Glial Cells—The Strategic Targets in Amyotrophic Lateral Sclerosis Treatment

Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease, which is characterized by the degeneration of motor neurons in the motor cortex and the spinal cord and subsequently by muscle atrophy. To date, numerous gene mutations have been linked to both sporadic and familial ALS, but the ef...

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Detalles Bibliográficos
Autores principales: Filipi, Tereza, Hermanova, Zuzana, Tureckova, Jana, Vanatko, Ondrej, Anderova, Miroslava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020059/
https://www.ncbi.nlm.nih.gov/pubmed/31963681
http://dx.doi.org/10.3390/jcm9010261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020059/
https://www.ncbi.nlm.nih.gov/pubmed/31963681
http://dx.doi.org/10.3390/jcm9010261

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