Matthew Harms, MD
Assistant Professor of Neurology
Genetic causes of hereditary neuromuscular diseases Read More
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Genetic causes of hereditary neuromuscular diseases
Dr. Harms’ research focuses on uncovering the genetic causes of hereditary neuromuscular diseases. His clinical activities focus on the evaluation and treatment of patients with neuromuscular disease, including neuropathy, myopathy, myasthenia gravis, and amyotrophic lateral sclerosis. Dr. Harms also participates as an investigator for clinical trials in these diseases, and performs electromyography/nerve conduction studies.