Filtros : "Gouvea, S. P" Limpar

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  • Source: Journal of the Peripheral Nervous System. Conference titles: Meeting of Peripheral Nerve Society. Unidade: FMRP

    Subjects: DOENÇAS DO SISTEMA NERVOSO, MUTAÇÃO GENÉTICA, FENÓTIPOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      TOMASELLI, P. J et al. Identification of five novel mutations in brazilian families with X-linked CMT. Journal of the Peripheral Nervous System. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/jns.12225. Acesso em: 09 out. 2024. , 2017
    • APA

      Tomaselli, P. J., Gouvea, S. P., Nyshyama, K. F. S., Nicolau Junior, N., Lourenço, C. M., & Marques Júnior, W. (2017). Identification of five novel mutations in brazilian families with X-linked CMT. Journal of the Peripheral Nervous System. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/jns.12225
    • NLM

      Tomaselli PJ, Gouvea SP, Nyshyama KFS, Nicolau Junior N, Lourenço CM, Marques Júnior W. Identification of five novel mutations in brazilian families with X-linked CMT [Internet]. Journal of the Peripheral Nervous System. 2017 ; 22 396.[citado 2024 out. 09 ] Available from: https://doi.org/10.1111/jns.12225
    • Vancouver

      Tomaselli PJ, Gouvea SP, Nyshyama KFS, Nicolau Junior N, Lourenço CM, Marques Júnior W. Identification of five novel mutations in brazilian families with X-linked CMT [Internet]. Journal of the Peripheral Nervous System. 2017 ; 22 396.[citado 2024 out. 09 ] Available from: https://doi.org/10.1111/jns.12225
  • Source: Journal of the Peripheral Nervous System. Conference titles: Meeting of Peripheral Nerve Society. Unidade: FMRP

    Subjects: DOENÇAS DO SISTEMA NERVOSO, MUTAÇÃO GENÉTICA, ATROFIA MUSCULAR

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ROCHA, A. M et al. Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort. Journal of the Peripheral Nervous System. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/jns.12225. Acesso em: 09 out. 2024. , 2017
    • APA

      Rocha, A. M., Tomaselli, P. J., Gouvea, S. P., Figueiredo, F. B., Lourenço, C. M., & Marques Júnior, W. (2017). Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort. Journal of the Peripheral Nervous System. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/jns.12225
    • NLM

      Rocha AM, Tomaselli PJ, Gouvea SP, Figueiredo FB, Lourenço CM, Marques Júnior W. Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort [Internet]. Journal of the Peripheral Nervous System. 2017 ; 22 367-368.[citado 2024 out. 09 ] Available from: https://doi.org/10.1111/jns.12225
    • Vancouver

      Rocha AM, Tomaselli PJ, Gouvea SP, Figueiredo FB, Lourenço CM, Marques Júnior W. Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort [Internet]. Journal of the Peripheral Nervous System. 2017 ; 22 367-368.[citado 2024 out. 09 ] Available from: https://doi.org/10.1111/jns.12225

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