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Publikováno v:
Frontiers in Cellular Neuroscience, Vol 8 (2014)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease manifested by progressive muscle atrophy and paralysis due to the loss of upper and lower motoneurons (MN). Spasticity appears in ALS patients leading to further disabling consequence
Externí odkaz:
https://doaj.org/article/80c7ec343a534549ae4c4044b4674518
