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https://ir.swu.ac.th/jspui/handle/123456789/14896
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Manosuthi W. | |
dc.contributor.author | Sungkanuparph S. | |
dc.contributor.author | Ruxrungtham K. | |
dc.contributor.author | Prasithsirikul W. | |
dc.contributor.author | Athichathanabadi C. | |
dc.contributor.author | Tantisiriwat W. | |
dc.contributor.author | Bowonwatanuwong C. | |
dc.contributor.author | Chumpathat N. | |
dc.contributor.author | Chaovavanich A. | |
dc.date.accessioned | 2021-04-05T04:32:04Z | - |
dc.date.available | 2021-04-05T04:32:04Z | - |
dc.date.issued | 2008 | |
dc.identifier.issn | 15254135 | |
dc.identifier.other | 2-s2.0-39049117418 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14896 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-39049117418&doi=10.1097%2fQAI.0b013e318157b0da&partnerID=40&md5=9c6cb1be2c5626aefcfeb310a21297cf | |
dc.description.abstract | [No abstract available] | |
dc.subject | atazanavir | |
dc.subject | proteinase inhibitor | |
dc.subject | ritonavir | |
dc.subject | RNA directed DNA polymerase inhibitor | |
dc.subject | saquinavir | |
dc.subject | virus RNA | |
dc.subject | atazanavir | |
dc.subject | oligopeptide | |
dc.subject | proteinase inhibitor | |
dc.subject | pyridine derivative | |
dc.subject | ritonavir | |
dc.subject | saquinavir | |
dc.subject | adult | |
dc.subject | aminotransferase blood level | |
dc.subject | blood sampling | |
dc.subject | CD4 lymphocyte count | |
dc.subject | clinical article | |
dc.subject | controlled study | |
dc.subject | DNA polymorphism | |
dc.subject | drug blood level | |
dc.subject | drug efficacy | |
dc.subject | drug safety | |
dc.subject | drug tolerability | |
dc.subject | dyslipidemia | |
dc.subject | female | |
dc.subject | high performance liquid chromatography | |
dc.subject | human | |
dc.subject | Human immunodeficiency virus infection | |
dc.subject | hyperbilirubinemia | |
dc.subject | letter | |
dc.subject | low drug dose | |
dc.subject | male | |
dc.subject | practice guideline | |
dc.subject | priority journal | |
dc.subject | salvage therapy | |
dc.subject | side effect | |
dc.subject | steady state | |
dc.subject | treatment duration | |
dc.subject | treatment outcome | |
dc.subject | virus resistance | |
dc.subject | article | |
dc.subject | drug administration | |
dc.subject | drug combination | |
dc.subject | Drug Administration Schedule | |
dc.subject | Drug Therapy, Combination | |
dc.subject | HIV Infections | |
dc.subject | HIV Protease Inhibitors | |
dc.subject | Humans | |
dc.subject | Oligopeptides | |
dc.subject | Pyridines | |
dc.subject | Ritonavir | |
dc.subject | Saquinavir | |
dc.title | Plasma levels, safety, and 60-week efficacy of a once-daily double-boosted protease inhibitor regimen of atazanavir, saquinavir, and ritonavir | |
dc.type | Letter | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Journal of Acquired Immune Deficiency Syndromes. Vol 47, No.1 (2008), p.127-129 | |
dc.identifier.doi | 10.1097/QAI.0b013e318157b0da | |
Appears in Collections: | Scopus 1983-2021 |
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