Filtros : "FCF" "CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA" "Schramm, Simone Grigoleto" Removidos: "Financiado pela Brazilian Society of Cardiology" "Faculdade de Ciências da Saúde IGESP. São Paulo, SP" "Molecular Probes, Inc., Eugene, USA" "Universidad Nacional de Trujillo Juan Pablo II - Peru" "Universidade de São Paulo - USP" Limpar

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  • Source: Clinical Therapeutics. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, FARMACOCINÉTICA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA

    Acesso à fonteHow to cite
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    • ABNT

      SILVA, Marina de Freitas et al. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers. Clinical Therapeutics, v. 32, n. 4, p. 758-765, 2010Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf. Acesso em: 29 jun. 2024.
    • APA

      Silva, M. de F., Schramm, S. G., Kano, E. K., Koono, E. E. M., Porta, V., & Serra, C. H. dos R. (2010). Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers. Clinical Therapeutics, 32( 4), 758-765. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
    • NLM

      Silva M de F, Schramm SG, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers [Internet]. Clinical Therapeutics. 2010 ; 32( 4): 758-765.[citado 2024 jun. 29 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
    • Vancouver

      Silva M de F, Schramm SG, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers [Internet]. Clinical Therapeutics. 2010 ; 32( 4): 758-765.[citado 2024 jun. 29 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
  • Source: Journal of Chromatographic Science. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ANTIBIÓTICOS

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    • ABNT

      SILVA, Marina et al. Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science, v. 47, p. 781-784, 2009Tradução . . Acesso em: 29 jun. 2024.
    • APA

      Silva, M., Schramm, S. G., Kano, E. K., Porta, V., & Serra, C. H. dos R. (2009). Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science, 47, 781-784.
    • NLM

      Silva M, Schramm SG, Kano EK, Porta V, Serra CH dos R. Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science. 2009 ; 47 781-784.[citado 2024 jun. 29 ]
    • Vancouver

      Silva M, Schramm SG, Kano EK, Porta V, Serra CH dos R. Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science. 2009 ; 47 781-784.[citado 2024 jun. 29 ]
  • Source: Latin American Journal of Pharmacy. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ZIDOVUDINA

    Acesso à fonteHow to cite
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    • ABNT

      SOUZA, Jacqueline de et al. Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet. Latin American Journal of Pharmacy, v. 28, n. 3, p. 433-437, 2009Tradução . . Disponível em: http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf. Acesso em: 29 jun. 2024.
    • APA

      Souza, J. de, Kano, E. K., Koono, E. E. M., Schramm, S. G., Porta, V., & Storpirtis, S. (2009). Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet. Latin American Journal of Pharmacy, 28( 3), 433-437. Recuperado de http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf
    • NLM

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet [Internet]. Latin American Journal of Pharmacy. 2009 ; 28( 3): 433-437.[citado 2024 jun. 29 ] Available from: http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf
    • Vancouver

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet [Internet]. Latin American Journal of Pharmacy. 2009 ; 28( 3): 433-437.[citado 2024 jun. 29 ] Available from: http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf

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