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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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| Publicado no: | J Physiol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | 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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