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. Author manuscript; available in PMC: 2014 Sep 1.
Published in final edited form as: Amyotroph Lateral Scler Frontotemporal Degener. 2013 May 2;14(0):463–469. doi: 10.3109/21678421.2013.787630

Table 1.

Baseline characteristics of ALS cohort

Cohort (N) Male/Female (N)(%) (N=342) Age at Onset (y)(CI) (N=312) Bulbar Site of Onset (N)(%) (N=313) Duration (y)(CI) (N=312) FH Motor Neuron Disease (N)(%)(N=313) FH Neuro-degeneration (N)(%)(N=313) Neuropathology (N)(%) (N=342) TDP-43 Type (1/2/3)(%) (N=30) Known Mutations (N)(%)
342 176/166 (51/49) 58.8 (57.6–60.0) 74/239 (24/76) 3.4 (3.1–3.8) 37/276 (12/88) 157/156 (50/50) 52/290 (15/85) 0/0/30 (0/0/100) 36 (11%)

Abbreviations: ALS = amyotrophic lateral sclerosis, N = number, y = years, CI = 95% confidence interval, and FH is family history. To estimate disease duration, intervals between age at onset and age at death or between age at onset and current age were calculated.

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