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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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Autores principales: Verstraete, Esther, Veldink, Jan H., Mandl, Rene C. W., van den Berg, Leonard H., van den Heuvel, Martijn P.
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2011
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3166305/
https://ncbi.nlm.nih.gov/pubmed/21912680
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0024239
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