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: 10 fev. 2026. , 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 2026 fev. 10 ] -
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 2026 fev. 10 ] - Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein
- Cellular prion protein: implications in seizure and epilepsy
- Cortical malformations are associated with a rare polymorphism of cellular prion protein
- Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171
- High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC
- Posterior cortex epileptogenic lesions: clinical, electrophysiologic, imaging, surgical, pathological and outcome data
- Brain maturation and epilepsy onset in mesial temporal lobe epilepsy: a new look in an old taylor's hypothesis
- Postsurgical seizure outcome in non-hippocampal sclerosis temporal lobe epilepsy
- Accuracy of ictal SPECT in mesial temporal lobe epilepsy with bilateral interictal spikes
- "Prêmio cesare lombroso" acurácia do SPECT ictal em epilepsia temporal mesial associada 'a esclerose hipocampal
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
