Human cellular prion protein gene variant alleles are associated with intractable symptomatic epilepsies (2002)
- Authors:
- Walz, Roger
- Castro, Rosa M. R. P. S.
- Velasco, Tonicarlo R.
- Alexandre Júnior, Veriano
- Maciag, Paulo C.
- Wichert-Ana, Lauro
- Terra-Bustamante, Vera Cristina
- Leite, João Paulo
- Fernandes, R. M. F. Fernandes
- Marques Júnior, Wilson
- Machado, Hélio Rubens
- Carlotti Júnior, Carlos Gilberto
- Assirati Júnior, João Alberto
- Moura, Ricardo
- Cabalero, Otávio
- Sakamoto, Américo Ceiki
- Brentani, Ricardo Renzo
- USP affiliated authors: MARQUES JUNIOR, WILSON - FMRP ; MACHADO, HELIO RUBENS - FMRP ; CARLOTTI JUNIOR, CARLOS GILBERTO - FMRP ; SAKAMOTO, AMERICO CEIKI - FMRP ; BRENTANI, RICARDO RENZO - FM
- Unidades: FMRP; FM
- Assunto: EPILEPSIA
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Annual Meeting of the American Epilepsy Society
-
ABNT
WALZ, Roger et al. Human cellular prion protein gene variant alleles are associated with intractable symptomatic epilepsies. Epilepsia. Amsterdam: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2002 -
APA
Walz, R., Castro, R. M. R. P. S., Velasco, T. R., Alexandre Júnior, V., Maciag, P. C., Wichert-Ana, L., et al. (2002). Human cellular prion protein gene variant alleles are associated with intractable symptomatic epilepsies. Epilepsia. Amsterdam: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Walz R, Castro RMRPS, Velasco TR, Alexandre Júnior V, Maciag PC, Wichert-Ana L, Terra-Bustamante VC, Leite JP, Fernandes RMFF, Marques Júnior W, Machado HR, Carlotti Júnior CG, Assirati Júnior JA, Moura R, Cabalero O, Sakamoto AC, Brentani RR. Human cellular prion protein gene variant alleles are associated with intractable symptomatic epilepsies. Epilepsia. 2002 ; 43 278 res. 3.087.[citado 2024 abr. 24 ] -
Vancouver
Walz R, Castro RMRPS, Velasco TR, Alexandre Júnior V, Maciag PC, Wichert-Ana L, Terra-Bustamante VC, Leite JP, Fernandes RMFF, Marques Júnior W, Machado HR, Carlotti Júnior CG, Assirati Júnior JA, Moura R, Cabalero O, Sakamoto AC, Brentani RR. Human cellular prion protein gene variant alleles are associated with intractable symptomatic epilepsies. Epilepsia. 2002 ; 43 278 res. 3.087.[citado 2024 abr. 24 ] - Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein
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