Merosin-positive congenital muscular dystrophy: a clinical immunohistochemical study of nine patients with severe phenotype (2000)
- Authors:
- Reed, Umbertina Conti
- Ferreira, L.G.
- Resende, M.B.D. - Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP)
- Carvalho, M.S. - Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP)
- Diament, Aron Judka
- Scaff, Milberto
- Marie, Suely Kazue Nagahashi
- USP affiliated authors: MARIE, SUELY KAZUE NAGAHASHI - FM ; REED, UMBERTINA CONTI - FM ; DIAMENT, ARON JUDKA - FM ; SCAFF, MILBERTO - FM
- Unidade: FM
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Kidlington Oxford
- Date published: 2000
- Source:
- Título do periódico: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 10, n. 4-5, p. 380, June 2000
- Conference titles: International Congress of the World Muscle Society
-
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: 20 abr. 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 abr. 20 ] -
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 abr. 20 ] - 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
- Congenital muscular dystrophy (CMD): a study of neuro-imaging findings in 25 merosin-deficient brazilian cases
- Merosin-positive congenital muscular dystrophy(CMD): reporte of a case with marked reduction of "Beta"1 laminin chain immunoreactivity
- Deflazacort in Duchenne muscular dystrophy: preliminary results in a Brazilian series
- Hipotonia congênita de causa neuromuscular: revisão de 160 casos
- Síndrome de Schwartz-Jampel: relato de 4 casos
- Importância da expressão das isoformas maturativas da miosina em miopatia por alteração mínimas
- Schwartz-Jampel syndrome
- Congenital myopathy with minimal changes: clinical and morphological aspects
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
