Longitudinal assessment of cortical motor function in amyotrophic lateral sclerosis.

Averaged SICI decline was also evident in patients with bulbar onset ALS, declining from 5.2%±4.8 [CI: 0.4,10.0] to 2.2%±4.9 [CI: −2.7,7.0] (β = 5.33, p = 0.15), however, this did not reach statistical significance (Fig. 2 ).

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