“High” antiretroviral deintensification, a strategy to avoid drug interactions and unfavourable long-term effects of HAART-Reference-Cited by-同舟云学术

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“High” antiretroviral deintensification, a strategy to avoid drug interactions and unfavourable long-term effects of HAART

Published:2018-06-19 Issue:10 Volume:50 Page:788-790
ISSN:2374-4235
Container-title:Infectious Diseases
language:en
Short-container-title:Infectious Diseases

Author:

Lanzafame Massimiliano¹,Piacentini Daniela²,Lattuada Emanuela²,Rizzardo Sebastiano²,Chiesi Sheila²,Vento Sandro³

Affiliation:

1. Diagnosis and Therapy of HIV Infection Unit, G.B. Rossi University Hospital, Verona, CAP, Italy;

2. Infectious Diseases Unit, G.B. Rossi University Hospital, Verona, CAP , Italy;

3. Department of Medicine, School of Medicine, Nazarbayev University, Astana, Kazakhstan

Publisher

Informa UK Limited

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/23744235.2018.1482420

Reference9 articles.

1. Low-dose versus standard-dose ritonavir-boosted atazanavir in virologically suppressed Thai adults with HIV (LASA): a randomised, open-label, non-inferiority trial

2. Virological Efficacy of a Reduced Dose of Nevirapine in a Small Cohort of Suppressed HIV-1–Infected Patients

3. Efavirenz dose reduction in HIV-infected patients

4. A 96‐Week Comparison of Lopinavir‐Ritonavir Combination Therapy Followed by Lopinavir‐Ritonavir Monotherapy versus Efavirenz Combination Therapy

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Phomoarcherin B as a novel HIV-1 reverse transcriptase RNase H activity inhibitor: conclusions from comprehensive computational analysis;2021-09-10

2. ‘High’ antiretroviral deintensification strategy and cellular HIV DNA levels;Journal of Chemotherapy;2019-12-06

3. Dolutegravir monotherapy: an option for highly adherent HIV1-infected naive patients with relatively low zenith HIV-RNA?;Infectious Diseases;2018-10-14

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