pubmed-article:18476292 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C0679646 | lld:lifeskim |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C1442488 | lld:lifeskim |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C1963724 | lld:lifeskim |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:18476292 | lifeskim:mentions | umls-concept:C0205164 | lld:lifeskim |
pubmed-article:18476292 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:18476292 | pubmed:dateCreated | 2008-5-12 | lld:pubmed |
pubmed-article:18476292 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18476292 | pubmed:abstractText | The SMART study randomized 5,472 human immunodeficiency virus (HIV)-infected patients with CD4+ cell counts >350 cells/microL to intermittent antiretroviral therapy (ART; the drug conservation [DC] group) versus continuous ART (the viral suppression [VS] group). In the DC group, participants started ART when the CD4+ cell count was <250 cells/microL. Clinical outcomes in participants not receiving ART at entry inform the early use of ART. | lld:pubmed |
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pubmed-article:18476292 | pubmed:language | eng | lld:pubmed |
pubmed-article:18476292 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18476292 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:18476292 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18476292 | pubmed:month | Apr | lld:pubmed |
pubmed-article:18476292 | pubmed:issn | 0022-1899 | lld:pubmed |
pubmed-article:18476292 | pubmed:author | pubmed-author:PhillipsAndre... | lld:pubmed |
pubmed-article:18476292 | pubmed:author | pubmed-author:LawMatthewM | lld:pubmed |
pubmed-article:18476292 | pubmed:author | pubmed-author:GatellJose... | lld:pubmed |
pubmed-article:18476292 | pubmed:author | pubmed-author:EmerySeanS | lld:pubmed |
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pubmed-article:18476292 | pubmed:author | pubmed-author:Strategies... | lld:pubmed |
pubmed-article:18476292 | pubmed:author | pubmed-author:GrundBirgitB | lld:pubmed |
pubmed-article:18476292 | pubmed:author | pubmed-author:NeuhausJacque... | lld:pubmed |
pubmed-article:18476292 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18476292 | pubmed:day | 15 | lld:pubmed |
pubmed-article:18476292 | pubmed:volume | 197 | lld:pubmed |
pubmed-article:18476292 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18476292 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18476292 | pubmed:pagination | 1133-44 | lld:pubmed |
pubmed-article:18476292 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:18476292 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18476292 | pubmed:articleTitle | Major clinical outcomes in antiretroviral therapy (ART)-naive participants and in those not receiving ART at baseline in the SMART study. | lld:pubmed |
pubmed-article:18476292 | pubmed:affiliation | Therapeutic and Vaccine Research Program, National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, 376 Victoria St., Sydney, NSW 2010, Australia. semery@nchecr.unsw.edu.au | lld:pubmed |
pubmed-article:18476292 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18476292 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:18476292 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:18476292 | pubmed:publicationType | Multicenter Study | lld:pubmed |
pubmed-article:18476292 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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