In vivo evidence for reduced ion channel expression in motor axons of patients with amyotrophic lateral sclerosis

KEY POINTS: The progressive loss of motor units in amyotrophic lateral sclerosis (ALS) is initially compensated for by the reinnervation of denervated muscle fibres by surviving motor axons. A disruption in protein homeostasis is thought to play a critical role in the pathogenesis of ALS. The change...

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Dettagli Bibliografici
Pubblicato in:J Physiol
Autori principali: Howells, James, Matamala, José Manuel, Park, Susanna B., Garg, Nidhi, Vucic, Steve, Bostock, Hugh, Burke, David, Kiernan, Matthew C.
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2018
Soggetti:
Neuroscience
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6235931/
https://ncbi.nlm.nih.gov/pubmed/30175403
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP276624
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