research data . Dataset . 2015

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Open Access
  • Published: 03 Dec 2015
Abstract
<p>ALS, amyotrophic lateral sclerosis; ALSFRS-R, revised ALS functional rating scale; ALSSS, ALS severity scale;ALS-NC, ALS with normal cognition; ALS-ECI, ALS with executive cognitive impairment; ALS-FTLD, ALS with frontotemporal lobe degeneration; the disease progression rate was calculated according to the formula of (48-ALSFRS-R score)/disease duration(months).</p><p>Data were means±SD.</p><p>Demographic and clinical characteristics of ALS-NC, ALS-ECI and ALS-FTLD.</p>
Subjects
free text keywords: Uncategorised, frontotemporal lobe degeneration, Chinese patients, 76 age, executive area, Chinese ALS patients, Neuropsychological performances, Sporadic Amyotrophic Lateral Sclerosis BackgroundIt, visuospatial function, NECI, neuropsychological tests, executive dysfunction, 106 incident patients, comorbid FTLD, Cognitive Dysfunction, eci, severer bulbar function, executive function, comparison.Results 106 patients, ALS cases, cognitive impairment, age distribution
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Dataset . 2015
Provider: figshare
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