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Artigo de periodico
Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report (2001)
Yacubian, Elza Márcia T.; Rosemberg, Sérgio; Garrido Neto, Theodomiro L.; Marie, Suely Kazue Nagahashi; Valério, Rosa M. F.; Jorge, Carmen Lisa
Source: Journal of Child Neurology. Unidade: FM
Subjects: NEUROLOGIA, CRIANÇAS
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ABNT
YACUBIAN, Elza Márcia T. et al. Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology, v. 16, n. 05, p. 374-377, 2001Tradução . . Acesso em: 12 nov. 2024.
APA
Yacubian, E. M. T., Rosemberg, S., Garrido Neto, T. L., Marie, S. K. N., Valério, R. M. F., & Jorge, C. L. (2001). Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology, 16( 05), 374-377.
NLM
Yacubian EMT, Rosemberg S, Garrido Neto TL, Marie SKN, Valério RMF, Jorge CL. Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology. 2001 ; 16( 05): 374-377.[citado 2024 nov. 12 ]
Vancouver
Yacubian EMT, Rosemberg S, Garrido Neto TL, Marie SKN, Valério RMF, Jorge CL. Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology. 2001 ; 16( 05): 374-377.[citado 2024 nov. 12 ]
Artigo de periodico
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases (2000)
Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Gobbo, L. F.; Gurgel, J. E. P.; Carvalho, M. S.; Resende, M. B. D.; Espindola, A. A.; Zatz, Mayana ; Diament, Aron Judka
Source: Journal of Child Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
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ABNT
REED, Umbertina Conti et al. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology, v. 15, n. 3, p. 172-8, 2000Tradução . . Acesso em: 12 nov. 2024.
APA
Reed, U. C., Marie, S. K. N., Vainzof, M., Gobbo, L. F., Gurgel, J. E. P., Carvalho, M. S., et al. (2000). Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology, 15( 3), 172-8.
NLM
Reed UC, Marie SKN, Vainzof M, Gobbo LF, Gurgel JEP, Carvalho MS, Resende MBD, Espindola AA, Zatz M, Diament AJ. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology. 2000 ; 15( 3): 172-8.[citado 2024 nov. 12 ]
Vancouver
Reed UC, Marie SKN, Vainzof M, Gobbo LF, Gurgel JEP, Carvalho MS, Resende MBD, Espindola AA, Zatz M, Diament AJ. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology. 2000 ; 15( 3): 172-8.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy (1999)
Omuro, Antonio M. P; Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Carvalho, Mary S; Rusticci, Monica; Fernandes, Simone A
Source: Neurology. Conference titles: American Academy of Neurology Annual Meeting. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
OMURO, Antonio M. P et al. Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy. Neurology. Canada: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1999
APA
Omuro, A. M. P., Reed, U. C., Marie, S. K. N., Vainzof, M., Carvalho, M. S., Rusticci, M., & Fernandes, S. A. (1999). Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy. Neurology. Canada: Faculdade de Medicina, Universidade de São Paulo.
NLM
Omuro AMP, Reed UC, Marie SKN, Vainzof M, Carvalho MS, Rusticci M, Fernandes SA. Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy. Neurology. 1999 ; 52( 06): A51.[citado 2024 nov. 12 ]
Vancouver
Omuro AMP, Reed UC, Marie SKN, Vainzof M, Carvalho MS, Rusticci M, Fernandes SA. Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy. Neurology. 1999 ; 52( 06): A51.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy (1999)
Vainzof, Mariz ; Rusticci, Monica S; Marie, Suely Kazue Nagahashi; Zatz, Mayana ; Tsanaclis, Ana Maria Crous; Silva, Helga Cristina Almeida da
Source: Neurology. Conference titles: American Academy of Neurology Annual Meeting. Unidades: FM, IB
Assunto: NEUROLOGIA
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ABNT
VAINZOF, Mariz et al. Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy. Neurology. Canada: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1999
APA
Vainzof, M., Rusticci, M. S., Marie, S. K. N., Zatz, M., Tsanaclis, A. M. C., & Silva, H. C. A. da. (1999). Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy. Neurology. Canada: Faculdade de Medicina, Universidade de São Paulo.
NLM
Vainzof M, Rusticci MS, Marie SKN, Zatz M, Tsanaclis AMC, Silva HCA da. Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy. Neurology. 1999 ; 52( 06): A331.[citado 2024 nov. 12 ]
Vancouver
Vainzof M, Rusticci MS, Marie SKN, Zatz M, Tsanaclis AMC, Silva HCA da. Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy. Neurology. 1999 ; 52( 06): A331.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Rods proteic-constituition and muscle fiber maturation in nemaline myopathy (1999)
Gurgel, Juliana E. P; Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Zatz, Mayana ; Vainzof, Mariz ; Carvalho, Mary
Source: Neurology. Conference titles: American Academy of Neurology Annual Meeting. Unidades: FM, IB
Assunto: NEUROLOGIA
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ABNT
GURGEL, Juliana E. P et al. Rods proteic-constituition and muscle fiber maturation in nemaline myopathy. Neurology. Canada: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1999
APA
Gurgel, J. E. P., Reed, U. C., Marie, S. K. N., Zatz, M., Vainzof, M., & Carvalho, M. (1999). Rods proteic-constituition and muscle fiber maturation in nemaline myopathy. Neurology. Canada: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gurgel JEP, Reed UC, Marie SKN, Zatz M, Vainzof M, Carvalho M. Rods proteic-constituition and muscle fiber maturation in nemaline myopathy. Neurology. 1999 ; 52( 06): A332.[citado 2024 nov. 12 ]
Vancouver
Gurgel JEP, Reed UC, Marie SKN, Zatz M, Vainzof M, Carvalho M. Rods proteic-constituition and muscle fiber maturation in nemaline myopathy. Neurology. 1999 ; 52( 06): A332.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy (1993)
Passos-Bueno, Maria Rita ; Cerqueira, A; Takata, R I; Pavanello, R C M; Eggers, S.; Marie, Suely Kazue Nagahashi; Levy, J A; Zatz, Mayana
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
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ABNT
PASSOS-BUENO, Maria Rita et al. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Passos-Bueno, M. R., Cerqueira, A., Takata, R. I., Pavanello, R. C. M., Eggers, S., Marie, S. K. N., et al. (1993). Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Passos-Bueno MR, Cerqueira A, Takata RI, Pavanello RCM, Eggers S, Marie SKN, Levy JA, Zatz M. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 nov. 12 ]
Vancouver
Passos-Bueno MR, Cerqueira A, Takata RI, Pavanello RCM, Eggers S, Marie SKN, Levy JA, Zatz M. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Stick-man: report of five cases of favorable evolution (1993)
Marie, Suely Kazue Nagahashi; Carvalho, A A S; Reed, Umbertina Conti; Carvalho, M. S.; Salum, P; Levy, J A
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
MARIE, Suely Kazue Nagahashi et al. Stick-man: report of five cases of favorable evolution. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Marie, S. K. N., Carvalho, A. A. S., Reed, U. C., Carvalho, M. S., Salum, P., & Levy, J. A. (1993). Stick-man: report of five cases of favorable evolution. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Marie SKN, Carvalho AAS, Reed UC, Carvalho MS, Salum P, Levy JA. Stick-man: report of five cases of favorable evolution. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s160.[citado 2024 nov. 12 ]
Vancouver
Marie SKN, Carvalho AAS, Reed UC, Carvalho MS, Salum P, Levy JA. Stick-man: report of five cases of favorable evolution. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s160.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Antiphospholipid antibodies (apl) and ischemic stroke in the young (1993)
Tinone, G; Yamamoto, F I; Comerlatti, L R; Scaff, Milberto
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
TINONE, G et al. Antiphospholipid antibodies (apl) and ischemic stroke in the young. Canadian Journal of Neurological Sciences. Vancouver: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Tinone, G., Yamamoto, F. I., Comerlatti, L. R., & Scaff, M. (1993). Antiphospholipid antibodies (apl) and ischemic stroke in the young. Canadian Journal of Neurological Sciences. Vancouver: Faculdade de Medicina, Universidade de São Paulo.
NLM
Tinone G, Yamamoto FI, Comerlatti LR, Scaff M. Antiphospholipid antibodies (apl) and ischemic stroke in the young. Canadian Journal of Neurological Sciences. 1993 ;20( supl.4): s245.[citado 2024 nov. 12 ]
Vancouver
Tinone G, Yamamoto FI, Comerlatti LR, Scaff M. Antiphospholipid antibodies (apl) and ischemic stroke in the young. Canadian Journal of Neurological Sciences. 1993 ;20( supl.4): s245.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Aids: a csf laboratory experience on 610 cases in a 8 year time period (1993)
Livramento, J A; Machado, Luís dos Ramos; Nobrega, J P S; Spina Franca, A
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
LIVRAMENTO, J A et al. Aids: a csf laboratory experience on 610 cases in a 8 year time period. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Livramento, J. A., Machado, L. dos R., Nobrega, J. P. S., & Spina Franca, A. (1993). Aids: a csf laboratory experience on 610 cases in a 8 year time period. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Livramento JA, Machado L dos R, Nobrega JPS, Spina Franca A. Aids: a csf laboratory experience on 610 cases in a 8 year time period. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s118.[citado 2024 nov. 12 ]
Vancouver
Livramento JA, Machado L dos R, Nobrega JPS, Spina Franca A. Aids: a csf laboratory experience on 610 cases in a 8 year time period. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s118.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families (1993)
Passos-Bueno, Maria Rita ; Wijmenga, C; Takata, R I; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Pavanello, R C M; Hewitt, J E; Bakker, E; Carvalho, A A S; Akiyama, J; Frants, R R
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
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ABNT
PASSOS-BUENO, Maria Rita et al. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Passos-Bueno, M. R., Wijmenga, C., Takata, R. I., Marie, S. K. N., Vainzof, M., Pavanello, R. C. M., et al. (1993). Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho AAS, Akiyama J, Frants RR. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 nov. 12 ]
Vancouver
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho AAS, Akiyama J, Frants RR. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Central nervous system paracoccidioidomycosis (1993)
Nobrega, J P S; Leite Neto, A M; Livramento, J A; Machado, Luís dos Ramos; Spina Franca, A
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
NOBREGA, J P S et al. Central nervous system paracoccidioidomycosis. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Nobrega, J. P. S., Leite Neto, A. M., Livramento, J. A., Machado, L. dos R., & Spina Franca, A. (1993). Central nervous system paracoccidioidomycosis. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Nobrega JPS, Leite Neto AM, Livramento JA, Machado L dos R, Spina Franca A. Central nervous system paracoccidioidomycosis. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s40.[citado 2024 nov. 12 ]
Vancouver
Nobrega JPS, Leite Neto AM, Livramento JA, Machado L dos R, Spina Franca A. Central nervous system paracoccidioidomycosis. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s40.[citado 2024 nov. 12 ]
Trabalho de evento-resumo periodico
Vasculitis of the central nervous system: a survey of 20 cases (1993)
Yamamoto, F I; Marchiori, P E; Tinone, G; Scaff, Milberto
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
YAMAMOTO, F I et al. Vasculitis of the central nervous system: a survey of 20 cases. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1993
APA
Yamamoto, F. I., Marchiori, P. E., Tinone, G., & Scaff, M. (1993). Vasculitis of the central nervous system: a survey of 20 cases. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Yamamoto FI, Marchiori PE, Tinone G, Scaff M. Vasculitis of the central nervous system: a survey of 20 cases. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): 5243.[citado 2024 nov. 12 ]
Vancouver
Yamamoto FI, Marchiori PE, Tinone G, Scaff M. Vasculitis of the central nervous system: a survey of 20 cases. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): 5243.[citado 2024 nov. 12 ]

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