Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Science and Pharmaceutical Technology Meeting of the Pharmaceutical Sciences Faculty of the University of São Paulo. Unidade: FM
Subjects: BIOEQUIVALÊNCIA, FARMACOCINÉTICA CLÍNICA, VALIDAÇÃO DE MODELOS, PLASMA (ANÁLISE QUANTITATIVA), RESUMOS
ABNT
BELOTTO, Karisa Cristina Rodrigues et al. Validation of LC-MS/MS method for the quantification of risperidone and its active metabolite 9-OH-risperidone in human plasma and its application in a bioequivalence study. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2010APA
Belotto, K. C. R., Raposo, N. R. B., Ferreira, A. S., & Gattaz, W. F. (2010). Validation of LC-MS/MS method for the quantification of risperidone and its active metabolite 9-OH-risperidone in human plasma and its application in a bioequivalence study. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo.NLM
Belotto KCR, Raposo NRB, Ferreira AS, Gattaz WF. Validation of LC-MS/MS method for the quantification of risperidone and its active metabolite 9-OH-risperidone in human plasma and its application in a bioequivalence study. Brazilian Journal of Pharmaceutical Sciences. 2010 ; 46 11 res. FCF018.[citado 2024 out. 17 ]Vancouver
Belotto KCR, Raposo NRB, Ferreira AS, Gattaz WF. Validation of LC-MS/MS method for the quantification of risperidone and its active metabolite 9-OH-risperidone in human plasma and its application in a bioequivalence study. Brazilian Journal of Pharmaceutical Sciences. 2010 ; 46 11 res. FCF018.[citado 2024 out. 17 ]