Article
Murine experimental models of amyotrophic lateral sclerosis: an update.
Neurologia - 1 Apr 2024
Moreno-Jiménez L, Benito-Martín M S, Sanclemente-Alamán I, Matías-Guiu J A, Sancho-Bielsa F, Canales-Aguirre A, Mateos-Díaz J C, Matías-Guiu J, Aguilar J, Gómez-Pinedo U
Abstract excerpt
INTRODUCTION: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease whose aetiology is unknown. It is characterised by upper and lower motor neuron degeneration. Approximately 90% of cases of ALS are sporadic, whereas the other 10% are familial. Regardless of whether the case is familial o sporadic, patients will develop progressive weakness, muscle atrophy with spasticity, and muscle...
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