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Volumn 175, Issue 4, 1997, Pages 966-970

High-dose nevirapine in previously untreated human immunodeficiency virus type 1-infected persons does not result in sustained suppression of viral replication

Author keywords

[No Author keywords available]

Indexed keywords

NEVIRAPINE;

EID: 16944364799     PISSN: 00221899     EISSN: None     Source Type: Journal    
DOI: 10.1086/514002     Document Type: Article
Times cited : (56)

References (15)
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  • 2
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    • Nevirapine resistance mutations of human immunodeficiency virus type I selected during therapy
    • Richman DD, Havlir D, Corbeil J, et al. Nevirapine resistance mutations of human immunodeficiency virus type I selected during therapy. J Virol 1994;68:1660-6.
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    • Alternating nevirapine and zidovudine treatment of human immunodeficiency virus type 1-infected persons does not prolong nevirapine activity
    • De Jong MD, Loewenthal M, Boucher CAB, et al. Alternating nevirapine and zidovudine treatment of human immunodeficiency virus type 1-infected persons does not prolong nevirapine activity. J Infect Dis 1994;169:1346-50.
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    • De Jong, M.D.1    Loewenthal, M.2    Boucher, C.A.B.3
  • 4
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    • High-dose nevirapine: Safety, pharmacokinetics, and antiviral effect in patients with human immunodeficiency virus infection
    • Havlir D, Cheeseman SH, McLaughlin M, et al. High-dose nevirapine: safety, pharmacokinetics, and antiviral effect in patients with human immunodeficiency virus infection. J Infect Dis 1995;171:537-45.
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  • 7
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    • A microtiter format point mutation assay: Application to the detection of drug resistance in human immunodefi-ciency virus type 1-infected patients treated with zidovudine
    • Kaye S, Loveday C, Tedder RS. A microtiter format point mutation assay: application to the detection of drug resistance in human immunodefi-ciency virus type 1-infected patients treated with zidovudine. J Med Virol 1992;37:241-6.
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    • Kaye, S.1    Loveday, C.2    Tedder, R.S.3
  • 8
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    • A rapid and sensitive HPLC-UV method for the quantitation of an anti-HIV agent, nevirapine and its solid-phase extractable metabolites in biological fluids
    • Jayaraj A, Alexander J, Price C. A rapid and sensitive HPLC-UV method for the quantitation of an anti-HIV agent, nevirapine and its solid-phase extractable metabolites in biological fluids. Pharm Res 1992;9:S334.
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    • A controlled trial of nevirapine plus zidovudine versus zidovudine alone in p24 antigenemic HIV-infected patients
    • Carr A, Vella S, De Jong MD, et al. A controlled trial of nevirapine plus zidovudine versus zidovudine alone in p24 antigenemic HIV-infected patients. AIDS 1996;10:635-41.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.