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. 2016 May 10;10:204. doi: 10.3389/fnins.2016.00204

Table 1.

Demographic Data of the participants.

Group ALSa Controls p valuec
Age (years) 49.05 ± 8.07529–71) 51.00 ± 10.576 (24–65) 0.386
Male: female 26:13 21:18 0.247
El Escorial criteria (probable/definite) 12/27
Disease duration (months) 17.77 ± 13.0012–71)
ALSFRS-Ra 36.18 ± 6.472 (16–44)
Disease progression rateb 0.9210 ± 0.70944 (0.17–3.14)
a

ALS, amyotrophic lateral sclerosis; ALSFRS_R, ALS Functional Rating Scale_Revised.

b

Disease progression rate = (48–ALSFRS_R)/Disease duration.

c

Statistical significance was set at p < 0.05.

HHS Vulnerability Disclosure