COBAS AMPLICOR MTB PCR (COBAS MTB) system, for the detection of Mycobacterium tuberculosis complex in 43 human lymph node samples from 40 patients. For the in-house PCR and the COBAS MTB assays, respectively, sensitivities were 87.5% versus 45.5% (P < 0.05), specificities were 100.0% versus 91.3% (P > 0.05), and inhibition rates were 4.8% versus 19.5% (P < 0.05). For the COBAS MTB system, additional N-acetyl-L-cysteine-NaOH pretreatment of the samples changed neither the inhibition rate nor the sensitivity significantly. | lld:pubmed |
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| pubmed-article:12149389 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12149389 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12149389 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:12149389 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12149389 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:12149389 | pubmed:issn | 0095-1137 | lld:pubmed |
| pubmed-article:12149389 | pubmed:author | pubmed-author:RimekDagmarD | lld:pubmed |
| pubmed-article:12149389 | pubmed:author | pubmed-author:TyagiSachinS | lld:pubmed |
| pubmed-article:12149389 | pubmed:author | pubmed-author:KappeReinhard... | lld:pubmed |
| pubmed-article:12149389 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12149389 | pubmed:volume | 40 | lld:pubmed |
| pubmed-article:12149389 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12149389 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12149389 | pubmed:pagination | 3089-92 | lld:pubmed |
| pubmed-article:12149389 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:12149389 | pubmed:meshHeading | pubmed-meshheading:12149389... | lld:pubmed |
| pubmed-article:12149389 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12149389 | pubmed:articleTitle | Performance of an IS6110-based PCR assay and the COBAS AMPLICOR MTB PCR system for detection of Mycobacterium tuberculosis complex DNA in human lymph node samples. | lld:pubmed |
| pubmed-article:12149389 | pubmed:affiliation | Department of Medical Microbiology and Hospital Hygiene, University Hospital, D-18057 Rostock, Germany. dagmar.rimek@med.uni-rostock.de | lld:pubmed |
| pubmed-article:12149389 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12149389 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:12149389 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:12149389 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
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