Reproducibility, and sensitivity to motor unit loss in amyotrophic lateral sclerosis, of a novel MUNE method: MScanFit MUNE

Amyotrophic lateral sclerosis (ALS) is a fatal neuromuscular disease characterized by a decline in upper and lower motor neurons and a corresponding denervation of muscle fibers. This leads to progressive paralysis with a fatal outcome within an average of 3 years after diagnosis of the disease. (Couratier et al., 2016)

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