Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis (1999)
- Autores:
- Autores USP: LANCHOTE, VERA LUCIA - FCFRP ; SANTOS, SILVIA REGINA CAVANI JORGE - FCF ; BONATO, PIERINA SUELI - FCFRP
- Unidades: FCFRP; FCF
- DOI: 10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g
- Assuntos: FARMACOLOGIA; FARMACOCINÉTICA; METABOLISMO; CISTICERCOSE
- Idioma: Inglês
- Imprenta:
- Fonte:
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
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ABNT
MARQUES, Maria Paula da Costa et al. Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis. Chirality, v. 11, n. 3, p. 218-233, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g. Acesso em: 01 maio 2024. -
APA
Marques, M. P. da C., Takayanagui, O. M., Bonato, P. S., Santos, S. R. C. J., & Lanchote, V. L. (1999). Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis. Chirality, 11( 3), 218-233. doi:10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g -
NLM
Marques MP da C, Takayanagui OM, Bonato PS, Santos SRCJ, Lanchote VL. Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis [Internet]. Chirality. 1999 ; 11( 3): 218-233.[citado 2024 maio 01 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g -
Vancouver
Marques MP da C, Takayanagui OM, Bonato PS, Santos SRCJ, Lanchote VL. Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis [Internet]. Chirality. 1999 ; 11( 3): 218-233.[citado 2024 maio 01 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g - HPLC determination of the enantiomeric metabolites of mexiletine in human plasma: in vivo stereoselective hydroxylation
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Informações sobre o DOI: 10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g (Fonte: oaDOI API)
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