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

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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Detalles Bibliográficos
Otros Autores: Tapia, Ricardo, author (author)
Formato: Libro electrónico
Idioma:Inglés
Publicado: France : Frontiers Media SA 2015
2015
Colección:Frontiers Research Topics,
Materias:
Neurology
Medicine
Health & Biological Sciences
trophic factors
motor neuron degeneration
skeletal
neuroinflammation
muscle
genetic expression
spinal cord
amyotrophic lateral sclerosis (ALS)
Ver en Biblioteca Universitat Ramon Llull:https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009428053706719

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