Risk of Selecting De Novo Drug-Resistance Mutations during Structured Treatment Interruptions in Patients with Chronic HIV Infection-Reference-Cited by-同舟云学术

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Risk of Selecting De Novo Drug-Resistance Mutations during Structured Treatment Interruptions in Patients with Chronic HIV Infection

Published:2005-09-15 Issue:6 Volume:41 Page:883-890
ISSN:1058-4838
Container-title:Clinical Infectious Diseases
language:en
Short-container-title:Clinical Infectious Diseases

Author:

Arnedo-Valero M.,Garcia F.,Gil C.,Guila T.,Fumero E.,Castro P.,Blanco J. L.,Miro J. M.,Pumarola T.,Gatell J. M.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Link

http://academic.oup.com/cid/article-pdf/41/6/883/5930139/41-6-883.pdf

Reference24 articles.

1. Treatment with Indinavir, Zidovudine, and Lamivudine in Adults with Human Immunodeficiency Virus Infection and Prior Antiretroviral Therapy

2. Declining Morbidity and Mortality among Patients with Advanced Human Immunodeficiency Virus Infection

3. Latent infection of CD4+ T cells provides a mechanism for lifelong persistence of HIV-1, even in patients on effective combination therapy

4. Long-term follow-up studies confirm the stability of the latent reservoir for HIV-1 in resting CD4+ T cells

5. Risk of lipodystrophy in HIV-1-infected patients treated with protease inhibitors: a prospective cohort study

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2. High rate of long-term clinical events after antiretroviral therapy resumption in HIV-positive patients exposed to antiretroviral therapy interruption;AIDS;2021-08-20

3. Effect of innate and adaptive immune mechanisms on treatment regimens in an AIDS-related Kaposi's Sarcoma model;Journal of Biological Dynamics;2021-01-01

4. Antiretroviral Therapy Interruption (ATI) in HIV-1 Infected Patients Participating in Therapeutic Vaccine Trials: Surrogate Markers of Virological Response;Vaccines;2020-08-05

5. A comparison of machine learning techniques for classification of HIV patients with antiretroviral therapy-induced mitochondrial toxicity from those without mitochondrial toxicity;BMC Medical Research Methodology;2019-11-27

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