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Trabalho de evento-resumo periodico
Prion protein mutation with clinical features similar to frontotemporal dementia and parkinsonism kinked to chromossome 17 (FTDP-17) (1999)
Silva, Luís Sidônio Teixeira da; Rosemberg, Sérgio; Caramelli, Paulo; Albrecht, Steffen; Iughetti, Paula; Passos-Bueno, Maria Rita ; Zatz, Mayana ; LeBlanc, Andrea; Nitrini, Ricardo
Source: Arquivos de Neuro-Psiquiatria. Conference titles: Reunião de Pesquisadores em Doenças de Alzheimer e Desordens Relacionadas. Unidades: FM, IB
Assunto: PATOLOGIA
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ABNT
SILVA, Luís Sidônio Teixeira da et al. Prion protein mutation with clinical features similar to frontotemporal dementia and parkinsonism kinked to chromossome 17 (FTDP-17). Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 03 nov. 2024. , 1999
APA
Silva, L. S. T. da, Rosemberg, S., Caramelli, P., Albrecht, S., Iughetti, P., Passos-Bueno, M. R., et al. (1999). Prion protein mutation with clinical features similar to frontotemporal dementia and parkinsonism kinked to chromossome 17 (FTDP-17). Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Silva LST da, Rosemberg S, Caramelli P, Albrecht S, Iughetti P, Passos-Bueno MR, Zatz M, LeBlanc A, Nitrini R. Prion protein mutation with clinical features similar to frontotemporal dementia and parkinsonism kinked to chromossome 17 (FTDP-17). Arquivos de Neuro-Psiquiatria. 1999 ; 57 56.[citado 2024 nov. 03 ]
Vancouver
Silva LST da, Rosemberg S, Caramelli P, Albrecht S, Iughetti P, Passos-Bueno MR, Zatz M, LeBlanc A, Nitrini R. Prion protein mutation with clinical features similar to frontotemporal dementia and parkinsonism kinked to chromossome 17 (FTDP-17). Arquivos de Neuro-Psiquiatria. 1999 ; 57 56.[citado 2024 nov. 03 ]
Parte de monografia/livro
Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease (1998)
Nitrini, Ricardo; Rosemberg, Sérgio; Passos-Bueno, Maria Rita ; Silva, Luís S Teixeira; Iughetti, Paula; Papadopoulos, Maria; Carrilho, P M; Caramelli, Paulo; Albrecht, Steffen; Zatz, Mayana ; LeBanc, Andréa
Source: Prions and brain diseases in animals and humans. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NITRINI, Ricardo et al. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. Prions and brain diseases in animals and humans. Tradução . New York: Plenum Press, 1998. . . Acesso em: 03 nov. 2024.
APA
Nitrini, R., Rosemberg, S., Passos-Bueno, M. R., Silva, L. S. T., Iughetti, P., Papadopoulos, M., et al. (1998). Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In Prions and brain diseases in animals and humans. New York: Plenum Press.
NLM
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBanc A. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In: Prions and brain diseases in animals and humans. New York: Plenum Press; 1998. [citado 2024 nov. 03 ]
Vancouver
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBanc A. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In: Prions and brain diseases in animals and humans. New York: Plenum Press; 1998. [citado 2024 nov. 03 ]
Artigo de periodico
Familial spongiform encephalopathy associated with a novel prion protein gene mutation (1997)
Nitrini, Ricardo; Rosemberg, Sérgio; Passos-Bueno, Maria Rita ; Silva, Luís S Teixeira; Iughetti, Paula; Papadopoulos, Maria; Carrilho, Paulo M; Caramelli, Paulo; Albrecht, Steffen; Zatz, Mayana ; Le Blanc, Andrea
Source: Annals of Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.1002/ana.410420203

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