The objective of this study was to examine the contribution of lower motor neuron (LMN) and upper motor neuron (UMN) dysfunction to weakness and impaired motor control in 27 patients with amyotrophic lateral sclerosis (ALS). Isometric strength was measured by dorsiflexor maximum voluntary contractio
Longitudinal study of functional spinal alpha motor neuron loss in amyotrophic lateral sclerosis
โ Scribed by K. Arasaki; Y. Kato; A. Hyodo; R. Ushijima; M. Tamaki
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 189 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
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