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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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Autori principali: Verstraete, Esther, Veldink, Jan H., Mandl, Rene C. W., van den Berg, Leonard H., van den Heuvel, Martijn P.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2011
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Accesso online: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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