Doenças do neurônio motor

Autores

  • Marco Antonio Troccoli Chieia Escola Paulista de Medicina / Universidade Federal de São Paulo – UNIFESP.

DOI:

https://doi.org/10.34024/rnc.2005.v13.8803

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Referências

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Trainor BJ, Codd MB, Corr B, Forde C, Frost E, Hardiman OM. Clinical features of amiotrophic lateral sclerosis according to the El escorial and Arlie house diagnostic criteria: apopulation base study. Arch Neurol 2000;57;1171-6.

Andersen PM, Nilsson P, Keranen ML, et al. Phenotypic heterogeneity in motor neuron diseases patients with Cu/Zn- superoxido desmutase in Scandinavian. Brain 1997;120:1723-37.

Rosen DR, Sidique T, Patterson D, et al. Mutations Cu/Zn superoxide desmutase gene areassociated with familial lateral sclerosis. Nature 1993;362;59-62.

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Brahe C, Servidei S, Zappata S, et al. Genetic homogeneity between childhood-onset and adult onset autossomal recessive spinalmuscular atrophy. Lancet 1995; 346;741-42.

Brzustowicz LM, lehner T, Castilla LH, et al. Genetic mapping of chronic childhood onset spinal muscular atrophy to chromosome 5q11.2-q13.3. Nature 1990;344;540-541.

Zerres K, Rudnick S, Forkert R. Genetic basis of adult onset spinal muscular atrophy. Lancet 1995;346;1162.12. McComas AJ, Quartly C, Griggs RC. Early and late losses of motor units after poliomyelitis. Brain 1997;120:1415-1421.

Stalberg E, Grimby G. Dynamic eletromyographic and muscle biopsy changes in post-polio subjets. Muscle and Nerve 1995;18;699-707.

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Publicado

2005-09-30

Como Citar

1.
Chieia MAT. Doenças do neurônio motor. Rev Neurocienc [Internet]. 30º de setembro de 2005 [citado 9º de julho de 2025];13:26-30. Disponível em: https://periodicos.unifesp.br/index.php/neurociencias/article/view/8803