Familial spongiform encephalopathy associated with a novel prion protein gene mutation (1997)
- Authors:
- USP affiliated authors: NITRINI, RICARDO - FM ; ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: FM; IB
- DOI: 10.1002/ana.410420203
- Assunto: NEUROLOGIA
- Language: Inglês
- Source:
- Título: Annals of Neurology
- Volume/Número/Paginação/Ano: v. 42, n. 2, p. 138-146, 1997
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
NITRINI, Ricardo et al. Familial spongiform encephalopathy associated with a novel prion protein gene mutation. Annals of Neurology, v. 42, n. 2, p. 138-146, 1997Tradução . . Disponível em: https://doi.org/10.1002/ana.410420203. Acesso em: 21 fev. 2026. -
APA
Nitrini, R., Rosemberg, S., Passos-Bueno, M. R., Silva, L. S. T., Iughetti, P., Papadopoulos, M., et al. (1997). Familial spongiform encephalopathy associated with a novel prion protein gene mutation. Annals of Neurology, 42( 2), 138-146. doi:10.1002/ana.410420203 -
NLM
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, Le Blanc A. Familial spongiform encephalopathy associated with a novel prion protein gene mutation [Internet]. Annals of Neurology. 1997 ; 42( 2): 138-146.[citado 2026 fev. 21 ] Available from: https://doi.org/10.1002/ana.410420203 -
Vancouver
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, Le Blanc A. Familial spongiform encephalopathy associated with a novel prion protein gene mutation [Internet]. Annals of Neurology. 1997 ; 42( 2): 138-146.[citado 2026 fev. 21 ] Available from: https://doi.org/10.1002/ana.410420203 - A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
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Informações sobre o DOI: 10.1002/ana.410420203 (Fonte: oaDOI API)
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