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Artigo de periodico
Criminal Behavior in Frontotemporal Dementia and Alzheimer Disease (2015)
Liljegren, Madeleine; Naasan, Georges; Temlett, Julia; Perry, David C.; Rankin, Katherine P.; Merrilees, Jennifer; Grinberg, Lea T.; Seeley, William W.; Englund, Elisabet; Miller,Bruce L.
Source: JAMA Neurology. Unidade: FM
Subjects: DEMÊNCIA, COMPORTAMENTO CRIMINAL, DOENÇA DE ALZHEIMER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LILJEGREN, Madeleine et al. Criminal Behavior in Frontotemporal Dementia and Alzheimer Disease. JAMA Neurology, v. 72, n. 3, p. 295-300, 2015Tradução . . Disponível em: https://doi.org/10.1001/jamaneurol.2014.3781. Acesso em: 21 out. 2025.
APA
Liljegren, M., Naasan, G., Temlett, J., Perry, D. C., Rankin, K. P., Merrilees, J., et al. (2015). Criminal Behavior in Frontotemporal Dementia and Alzheimer Disease. JAMA Neurology, 72( 3), 295-300. doi:10.1001/jamaneurol.2014.3781
NLM
Liljegren M, Naasan G, Temlett J, Perry DC, Rankin KP, Merrilees J, Grinberg LT, Seeley WW, Englund E, Miller BL. Criminal Behavior in Frontotemporal Dementia and Alzheimer Disease [Internet]. JAMA Neurology. 2015 ; 72( 3): 295-300.[citado 2025 out. 21 ] Available from: https://doi.org/10.1001/jamaneurol.2014.3781
Vancouver
Liljegren M, Naasan G, Temlett J, Perry DC, Rankin KP, Merrilees J, Grinberg LT, Seeley WW, Englund E, Miller BL. Criminal Behavior in Frontotemporal Dementia and Alzheimer Disease [Internet]. JAMA Neurology. 2015 ; 72( 3): 295-300.[citado 2025 out. 21 ] Available from: https://doi.org/10.1001/jamaneurol.2014.3781
Artigo de periodico
Progranulin Mutations as Risk Factors for Alzheimer Disease (2013)
Perry, David C.; Lehmann, Manja; Yokoyama, Jennifer S.; Karydas, Anna; Lee, Jason JiYong; Coppola, Giovanni; Grinberg, Lea T.; Geschwind, Dan; Seeley, William W.; Miller, Bruce L.; Rosen, Howard; Rabinovici, Gil
Source: JAMA Neurology. Unidade: FM
Subjects: FATORES DE RISCO, DOENÇAS NEURODEGENERATIVAS, DOENÇA DE ALZHEIMER, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERRY, David C. et al. Progranulin Mutations as Risk Factors for Alzheimer Disease. JAMA Neurology, v. 70, n. 6, p. 774-778, 2013Tradução . . Disponível em: https://doi.org/10.1001/2013.jamaneurol.393. Acesso em: 21 out. 2025.
APA
Perry, D. C., Lehmann, M., Yokoyama, J. S., Karydas, A., Lee, J. J. Y., Coppola, G., et al. (2013). Progranulin Mutations as Risk Factors for Alzheimer Disease. JAMA Neurology, 70( 6), 774-778. doi:10.1001/2013.jamaneurol.393
NLM
Perry DC, Lehmann M, Yokoyama JS, Karydas A, Lee JJY, Coppola G, Grinberg LT, Geschwind D, Seeley WW, Miller BL, Rosen H, Rabinovici G. Progranulin Mutations as Risk Factors for Alzheimer Disease [Internet]. JAMA Neurology. 2013 ; 70( 6): 774-778.[citado 2025 out. 21 ] Available from: https://doi.org/10.1001/2013.jamaneurol.393
Vancouver
Perry DC, Lehmann M, Yokoyama JS, Karydas A, Lee JJY, Coppola G, Grinberg LT, Geschwind D, Seeley WW, Miller BL, Rosen H, Rabinovici G. Progranulin Mutations as Risk Factors for Alzheimer Disease [Internet]. JAMA Neurology. 2013 ; 70( 6): 774-778.[citado 2025 out. 21 ] Available from: https://doi.org/10.1001/2013.jamaneurol.393
Artigo de periodico
Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review (2013)
Gurgel Giannetti, Juliana; Oliveira, Guilherme; Brasileiro Filho, Geraldo; Martins, Poliana; Vainzof, Mariz ; Hirano, Michio
Source: JAMA Neurology. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, ACONSELHAMENTO GENÉTICO, PROTEÍNAS MUSCULARES, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GURGEL GIANNETTI, Juliana et al. Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review. JAMA Neurology, v. 70, n. 2, p. 258-261, 2013Tradução . . Disponível em: https://doi.org/10.1001/jamaneurol.2013.595. Acesso em: 21 out. 2025.
APA
Gurgel Giannetti, J., Oliveira, G., Brasileiro Filho, G., Martins, P., Vainzof, M., & Hirano, M. (2013). Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review. JAMA Neurology, 70( 2), 258-261. doi:10.1001/jamaneurol.2013.595
NLM
Gurgel Giannetti J, Oliveira G, Brasileiro Filho G, Martins P, Vainzof M, Hirano M. Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review [Internet]. JAMA Neurology. 2013 ; 70( 2): 258-261.[citado 2025 out. 21 ] Available from: https://doi.org/10.1001/jamaneurol.2013.595
Vancouver
Gurgel Giannetti J, Oliveira G, Brasileiro Filho G, Martins P, Vainzof M, Hirano M. Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review [Internet]. JAMA Neurology. 2013 ; 70( 2): 258-261.[citado 2025 out. 21 ] Available from: https://doi.org/10.1001/jamaneurol.2013.595

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