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1
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33846059449
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Causes of severe morbidity in HIV-infected patients. Aquitaine cohort 2000-2004: The importance of bacterial infections, cardio-vascular, digestive, and psychiatric morbidity
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Toronto, MOPDB02
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Bonnet F, et al: Causes of severe morbidity in HIV-infected patients. Aquitaine cohort 2000-2004: the importance of bacterial infections, cardio-vascular, digestive, and psychiatric morbidity, XVI International AIDS Conference, Toronto 2006, MOPDB02.
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(2006)
XVI International AIDS Conference
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Bonnet, F.1
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2
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33749850044
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Myocardial infarction rates among HIV-infected patients in a U.S. health care system
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Toronto, WEPE0179
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Triant V, et al: Myocardial infarction rates among HIV-infected patients in a U.S. health care system, XVI International AIDS Conference, Toronto 2006, WEPE0179.
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(2006)
XVI International AIDS Conference
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Triant, V.1
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3
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33749858914
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On behalf of the SPREAD-programme - Transmission of HIV drug resistance in Europe
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Toronto, TUAB0101
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Wensing AM: On behalf of the SPREAD-programme - Transmission of HIV drug resistance in Europe, XVI International AIDS Conference, Toronto 2006, TUAB0101.
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(2006)
XVI International AIDS Conference
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Wensing, A.M.1
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4
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33749843637
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Inferior clinical outcomes with episodic CD4-guided antiretroviral therapy aimed at drug conservation (DC) in SMART study: Consistency of finding in all patient subgroups
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for the SMART Study Group: Toronto, WEAB0204
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El-Sadr W; for the SMART Study Group: Inferior clinical outcomes with episodic CD4-guided antiretroviral therapy aimed at drug conservation (DC) in SMART study: consistency of finding in all patient subgroups, XVI International AIDS Conference, Toronto 2006, WEAB0204.
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(2006)
XVI International AIDS Conference
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El-Sadr, W.1
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5
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33749817739
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Immunological, virological and clinical changes during periods of transient viremia
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Toronto, TUPE0003
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van Sighem A, et al: Immunological, virological and clinical changes during periods of transient viremia, XVI International AIDS Conference, Toronto 2006, TUPE0003.
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(2006)
XVI International AIDS Conference
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Van Sighem, A.1
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6
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33749869583
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A prospective, randomized, phase III trial of NRTI-, PI-, and NNRTI-sparing regimens for initial treatment of HIV-1 infection-ACTG 5142
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for the AIDS Clinical Trials Group 5142 Study Team: Toronto, THLB0204
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Riddler SA; for the AIDS Clinical Trials Group 5142 Study Team: A prospective, randomized, phase III trial of NRTI-, PI-, and NNRTI-sparing regimens for initial treatment of HIV-1 infection-ACTG 5142, XVI International AIDS Conference, Toronto 2006, THLB0204.
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(2006)
XVI International AIDS Conference
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Riddler, S.A.1
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7
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33749867216
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The KLEAN Study: Fosamprenavir + ritonavir (FPV/r) versus lopinavir/ritonavir (LPV/r) in antiretroviral-naïve (ARTNaïve) HIV-1 infected adults over 48 weeks
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Toronto, THLB0205
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Eron J, et al: The KLEAN Study: fosamprenavir + ritonavir (FPV/r) versus lopinavir/ritonavir (LPV/r) in antiretroviral-naïve (ARTNaïve) HIV-1 infected adults over 48 weeks, XVI International AIDS Conference, Toronto 2006, THLB0205.
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(2006)
XVI International AIDS Conference
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Eron, J.1
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8
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33749842084
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Lopinavir/ritonavir as single-drug maintenance therapy in patients with HIV-1 viral suppression: Forty eight week results of a randomized, controlled, open label, clinical trial (OK04 Study)
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Toronto, THLB0203
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Arribas J, et al: Lopinavir/ritonavir as single-drug maintenance therapy in patients with HIV-1 viral suppression: forty eight week results of a randomized, controlled, open label, clinical trial (OK04 Study), XVI International AIDS Conference, Toronto 2006, THLB0203.
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(2006)
XVI International AIDS Conference
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Arribas, J.1
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9
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33749833424
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MONARK Trial (MONotherapy AntiRetroviral Kaletra): 48-Week analysis of lopinavir/ritonavir (LPV/r) monotherapy compared to LPV/r + zidovudine/ lamivudine (AZT/3TC) in antiretroviral-naïve patients
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Toronto, THLB0202
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Delfraissy JF, et al: MONARK Trial (MONotherapy AntiRetroviral Kaletra): 48-week analysis of lopinavir/ritonavir (LPV/r) monotherapy compared to LPV/r + zidovudine/lamivudine (AZT/3TC) in antiretroviral-naïve patients, XVI International AIDS Conference, Toronto 2006, THLB0202.
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(2006)
XVI International AIDS Conference
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Delfraissy, J.F.1
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10
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33749864294
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48-Week efficacy and safety results of simplification to single agent lopinavir/ritonavir (LPV/r) regimen in patients suppressed below 80 copies/ml on HAART - The KalMo study
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Toronto, TUAB0103
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Nunes EP, et al: 48-week efficacy and safety results of simplification to single agent lopinavir/ritonavir (LPV/r) regimen in patients suppressed below 80 copies/ml on HAART - the KalMo study, XVI International AIDS Conference, Toronto 2006, TUAB0103.
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(2006)
XVI International AIDS Conference
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Nunes, E.P.1
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11
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33749851581
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A two-year randomized controlled clinical trial in antiretroviral- naïve subjects using lopinavir/ritonavir (LPV/r) monotherapy after initial induction treatment compared to an efavirenz (EFV) 3-drug regimen (Study M03-613)
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Toronto, THLB0201
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Cameron W, et al: A two-year randomized controlled clinical trial in antiretroviral-naïve subjects using lopinavir/ritonavir (LPV/r) monotherapy after initial induction treatment compared to an efavirenz (EFV) 3-drug regimen (Study M03-613), XVI International AIDS Conference, Toronto 2006, THLB0201.
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(2006)
XVI International AIDS Conference
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Cameron, W.1
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12
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33749825229
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Efficacy and safety of tenofovir DF (TDF), emtricitabine (FTC) and efavirenz (EFV) compared to fixed dose zidovudine/lamivudine (CBV) and EFV through 96 weeks in antiretroviral treatment-naïve patients
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Toronto, TUPE0064
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Gallant J, et al: Efficacy and safety of tenofovir DF (TDF), emtricitabine (FTC) and efavirenz (EFV) compared to fixed dose zidovudine/lamivudine (CBV) and EFV through 96 weeks in antiretroviral treatment-naïve patients, XVI International AIDS Conference, Toronto 2006, TUPE0064.
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(2006)
XVI International AIDS Conference
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Gallant, J.1
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13
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84892252145
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TMC114/r in treatment-experienced HIV patients in power 3: 24-Week efficacy and safety analysis
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Toronto, TUPE0060
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Molina JM, et al: TMC114/r in treatment-experienced HIV patients in power 3: 24-week efficacy and safety analysis, XVI International AIDS Conference, Toronto 2006, TUPE0060.
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(2006)
XVI International AIDS Conference
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Molina, J.M.1
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14
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33845968601
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Efficacy and safety results at 48 weeks with the novel NNRTI, TMC125, and impact of baseline resistance on the virologic response in study TMC125-C223
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Toronto, TUPE0061
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Cohen C, et al: Efficacy and safety results at 48 weeks with the novel NNRTI, TMC125, and impact of baseline resistance on the virologic response in study TMC125-C223, XVI International AIDS Conference, Toronto 2006, TUPE0061.
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(2006)
XVI International AIDS Conference
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Cohen, C.1
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15
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33749839996
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Safety and efficacy of Maraviroc (MVC), a novel CCR5 antagonist, when used in combination with optimized background therapy (OBT) for the treatment of antiretroviral-experienced subjects infected with dual/mixed-tropic HIV-1: 24-Week results of a phase 2b exploratory trial
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Toronto, THLB0215
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Mayer H, et al: Safety and efficacy of Maraviroc (MVC), a novel CCR5 antagonist, when used in combination with optimized background therapy (OBT) for the treatment of antiretroviral-experienced subjects infected with dual/mixed-tropic HIV-1: 24-week results of a phase 2b exploratory trial, XVI International AIDS Conference, Toronto 2006, THLB0215.
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(2006)
XVI International AIDS Conference
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Mayer, H.1
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16
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33749865167
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Potent antiretroviral effect of MK-0518, a novel HIV-1 integrase inhibitor, as part of combination ART in treatment-naïve HIV-1 infected patients
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Toronto, THLB0214
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Markowitz M, et al: Potent antiretroviral effect of MK-0518, a novel HIV-1 integrase inhibitor, as part of combination ART in treatment-naïve HIV-1 infected patients, XVI International AIDS Conference, Toronto 2006, THLB0214.
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(2006)
XVI International AIDS Conference
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Markowitz, M.1
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17
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28444460441
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Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: The ANRS 1265 Trial
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Erratum in: PLoS Med 2006; 3(5): e298
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Auvert B, et al: Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 Trial. PLoS Med 2005; 2(11): e298. Erratum in: PLoS Med 2006; 3(5): e298.
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PLoS Med
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Auvert, B.1
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