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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Verstraete, Esther, Veldink, Jan H., Mandl, Rene C. W., van den Berg, Leonard H., van den Heuvel, Martijn P.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2011
Pynciau:
Research Article
Mynediad Ar-lein: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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