G Moyle

Summary

Country: UK

Publications

  1. ncbi Use of HIV protease inhibitors as pharmacoenhancers
    G Moyle
    Chelsea and Westminster Hospital, London
    AIDS Read 11:87-98; quiz 107-8. 2001
  2. ncbi The Assessing Patients' Preferred Treatments (APPT-1) study
    G Moyle
    HIV Research Department, Chelsea and Westminster Hospital, London, UK
    Int J STD AIDS 14:34-6. 2003
  3. ncbi The emerging roles of non-nucleoside reverse transcriptase inhibitors in antiretroviral therapy
    G Moyle
    HIV Research, Chelsea and Westminster Hospital, London, England
    Drugs 61:19-26. 2001
  4. ncbi Changes in sleep quality and brain wave patterns following initiation of an efavirenz-containing triple antiretroviral regimen
    G Moyle
    Chelsea and Westminster Hospital, London, UK
    HIV Med 7:243-7. 2006
  5. ncbi Pharmacokinetics and safety of saquinavir/ritonavir and omeprazole in HIV-infected subjects
    K Singh
    St Stephen s Centre, Chelsea and Westminster NHS Foundation Trust, London, UK
    Clin Pharmacol Ther 83:867-72. 2008
  6. ncbi Loss of the CD56hiCD16- NK cell subset and NK cell interferon-gamma production during antiretroviral therapy for HIV-1: partial recovery by human growth hormone
    M R Goodier
    Department of Immunology, Imperial College London, Faculty of Medicine, Chelsea and Westminster Hospital, London, UK
    Clin Exp Immunol 134:470-6. 2003
  7. ncbi Antiretroviral therapy for HIV-2 infected patients
    N A Smith
    Chelsea Hospital, London, UK
    J Infect 42:126-33. 2001
  8. ncbi Once-daily therapy: less is more
    G Moyle
    HIV Research Department, Chelsea and Westminster Hospital, London, UK
    Int J STD AIDS 14:1-5. 2003
  9. ncbi Resistance and cross-resistance to abacavir
    G Moyle
    HIV Research, Chelsea and Westminster Hospital, London, UK
    HIV Med 2:154-62. 2001
  10. ncbi Beliefs about antiretroviral therapy, treatment adherence and quality of life in a 48-week randomised study of continuation of zidovudine/lamivudine or switch to tenofovir DF/emtricitabine, each with efavirenz
    Vanessa Cooper
    Department of Practice and Policy, Centre for Behavioural Medicine, The School of Pharmacy, University of London, London, UK
    AIDS Care 23:705-13. 2011

Detail Information

Publications17

  1. ncbi Use of HIV protease inhibitors as pharmacoenhancers
    G Moyle
    Chelsea and Westminster Hospital, London
    AIDS Read 11:87-98; quiz 107-8. 2001
    ....
  2. ncbi The Assessing Patients' Preferred Treatments (APPT-1) study
    G Moyle
    HIV Research Department, Chelsea and Westminster Hospital, London, UK
    Int J STD AIDS 14:34-6. 2003
    ..504 people with HIV participated. Participants showed a preference for once-daily therapy administration. However, several factors affected this preference...
  3. ncbi The emerging roles of non-nucleoside reverse transcriptase inhibitors in antiretroviral therapy
    G Moyle
    HIV Research, Chelsea and Westminster Hospital, London, England
    Drugs 61:19-26. 2001
    ..The majority of adverse events with NNRTIs occur within the first month, and are predictable and manageable without therapy interruption...
  4. ncbi Changes in sleep quality and brain wave patterns following initiation of an efavirenz-containing triple antiretroviral regimen
    G Moyle
    Chelsea and Westminster Hospital, London, UK
    HIV Med 7:243-7. 2006
    ..Assessment of sleep using the electroencephalogram and electromyogram enables sleep staging to be performed and changes following the introduction of therapy to be evaluated...
  5. ncbi Pharmacokinetics and safety of saquinavir/ritonavir and omeprazole in HIV-infected subjects
    K Singh
    St Stephen s Centre, Chelsea and Westminster NHS Foundation Trust, London, UK
    Clin Pharmacol Ther 83:867-72. 2008
    ..No grade 3/4 toxicity or lab abnormalities were observed. In the presence of omeprazole, saquinavir plasma exposure is significantly increased in HIV-infected subjects whether administered simultaneously or 2 h apart...
  6. ncbi Loss of the CD56hiCD16- NK cell subset and NK cell interferon-gamma production during antiretroviral therapy for HIV-1: partial recovery by human growth hormone
    M R Goodier
    Department of Immunology, Imperial College London, Faculty of Medicine, Chelsea and Westminster Hospital, London, UK
    Clin Exp Immunol 134:470-6. 2003
    ..Furthermore, in these individuals HAART with growth hormone resulted in an enhancement of cytokine-driven NK cell activation and IFN-gamma production compared to the HAART-only baseline...
  7. ncbi Antiretroviral therapy for HIV-2 infected patients
    N A Smith
    Chelsea Hospital, London, UK
    J Infect 42:126-33. 2001
    ..The timing of therapy initiation, monitoring of response and the measurement of resistance remain unresolved issues and conclusions cannot be extrapolated from HIV-1...
  8. ncbi Once-daily therapy: less is more
    G Moyle
    HIV Research Department, Chelsea and Westminster Hospital, London, UK
    Int J STD AIDS 14:1-5. 2003
    ..The range of once-daily options is expanding rapidly, with the potential for two lines of once-daily therapy to be available in the next 12-18 months...
  9. ncbi Resistance and cross-resistance to abacavir
    G Moyle
    HIV Research, Chelsea and Westminster Hospital, London, UK
    HIV Med 2:154-62. 2001
    ..It may be used as a substitution agent for persons wishing to discontinue protease inhibitor therapy who have not previously experienced viral rebound on NRTI therapy...
  10. ncbi Beliefs about antiretroviral therapy, treatment adherence and quality of life in a 48-week randomised study of continuation of zidovudine/lamivudine or switch to tenofovir DF/emtricitabine, each with efavirenz
    Vanessa Cooper
    Department of Practice and Policy, Centre for Behavioural Medicine, The School of Pharmacy, University of London, London, UK
    AIDS Care 23:705-13. 2011
    ..Switching from CBV to TVD may improve patient reported outcomes including slightly better adherence, a greater reduction in concerns about adverse effects and less treatment intrusiveness...
  11. ncbi Toxicity of antiretroviral nucleoside and nucleotide analogues: is mitochondrial toxicity the only mechanism?
    G Moyle
    Chelsea and Westminster Hospital, London, England
    Drug Saf 23:467-81. 2000
    ..New research evaluating the effects of long term exposure of cell lines is required to address the possibility that nuclear genotoxicity plays a role in long term nucleoside analogue toxicity...
  12. ncbi Matched case-control study to evaluate risk factors for hyperlactataemia in HIV patients on antiretroviral therapy
    D Datta
    Kobler Clinic, Chelsea and Westminster Hospital, London, UK
    HIV Med 4:311-4. 2003
    ..The aim of this matched case-control study was to identify risk factors for hyperlactataemia requiring screening...
  13. ncbi Clinical manifestations and management of antiretroviral nucleoside analog-related mitochondrial toxicity
    G Moyle
    Chelsea and Westminster Hospital, London, United Kingdom
    Clin Ther 22:911-36; discussion 898. 2000
    ..This article reviews the clinical manifestations of mitochondrial toxicity associated with the use of nucleoside analog reverse transcriptase inhibitors (NRTIs) and outlines strategies to manage these sequelae...
  14. ncbi British HIV Association (BHIVA) guidelines for the treatment of HIV-infected adults with antiretroviral therapy
    A Pozniak
    Chelsea and Westminster Hospital, London, UK
    HIV Med 4:1-41. 2003
  15. ncbi Restoration of human immunodeficiency virus-1-specific responses in patients changing from protease to non-nucleoside reverse transcriptase inhibitor-based antiretroviral therapy
    A K Sullivan
    Department of Immunology, ICSTM, Chelsea and Westminster Hospital, London, UK
    Scand J Immunol 57:600-7. 2003
    ....
  16. ncbi Relative antiviral efficacy of ritonavir-boosted darunavir and ritonavir-boosted tipranavir vs. control protease inhibitor in the POWER and RESIST trials
    A Hill
    Department of Pharmacology, University of Liverpool, Liverpool, UK
    HIV Med 8:259-64. 2007
    ....
  17. ncbi Once-daily atazanavir/ritonavir versus twice-daily lopinavir/ritonavir, each in combination with tenofovir and emtricitabine, for management of antiretroviral-naive HIV-1-infected patients: 48 week efficacy and safety results of the CASTLE study
    Jean Michel Molina
    Department of Infectious Diseases, Saint Louis Hospital, AP HP, Paris University of Paris Diderot, Paris 7, France
    Lancet 372:646-55. 2008
    ..We compared these two combinations directly in treatment-naive patients...