Clinical and neurophysiological evaluation of progression in amyotrophic lateral sclerosis
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference14 articles.
1. Linear estimates of rates of disease progression as predictors of survival in patients with ALS entering clinical trials
2. Motor unit number estimates and quantitative muscle strength measurements of distal muscles in patients with amyotrophic lateral sclerosis
3. Linear estimates of disease progression predict survival in patients with amyotrophic lateral sclerosis
4. Motor unit number estimation, isometric strength, and electromyographic measures in amyotrophic lateral sclerosis
5. Electrophysiologic endpoint measures in a multicenter ALS drug trial
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3. Neurophysiological indices in amyotrophic lateral sclerosis correlate with functional outcome measures, staging and disease progression;Clinical Neurophysiology;2021-07
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5. Repeater F-waves in amyotrophic lateral sclerosis: Electrophysiologic indicators of upper or lower motor neuron involvement?;Clinical Neurophysiology;2020-01
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