Monitoring respiratory muscle strength assists in early diagnosis of respiratory dysfunction as opposed to the isolated use of pulmonary function evaluation in amyotrophic lateral sclerosis
Objective: It was study the relationship between respiratory muscle strength and forced vital capacity (FVC) in patients with amyotrophic lateral sclerosis (ALS) versus healthy subjects. Methods: Pulmonary function and respiratory muscle strength [maximal inspiratory (PImax), maximal expiratory (PEm...
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Principais autores: | , , , , , |
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Formato: | article |
Idioma: | English |
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Arquivos de Neuro-Psiquiatria
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Endereço do item: | https://repositorio.ufrn.br/handle/123456789/54257 https://doi.org/10.1590/S0004-282X2013000300004 |
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