Severity and functional ability scale for amyotrophic lateral sclerosis patients: preliminar results

Autores

  • Edmar Zanoteli Clínica de Doenças Neuromusculares da AACD (Associação de Assistência à Criança Deficiente)

DOI:

https://doi.org/10.4181/RNC.2008.16.194

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Referências

de Carvalho Silva LB, Mourão LF, Silva AA, Lima NM, Almeida SR, Franca MC Jr, et al. Amyotrophic lateral sclerosis: combined nutritional, respiratory and functional assessment. Arq Neuropsiquiatr 2008;66(2B):354-9.

Gordon PH, Cheung YK, Levin B, Andrews H, Doorish C, Macarthur RB, et al. A novel, efficient, randomized selection trial comparing combinations of drug therapy for ALS. Amyotroph Lateral Scler 2008;9(4):212-22.

Gordon PH, Miller RG, Moore DH. ALSFRS-R. Amyotroph Lateral Scler Other Motor Neuron Disord 2004;5(Suppl 1):90-3.

Kaufmann P, Levy G, Thompson JL, Delbene ML, Battista V, Gordon PH, et al. The ALSFRS predicts survival time in an ALS clinic population. Neurology 2005;64:38-43.

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Publicado

2008-09-30

Como Citar

Zanoteli, E. (2008). Severity and functional ability scale for amyotrophic lateral sclerosis patients: preliminar results. Revista Neurociências, 16(3), 174. https://doi.org/10.4181/RNC.2008.16.194

Edição

v. 16 n. 3 (2008)

Seção

Editorial
Recebido: 2019-03-05
Publicado: 2008-09-30

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