Impaired Structural Motor Connectome in Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disease selectively affecting upper and lower motor neurons. Patients with ALS suffer from progressive paralysis and eventually die on average after three years. The underlying neurobiology of upper motor neuron degeneration and its e...

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Detalles Bibliográficos
Autores principales: Verstraete, Esther, Veldink, Jan H., Mandl, Rene C. W., van den Berg, Leonard H., van den Heuvel, Martijn P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166305/
https://www.ncbi.nlm.nih.gov/pubmed/21912680
http://dx.doi.org/10.1371/journal.pone.0024239

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166305/
https://www.ncbi.nlm.nih.gov/pubmed/21912680
http://dx.doi.org/10.1371/journal.pone.0024239

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