Congenital muscular dystrophy (CMD): a study of neuro-imaging findings in 25 merosin-deficient brazilian cases (2000)
- Authors:
- USP affiliated authors: MARIE, SUELY KAZUE NAGAHASHI - FM ; REED, UMBERTINA CONTI - FM ; DIAMENT, ARON JUDKA - FM ; SCAFF, MILBERTO - FM
- Unidade: FM
- Assunto: MÚSCULOS
- Language: Inglês
- Imprenta:
- Publisher place: South Africa
- Date published: 2000
- Source:
- Título do periódico: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 10, n. 4-5, p. 380, res. D.P.2.3, 2000
- Conference titles: International Congress of the World Muscle Society
-
ABNT
MARIE, Suely Kazue Nagahashi et al. Congenital muscular dystrophy (CMD): a study of neuro-imaging findings in 25 merosin-deficient brazilian cases. Neuromuscular Disorders. South Africa: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 15 maio 2024. , 2000 -
APA
Marie, S. K. N., Reed, U. C., Ferreira, L. G., Resende, M. B. D., Carvalho, M. S., Diament, A. J., & Scaff, M. (2000). Congenital muscular dystrophy (CMD): a study of neuro-imaging findings in 25 merosin-deficient brazilian cases. Neuromuscular Disorders. South Africa: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Marie SKN, Reed UC, Ferreira LG, Resende MBD, Carvalho MS, Diament AJ, Scaff M. Congenital muscular dystrophy (CMD): a study of neuro-imaging findings in 25 merosin-deficient brazilian cases. Neuromuscular Disorders. 2000 ; 10( 4-5): 380.[citado 2024 maio 15 ] -
Vancouver
Marie SKN, Reed UC, Ferreira LG, Resende MBD, Carvalho MS, Diament AJ, Scaff M. Congenital muscular dystrophy (CMD): a study of neuro-imaging findings in 25 merosin-deficient brazilian cases. Neuromuscular Disorders. 2000 ; 10( 4-5): 380.[citado 2024 maio 15 ] - Congenital muscular dystrophy (CMD): histopathological aspects in a Brazilian casuistic of 55 cases
- Congenital muscular dystrophy (CMD): clinical-immunochemical correlation in a Brazilian casuistic 40 cases
- Síndrome de Schwartz-Jampel: relato de 4 casos
- Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype
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- Deflazacort in Duchenne muscular dystrophy: preliminary results in a Brazilian series
- Hipotonia congênita de causa neuromuscular: revisão de 160 casos
- Importância da expressão das isoformas maturativas da miosina em miopatia por alteração mínimas
- Congenital myopathy with minimal changes: clinical and morphological aspects
- Schwartz-Jampel syndrome
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