pubmed-article:10348250 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0011315 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0042769 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0442886 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0014441 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0683441 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0680536 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0439831 | lld:lifeskim |
pubmed-article:10348250 | lifeskim:mentions | umls-concept:C0205225 | lld:lifeskim |
pubmed-article:10348250 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:10348250 | pubmed:dateCreated | 1999-6-8 | lld:pubmed |
pubmed-article:10348250 | pubmed:abstractText | A commercial capture ELISA for specific IgM and IgG antibodies produced during dengue infection (PanBio Dengue Duo) showed excellent sensitivity (99%, n = 78) using sera collected at hospital discharge compared with established ELISA and hemagglutination inhibition (HAI) assays. Furthermore, the ELISA was able to diagnose 79% of the dengue cases using sera collected at hospital admission. The ELISA also showed high specificity (92%) in paired sera from patients without flavivirus infection (n = 26), although 45% of the patients with Japanese encephalitis (n = 20) showed elevation of IgG but not IgM. The IgG capture ELISA showed good correlation with the HAI assay (r = 0.83, P < 0.0001), and IgG levels could be used to distinguish between primary and secondary infection, with 100% of primary infections and 96% of secondary infections being correctly classified. This ELISA should prove useful in the clinical diagnosis of dengue infections. | lld:pubmed |
pubmed-article:10348250 | pubmed:language | eng | lld:pubmed |
pubmed-article:10348250 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10348250 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:10348250 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10348250 | pubmed:month | Apr | lld:pubmed |
pubmed-article:10348250 | pubmed:issn | 0002-9637 | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:SolomonTT | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:DevineP LPL | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:NisalakAA | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:VaughnD WDW | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:KalayanaroojS... | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:NguyenM DMD | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:KneenRR | lld:pubmed |
pubmed-article:10348250 | pubmed:author | pubmed-author:CuzzubboAA | lld:pubmed |
pubmed-article:10348250 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10348250 | pubmed:volume | 60 | lld:pubmed |
pubmed-article:10348250 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10348250 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10348250 | pubmed:pagination | 693-8 | lld:pubmed |
pubmed-article:10348250 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:10348250 | pubmed:year | 1999 | lld:pubmed |
pubmed-article:10348250 | pubmed:articleTitle | Rapid serologic diagnosis of dengue virus infection using a commercial capture ELISA that distinguishes primary and secondary infections. | lld:pubmed |
pubmed-article:10348250 | pubmed:affiliation | United States Army Medical Component-Armed Forces Research Institute of Medical Science, Bangkok, Thailand. | lld:pubmed |
pubmed-article:10348250 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10348250 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
pubmed-article:10348250 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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