Amyotrophic Lateral Sclerosis (Lou Gehrig Disease (cont.)
Medical Author:
Fernando Dangond, MD
Medical Editor:
Melissa Conrad Stöppler, MD, Chief Medical Editor
Melissa Conrad Stöppler, MD, Chief Medical EditorMelissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology. IN THIS ARTICLE
Synonyms and Keywordsamyotrophic lateral sclerosis, ALS, glutamate, Lou Gehrig's disease, Lou Gehrigs disease, symptoms of ALS, symptoms of amyotrophic lateral sclerosis, Lou Gehrig's disease symptoms, motor neuron disease, movement, muscle atrophy, nerve disorders, neurotransmitter, paralysis, paralyzed, respiratory failure, weakness, voluntary movement, neurons, nerve cells, SOD1 gene |
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Amyotrophic Lateral Sclerosis »
Amyotrophic lateral sclerosis (ALS) is a disease of unknown cause characterized by slowly progressive degeneration of upper motor neurons (UMNs) and lower motor neurons (LMNs).
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