ReP USP - Resultado da busca

Trabalho de evento-resumo
Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy (2007)
Ambrósio, Carlos Eduardo; Kerkis, I; Martins, D. S; Kerkis, A; Vanizof, M; Fonseca, S. A. S; Maranduba, C; Cabral, R. M; Peixoto, T. G; Morini, Adriana Caroprezo; Brólio, Roberto; Bertolini, L. R; Miglino, Maria Angélica; Zatz, Mayana
Source: Abstracts. Conference titles: International Federation of Placenta Association Meeting. Unidades: FMVZ, IB
Subjects: CÃES, CÉLULAS, DISTROFIA MUSCULAR ANIMAL
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ABNT
AMBRÓSIO, Carlos Eduardo et al. Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. 2007, Anais.. Kingston: Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, 2007. . Acesso em: 14 nov. 2024.
APA
Ambrósio, C. E., Kerkis, I., Martins, D. S., Kerkis, A., Vanizof, M., Fonseca, S. A. S., et al. (2007). Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. In Abstracts. Kingston: Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo.
NLM
Ambrósio CE, Kerkis I, Martins DS, Kerkis A, Vanizof M, Fonseca SAS, Maranduba C, Cabral RM, Peixoto TG, Morini AC, Brólio R, Bertolini LR, Miglino MA, Zatz M. Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. Abstracts. 2007 ;[citado 2024 nov. 14 ]
Vancouver
Ambrósio CE, Kerkis I, Martins DS, Kerkis A, Vanizof M, Fonseca SAS, Maranduba C, Cabral RM, Peixoto TG, Morini AC, Brólio R, Bertolini LR, Miglino MA, Zatz M. Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. Abstracts. 2007 ;[citado 2024 nov. 14 ]
Artigo de periodico
Calpainopathy: focus on a pediatric population (2003)
Kolski, H.; Edmonton, A. B.; Vajsar, J.; Paula, F de; Zatz, Mayana
Source: Journal of Child Neurology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
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ABNT
KOLSKI, H. et al. Calpainopathy: focus on a pediatric population. Journal of Child Neurology, v. 18, n. 3, p. 212, 2003Tradução . . Acesso em: 14 nov. 2024.
APA
Kolski, H., Edmonton, A. B., Vajsar, J., Paula, F. de, & Zatz, M. (2003). Calpainopathy: focus on a pediatric population. Journal of Child Neurology, 18( 3), 212.
NLM
Kolski H, Edmonton AB, Vajsar J, Paula F de, Zatz M. Calpainopathy: focus on a pediatric population. Journal of Child Neurology. 2003 ; 18( 3): 212.[citado 2024 nov. 14 ]
Vancouver
Kolski H, Edmonton AB, Vajsar J, Paula F de, Zatz M. Calpainopathy: focus on a pediatric population. Journal of Child Neurology. 2003 ; 18( 3): 212.[citado 2024 nov. 14 ]
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: 14 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. 14 ]
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. 14 ]
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: 14 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. 14 ]
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. 14 ]
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: 14 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. 14 ]
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. 14 ]
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: 14 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. 14 ]
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. 14 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 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. 14 ]
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. 14 ]

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