Cellular prion protein: implications in seizure and epilepsy (2002)
- Authors:
- USP affiliated authors: CARLOTTI JUNIOR, CARLOS GILBERTO - FMRP ; SAKAMOTO, AMERICO CEIKI - FMRP ; BRENTANI, RICARDO RENZO - FM
- Unidades: FMRP; FM
- Assunto: EPILEPSIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Cellular and Molecular Neurobiology
- ISSN: 0272-4340
- Volume/Número/Paginação/Ano: v. 22, n. 3, p. 249-257, 2002
-
ABNT
WALZ, Roger et al. Cellular prion protein: implications in seizure and epilepsy. Cellular and Molecular Neurobiology, v. 22, n. 3, p. 249-257, 2002Tradução . . Acesso em: 10 fev. 2026. -
APA
Walz, R., Castro, R. M. R. P. S., Velasco, T. R., Carlotti Júnior, C. G., Sakamoto, A. C., Brentani, R. R., & Martins, V. R. (2002). Cellular prion protein: implications in seizure and epilepsy. Cellular and Molecular Neurobiology, 22( 3), 249-257. -
NLM
Walz R, Castro RMRPS, Velasco TR, Carlotti Júnior CG, Sakamoto AC, Brentani RR, Martins VR. Cellular prion protein: implications in seizure and epilepsy. Cellular and Molecular Neurobiology. 2002 ; 22( 3): 249-257.[citado 2026 fev. 10 ] -
Vancouver
Walz R, Castro RMRPS, Velasco TR, Carlotti Júnior CG, Sakamoto AC, Brentani RR, Martins VR. Cellular prion protein: implications in seizure and epilepsy. Cellular and Molecular Neurobiology. 2002 ; 22( 3): 249-257.[citado 2026 fev. 10 ] - 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
- Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein
- On the prognostic value of ictal EEG patterns in temporal lobe epilepsy surgery: a cohort study
- Nasu-Hakola disease (Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy-PLOSL): Adementia associated with bone cystic lesions. From clinical to genetic and molecular aspects
- Atypical neuropsychological profiles and cognitive outcome in mesial temporal lobe epilepsy
- Suppression of obsessive-compulsive symptoms after epilepsy surgery
- Cortical malformations are associated with a rare polymorphism of cellular prion protein
- Human cellular prion protein gene variant alleles are associated with intractable symptomatic epilepsies
- Do psychiatric comorbidities predict postoperative seizure outcome in temporal lobe epilepsy surgery?
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