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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.
Source: Journal of Neurochemistry. Conference titles: Biennial Meeting of the International Society for Neurochemistry. Unidade: FM
Subjects: 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: 21 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. 21 ] 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. 21 ] 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.
Source: Brain Pathology. Conference titles: International Congress of Neuropathology. Unidade: FM
Subjects: 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: 21 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. 21 ] 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. 21 ] 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.
Source: Brain Pathology. Conference titles: International Congress of Neuropathology. Unidade: FM
Subjects: 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: 21 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. 21 ] 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. 21 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
Artigo de periodico
Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old age (2013)
Souza, C. C. R.; Dombroski, Thaís Caroline Dallabona; Machado, Hélio Rubens; Oliveira, R. S.; Rocha, L. B.; Rodrigues, A. R. A.; Serafini, Luciano Neder; Chimelli, L.; Corrêa, V. M. A.; Larson, Roy Edward; Martins, Antonio Roberto
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: MIOSINA, CEREBELO (HUMANO), ENVELHECIMENTO, IMUNOHISTOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, C. C. R. et al. Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old age. Brazilian Journal of Medical and Biological Research, v. 46, n. 2, p. 164-170, 2013Tradução . . Disponível em: https://doi.org/10.1590/1414-431X20122627. Acesso em: 21 out. 2025.
APA
Souza, C. C. R., Dombroski, T. C. D., Machado, H. R., Oliveira, R. S., Rocha, L. B., Rodrigues, A. R. A., et al. (2013). Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old age. Brazilian Journal of Medical and Biological Research, 46( 2), 164-170. doi:10.1590/1414-431X20122627
NLM
Souza CCR, Dombroski TCD, Machado HR, Oliveira RS, Rocha LB, Rodrigues ARA, Serafini LN, Chimelli L, Corrêa VMA, Larson RE, Martins AR. Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old age [Internet]. Brazilian Journal of Medical and Biological Research. 2013 ; 46( 2): 164-170.[citado 2025 out. 21 ] Available from: https://doi.org/10.1590/1414-431X20122627
Vancouver
Souza CCR, Dombroski TCD, Machado HR, Oliveira RS, Rocha LB, Rodrigues ARA, Serafini LN, Chimelli L, Corrêa VMA, Larson RE, Martins AR. Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old age [Internet]. Brazilian Journal of Medical and Biological Research. 2013 ; 46( 2): 164-170.[citado 2025 out. 21 ] Available from: https://doi.org/10.1590/1414-431X20122627
Trabalho de evento-resumo periodico
Multineuropatia hansenica limitada a um membro (2006)
Barreira, Amilton Antunes; Marques, Vanessa Daccach; Chimelli, L.; Marques Júnior, Wilson
Source: Arquivos de Neuro-Psiquiatria. Conference titles: Congresso Brasileiro de Neurologia. Unidade: FMRP
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARREIRA, Amilton Antunes et al. Multineuropatia hansenica limitada a um membro. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 2006
APA
Barreira, A. A., Marques, V. D., Chimelli, L., & Marques Júnior, W. (2006). Multineuropatia hansenica limitada a um membro. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Barreira AA, Marques VD, Chimelli L, Marques Júnior W. Multineuropatia hansenica limitada a um membro. Arquivos de Neuro-Psiquiatria. 2006 ; 64 221.[citado 2025 out. 21 ]
Vancouver
Barreira AA, Marques VD, Chimelli L, Marques Júnior W. Multineuropatia hansenica limitada a um membro. Arquivos de Neuro-Psiquiatria. 2006 ; 64 221.[citado 2025 out. 21 ]
Artigo de periodico
Efeccts of chronic heart disease on skeletal muscle fiber size (2005)
Mattiello-Sverzut, Ana Cláudia; Chimelli, L.; Teixeira, S.; Pierre, M.; Oliveira, L.
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: MORFOMETRIA, MÚSCULOS, CARDIOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MATTIELLO-SVERZUT, Ana Cláudia et al. Efeccts of chronic heart disease on skeletal muscle fiber size. Brazilian Journal of Medical and Biological Research, v. 38, n. 2, p. 303-307, 2005Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2005000200019. Acesso em: 21 out. 2025.
APA
Mattiello-Sverzut, A. C., Chimelli, L., Teixeira, S., Pierre, M., & Oliveira, L. (2005). Efeccts of chronic heart disease on skeletal muscle fiber size. Brazilian Journal of Medical and Biological Research, 38( 2), 303-307. doi:10.1590/s0100-879x2005000200019
NLM
Mattiello-Sverzut AC, Chimelli L, Teixeira S, Pierre M, Oliveira L. Efeccts of chronic heart disease on skeletal muscle fiber size [Internet]. Brazilian Journal of Medical and Biological Research. 2005 ; 38( 2): 303-307.[citado 2025 out. 21 ] Available from: https://doi.org/10.1590/s0100-879x2005000200019
Vancouver
Mattiello-Sverzut AC, Chimelli L, Teixeira S, Pierre M, Oliveira L. Efeccts of chronic heart disease on skeletal muscle fiber size [Internet]. Brazilian Journal of Medical and Biological Research. 2005 ; 38( 2): 303-307.[citado 2025 out. 21 ] Available from: https://doi.org/10.1590/s0100-879x2005000200019
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.
Source: Neurogenetics. Unidade: FM
Subjects: 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: 21 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. 21 ] 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. 21 ] Available from: https://doi.org/10.1007/s100480100114

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