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Browsing by Author Ruxrungtham, K.
Showing results 1 to 18 of 18
| Full Text | Issue Date | Title | Author(s) | | 2011 | Thai HIV-1-infected women do not require a dose increase of lopinavir/ritonavir during the third trimester of pregnancy. | Ramautarsing, R.A.; Lugt, J. van der; Gorowara, M.; Kerr, S.J.; Burger, D.M., et al |
| 2010 | Pharmacokinetics of low-dose protease inhibitors and efavirenz in low- and middle-income countries. | Gorowara, M.; Burger, D.M.; Hill, A.; Ruxrungtham, K. |
| 2009 | The pharmacokinetics, safety and efficacy of boosted saquinavir tablets in HIV type-1-infected pregnant women. | Lugt, J. van der; Colbers, A.; Molto, J.; Hawkins, D.; Ende, M. van der, et al |
| 2009 | A low dose of ritonavir-boosted atazanavir provides adequate pharmacokinetic parameters in HIV-1-infected Thai adults. | Avihingsanon, A.; Lugt, J. van der; Kerr, S.J.; Gorowara, M.; Chanmano, S., et al |
| 2009 | Reducing the boosting dose of ritonavir does not affect saquinavir plasma concentrations in HIV-1-infected individuals. | Lugt, J. van der; Gorowara, M.; Avihingsanon, A.; Burger, D.M.; Ananworanich, J., et al |
| 2009 | Pharmacokinetics and 48 week efficacy of low-dose lopinavir/ritonavir in HIV-infected children. | Puthanakit, T.; Lugt, J. van der; Bunupuradah, T.; Ananworanich, J.; Gorowara, M., et al |
| 2009 | Plasma concentrations of generic lopinavir/ritonavir in HIV type-1-infected individuals. | Lugt, J. van der; Lange, J.; Avihingsanon, A.; Ananworanich, J.; Sealoo, S., et al |
| 2009 | Safety and efficacy of a double-boosted protease inhibitor combination, saquinavir and lopinavir/ritonavir, in pretreated children at 96 weeks. | Bunupuradah, T.; Lugt, J. van der; Kosalaraksa, P.; Engchanil, C.; Boonrak, P., et al |
| 2008 | Double boosted protease inhibitors, saquinavir, and lopinavir/ritonavir, in nucleoside pretreated children at 48 weeks. | Kosalaraksa, P.; Bunupuradah, T.; Engchanil, C.; Boonrak, P.; Intasan, J., et al |
| 2008 | Pharmacokinetics and 48-week efficacy of nevirapine: 400 mg versus 600 mg per day in HIV-tuberculosis coinfection receiving rifampicin. | Avihingsanon, A.; Manosuthi, W.; Kantipong, P.; Chuchotaworn, C.; Moolphate, S., et al |
| 2008 | Pharmacokinetics and short-term efficacy of a double-boosted protease inhibitor regimen in treatment-naive HIV-1-infected adults. | Lugt, J. van der; Autar, R.S.; Ubolyam, S.; Garcia, E.F.; Sankote, J., et al |
| 2007 | Ketoconazole is inferior to ritonavir as an alternative booster for saquinavir in a once daily regimen in Thai HIV-1 infected patients. | Autar, R.S.; Wit, F.W.; Sankote, J.; Sutthichom, D.; Kimenai, E., et al |
| 2006 | The use of pharmacokinetically guided indinavir dose reductions in the management of indinavir-associated renal toxicity. | Boyd, M.A.; Siangphoe, U.; Ruxrungtham, K.; Reiss, P.; Mahanontharit, A., et al |
| 2006 | Boosted versus unboosted indinavir with zidovudine and lamivudine in nucleoside pre-treated patients: a randomized, open-label trial with 112 weeks of follow-up (HIV-NAT 005). | Boyd, M.A.; Srasuebkul, P.; Khongphattanayothin, M.; Ruxrungtham, K.; Hassink, E.A.M., et al |
| 2005 | Nevirapine plasma concentrations and concomitant use of rifampin in patients coinfected with HIV-1 and tuberculosis. | Autar, S.R.; Wit, F.W.; Sankote, J.; Mahanontharit, A.; Anekthananon, T., et al |
| 2005 | Pharmacokinetics and 24-week efficacy/safety of dual boosted saquinavir/lopinavir/ritonavir in nucleoside-pretreated children. | Ananworanich, J.; Kosalaraksa, P.; Hill, A.; Siangphoe, U.; Bergshoeff, A.S., et al |
| 2005 | Pharmacokinetics of reduced-dose indinavir/ritonavir 400/100 mg twice daily in HIV-1-infected Thai patients. | Boyd, M.; Mootsikapun, P.; Burger, D.M.; Chuenyam, T.; Ubolyam, S., et al |
| 2004 | Pharmacokinetic study of saquinavir hard gel caps/ritonavir in HIV-1-infected patients: 1600/100 mg once-daily compared with 2000/100 mg once-daily and 1000/100 mg twice-daily. | Autar, R.S.; Ananworanich, J.; Apateerapong, W.; Sankote, J.; Hill, A., et al |
Showing results 1 to 18 of 18
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