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. 2013 Dec 12;5:82. doi: 10.3389/fnagi.2013.00082

Table 1.

Demographic and clinical characteristics of ALS and PLS patients [mean values (Standard Deviation)].

Diagnosis Age Gender Disease duration (months)* UMN score ALS∖FRS Bulbar score MRC total score Disease progression rate
ALS 57 (9) M:21-F:11 20.8 (19) 9 (5.8) 32.5 (3.6) 11.03 (1.4) 101.1 (13.6) 0.66 (0.75)
PLS 52 (11) M:1-F:9 45.9 (38) 14 (2.7) 33.5 (4.5) 10.5 (1.4) 117.5 (7.9) 0.18 (0.14)

M, males; F, females; UMN, upper motor neuron; ALS∖FRS, amyotrophic lateral sclerosis/functional rating scale; MRC, Medical Research Council scale. *Disease duration at the time of testing (a diagnosis of PLS was confirmed in participants with a disease duration <36 months at the time of testing).