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Trabalho de evento-resumo periodico
Human prion diseases in brazil (2015)
Landemberger, M. C.; Machado, C.; Smid, J.; Gomes, H.; Chimelli, L.; Canedo, N.; Rosemberg, S.; Nitrini, R.; Martins, V.
Fonte: Journal of Neurochemistry. Nome do evento: Biennial Meeting of the International Society for Neurochemistry. Unidade: FM
Assuntos: DEMÊNCIA, DOENÇAS NEURODEGENERATIVAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LANDEMBERGER, M. C. et al. Human prion diseases in brazil. Journal of Neurochemistry. Oxford: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/jnc.13188/epdf. Acesso em: 25 out. 2025. , 2015
APA
Landemberger, M. C., Machado, C., Smid, J., Gomes, H., Chimelli, L., Canedo, N., et al. (2015). Human prion diseases in brazil. Journal of Neurochemistry. Oxford: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1111/jnc.13188/epdf
NLM
Landemberger MC, Machado C, Smid J, Gomes H, Chimelli L, Canedo N, Rosemberg S, Nitrini R, Martins V. Human prion diseases in brazil [Internet]. Journal of Neurochemistry. 2015 ; 134 201 abstr. MTU11-22.[citado 2025 out. 25 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/jnc.13188/epdf
Vancouver
Landemberger MC, Machado C, Smid J, Gomes H, Chimelli L, Canedo N, Rosemberg S, Nitrini R, Martins V. Human prion diseases in brazil [Internet]. Journal of Neurochemistry. 2015 ; 134 201 abstr. MTU11-22.[citado 2025 out. 25 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/jnc.13188/epdf
Trabalho de evento-resumo periodico
Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene (2014)
Smid, J.; Landemberger, M. C.; Martins, V. R.; Schultz, R. R.; Rosemberg. S.; Chimelli, L.; Nitrini, R.
Fonte: Brain Pathology. Nome do evento: International Congress of Neuropathology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, FENÓTIPOS, FAMÍLIA, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SMID, J. et al. Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf. Acesso em: 25 out. 2025. , 2014
APA
Smid, J., Landemberger, M. C., Martins, V. R., Schultz, R. R., Rosemberg. S.,, Chimelli, L., & Nitrini, R. (2014). Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf
NLM
Smid J, Landemberger MC, Martins VR, Schultz RR, Rosemberg. S., Chimelli L, Nitrini R. Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene [Internet]. Brain Pathology. 2014 ; 24 16.[citado 2025 out. 25 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf
Vancouver
Smid J, Landemberger MC, Martins VR, Schultz RR, Rosemberg. S., Chimelli L, Nitrini R. Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene [Internet]. Brain Pathology. 2014 ; 24 16.[citado 2025 out. 25 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf
Trabalho de evento-resumo periodico
Human prion diseases in Brazil (2014)
Landemberger, M. C.; Machado, C. F.; Smid, J.; Gomes, H. R.; Chimelli, L.; Rosemberg. S.; Nitrini, R.; Martins, V. R.
Fonte: Brain Pathology. Nome do evento: International Congress of Neuropathology. Unidade: FM
Assuntos: DOENÇA DE PRION, MUTAÇÃO GENÉTICA, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LANDEMBERGER, M. C. et al. Human prion diseases in Brazil. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf. Acesso em: 25 out. 2025. , 2014
APA
Landemberger, M. C., Machado, C. F., Smid, J., Gomes, H. R., Chimelli, L., Rosemberg. S.,, et al. (2014). Human prion diseases in Brazil. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
NLM
Landemberger MC, Machado CF, Smid J, Gomes HR, Chimelli L, Rosemberg. S., Nitrini R, Martins VR. Human prion diseases in Brazil [Internet]. Brain Pathology. 2014 ; 24 81.[citado 2025 out. 25 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
Vancouver
Landemberger MC, Machado CF, Smid J, Gomes HR, Chimelli L, Rosemberg. S., Nitrini R, Martins VR. Human prion diseases in Brazil [Internet]. Brain Pathology. 2014 ; 24 81.[citado 2025 out. 25 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
Artigo de periodico
Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents (2001)
Kösel, S.; Grasbon-Frodl, E. M.; Arima, K.; Chimelli, L.; Hahn, M.; Hashizume, Y.; Hulette, C.; Ikeda, K.; Jacobsen, P. F.; Jones, M.; Kobayashi, M.; Love, S.; Mizutani, T.; Rosemberg, Sergio; Sasaki, A.; Smith, T. W.; Takahashi, H.; Vortmeyer, A. O.
Fonte: Neurogenetics. Unidade: FM
Assuntos: DNA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, DNA MITOCONDRIAL, REAÇÃO EM CADEIA POR POLIMERASE, ULTRAFILTRAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KÖSEL, S. et al. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents. Neurogenetics, v. 3, p. 163-170, 2001Tradução . . Disponível em: https://doi.org/10.1007/s100480100114. Acesso em: 25 out. 2025.
APA
Kösel, S., Grasbon-Frodl, E. M., Arima, K., Chimelli, L., Hahn, M., Hashizume, Y., et al. (2001). Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents. Neurogenetics, 3, 163-170. doi:10.1007/s100480100114
NLM
Kösel S, Grasbon-Frodl EM, Arima K, Chimelli L, Hahn M, Hashizume Y, Hulette C, Ikeda K, Jacobsen PF, Jones M, Kobayashi M, Love S, Mizutani T, Rosemberg S, Sasaki A, Smith TW, Takahashi H, Vortmeyer AO. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents [Internet]. Neurogenetics. 2001 ; 3 163-170.[citado 2025 out. 25 ] Available from: https://doi.org/10.1007/s100480100114
Vancouver
Kösel S, Grasbon-Frodl EM, Arima K, Chimelli L, Hahn M, Hashizume Y, Hulette C, Ikeda K, Jacobsen PF, Jones M, Kobayashi M, Love S, Mizutani T, Rosemberg S, Sasaki A, Smith TW, Takahashi H, Vortmeyer AO. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents [Internet]. Neurogenetics. 2001 ; 3 163-170.[citado 2025 out. 25 ] Available from: https://doi.org/10.1007/s100480100114

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