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Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.
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Familial amyotrophic lateral sclerosis 2 trials · 29 incl. sub-types Sub-types →
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Progressive muscular atrophy 11 trials Sub-types →