Sensory nerve conduction in amyotrophic lateral sclerosis

Abstract
Identification of median and ulnar sensory nerve potentials after electrical stimulation in patients with amyotrophic lateral sclerosis supports the clinical finding of normal sensory function in this disease. These action potentials are consistently found in the presence of severe muscular wasting. A single exception to this observation is cited in this review of 13 cases.

This publication has 4 references indexed in Scilit: