A clinically applicable approach for detecting spontaneous action potential spikes in amyotrophic lateral sclerosis

Faezeh Jahanmiri-Nezhad1, Xiaoyan Li, Paul E Barkhaus

  • 1*Sensory Motor Performance Program, Rehabilitation Institute of Chicago, Illinois, U.S.A.; †Department of Bioengineering, University of Illinois, Chicago, Illinois, U.S.A.; ‡Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin, U.S.A.; §Department of Physical Medicine and Rehabilitation, Northwestern University, Chicago, Illinois, U.S.A.; and ‖Institute of Biomedical Engineering, University of Science and Technology of China, Hefei, China.

Summary

A new high-density surface electromyogram (EMG) method simplifies detecting spontaneous muscle activity in amyotrophic lateral sclerosis (ALS) patients. This technique offers a fast, user-friendly approach for potential clinical use in diagnosing neuromuscular diseases.

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