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Trabalho de evento-resumo periodico
Congenital muscular dystrophy (CMD): histopathological aspects in a Brazilian casuistic of 55 cases (2000)
Ferreira, L.G.; Reed, Umbertina Conti; Resende, M.B.D.; Reed, Umbertina Conti; Carvalho, M.S.; Diament, Aron Judka; Scaff, Milberto; Marie, Suely Kazue Nagahashi
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, L.G. et al. Congenital muscular dystrophy (CMD): histopathological aspects in a Brazilian casuistic of 55 cases. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2000
APA
Ferreira, L. G., Reed, U. C., Resende, M. B. D., Reed, U. C., Carvalho, M. S., Diament, A. J., et al. (2000). Congenital muscular dystrophy (CMD): histopathological aspects in a Brazilian casuistic of 55 cases. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Ferreira LG, Reed UC, Resende MBD, Reed UC, Carvalho MS, Diament AJ, Scaff M, Marie SKN. Congenital muscular dystrophy (CMD): histopathological aspects in a Brazilian casuistic of 55 cases. Neuromuscular Disorders. 2000 ; 10( 4-5): 380.[citado 2024 nov. 11 ]
Vancouver
Ferreira LG, Reed UC, Resende MBD, Reed UC, Carvalho MS, Diament AJ, Scaff M, Marie SKN. Congenital muscular dystrophy (CMD): histopathological aspects in a Brazilian casuistic of 55 cases. Neuromuscular Disorders. 2000 ; 10( 4-5): 380.[citado 2024 nov. 11 ]
Trabalho de evento-resumo periodico
Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype (2000)
Reed, Umbertina Conti; Ferreira, L.G.; Resende, M.B.D.; Carvalho, M.S.; Diament, Aron Judka; Scaff, Milberto; Marie, Suely Kazue Nagahashi
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2000
APA
Reed, U. C., Ferreira, L. G., Resende, M. B. D., Carvalho, M. S., Diament, A. J., Scaff, M., & Marie, S. K. N. (2000). Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Ferreira LG, Resende MBD, Carvalho MS, Diament AJ, Scaff M, Marie SKN. Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype. Neuromuscular Disorders. 2000 ; 10( 4-5): 380.[citado 2024 nov. 11 ]
Vancouver
Reed UC, Ferreira LG, Resende MBD, Carvalho MS, Diament AJ, Scaff M, Marie SKN. Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype. Neuromuscular Disorders. 2000 ; 10( 4-5): 380.[citado 2024 nov. 11 ]
Trabalho de evento-resumo periodico
MHC class 1 as an additional marker to the course of juvenille dermatomyositis (2000)
Sallum, A.M.E.; Yoko, M.; Resende, M.B.D.; Ferreira, L.G.; Reed, Umbertina Conti; Carvalho, M.S.; Sacchetti, S.B.; Silva, C.A.A.; Kiss, M. H. B.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALLUM, A.M.E. et al. MHC class 1 as an additional marker to the course of juvenille dermatomyositis. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2000
APA
Sallum, A. M. E., Yoko, M., Resende, M. B. D., Ferreira, L. G., Reed, U. C., Carvalho, M. S., et al. (2000). MHC class 1 as an additional marker to the course of juvenille dermatomyositis. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Sallum AME, Yoko M, Resende MBD, Ferreira LG, Reed UC, Carvalho MS, Sacchetti SB, Silva CAA, Kiss MHB. MHC class 1 as an additional marker to the course of juvenille dermatomyositis. Neuromuscular Disorders. 2000 ; 10( 4-5): 358.[citado 2024 nov. 11 ]
Vancouver
Sallum AME, Yoko M, Resende MBD, Ferreira LG, Reed UC, Carvalho MS, Sacchetti SB, Silva CAA, Kiss MHB. MHC class 1 as an additional marker to the course of juvenille dermatomyositis. Neuromuscular Disorders. 2000 ; 10( 4-5): 358.[citado 2024 nov. 11 ]
Trabalho de evento-resumo periodico
Merosin-positive congenital muscular dystrophy(CMD): reporte of a case with marked reduction of "Beta"1 laminin chain immunoreactivity (2000)
Reed, Umbertina Conti; Ferreira, L.G.; Resende, M.B.D.; Carvalho, M.S.; Diament, Aron Judka; Scaff, Milberto; Marie, Suely Kazue Nagahashi
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Merosin-positive congenital muscular dystrophy(CMD): reporte of a case with marked reduction of "Beta"1 laminin chain immunoreactivity. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2000
APA
Reed, U. C., Ferreira, L. G., Resende, M. B. D., Carvalho, M. S., Diament, A. J., Scaff, M., & Marie, S. K. N. (2000). Merosin-positive congenital muscular dystrophy(CMD): reporte of a case with marked reduction of "Beta"1 laminin chain immunoreactivity. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Ferreira LG, Resende MBD, Carvalho MS, Diament AJ, Scaff M, Marie SKN. Merosin-positive congenital muscular dystrophy(CMD): reporte of a case with marked reduction of "Beta"1 laminin chain immunoreactivity. Neuromuscular Disorders. 2000 ; 10( 4-5): 381.[citado 2024 nov. 11 ]
Vancouver
Reed UC, Ferreira LG, Resende MBD, Carvalho MS, Diament AJ, Scaff M, Marie SKN. Merosin-positive congenital muscular dystrophy(CMD): reporte of a case with marked reduction of "Beta"1 laminin chain immunoreactivity. Neuromuscular Disorders. 2000 ; 10( 4-5): 381.[citado 2024 nov. 11 ]
Trabalho de evento-resumo periodico
Congenital muscular dystrophy (CMD): clinical-immunochemical correlation in a Brazilian casuistic 40 cases (2000)
Reed, Umbertina Conti; Vainzof, Mariz ; Resende, M.B.D.; Carvalho, M.S.; Diament, Aron Judka; Scaff, Milberto; Marie, Suely Kazue Nagahashi; Resende, M.B.D.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Congenital muscular dystrophy (CMD): clinical-immunochemical correlation in a Brazilian casuistic 40 cases. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2000
APA
Reed, U. C., Vainzof, M., Resende, M. B. D., Carvalho, M. S., Diament, A. J., Scaff, M., et al. (2000). Congenital muscular dystrophy (CMD): clinical-immunochemical correlation in a Brazilian casuistic 40 cases. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Vainzof M, Resende MBD, Carvalho MS, Diament AJ, Scaff M, Marie SKN, Resende MBD. Congenital muscular dystrophy (CMD): clinical-immunochemical correlation in a Brazilian casuistic 40 cases. Neuromuscular Disorders. 2000 ; 10( 4-5): 381.[citado 2024 nov. 11 ]
Vancouver
Reed UC, Vainzof M, Resende MBD, Carvalho MS, Diament AJ, Scaff M, Marie SKN, Resende MBD. Congenital muscular dystrophy (CMD): clinical-immunochemical correlation in a Brazilian casuistic 40 cases. Neuromuscular Disorders. 2000 ; 10( 4-5): 381.[citado 2024 nov. 11 ]

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