Cellular and molecular mechanisms of motor neuron death in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS), which was described since 1869 by Jean Martin Charcot, is a devastating neurodegenerative disease characterized by the selective and progressive loss of upper and lower motor neurons of the cerebral cortex, brainstem and the spinal cord. The cognitive process is...

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Autor principal:	Ricardo Tapia
Format:	Online
Idioma:	anglès
Publicat:	Frontiers Media SA 2021
Matèries:	RC321-571 Q1-390 trophic factors motor neuron degeneration skeletal neuroinflammation muscle genetic expression spinal cord amyotrophic lateral sclerosis (ALS) thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAN Neurosciences
Accés en línia:	17705
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