Article
Excitability properties of mouse motor axons in the mutant SOD1(G93A) model of amyotrophic lateral sclerosis.
Muscle & nerve - 1 Jun 2010
Boërio Delphine, Kalmar Bernadett, Greensmith Linda, Bostock Hugh
Abstract excerpt
Non-invasive excitability studies of motor axons in patients with amyotrophic lateral sclerosis (ALS) have revealed a changing pattern of abnormal membrane properties with disease progression, but the heterogeneity of the changes has made it difficult to relate them to pathophysiology. The SOD1(G...
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