Differential involvement of corticospinal tract (CST) fibers in UMN-predominant ALS patients with or without CST hyperintensity: A diffusion tensor tractography study

Diagnosis of amyotrophic lateral sclerosis (ALS) depends on clinical evidence of combined upper motor neuron (UMN) and lower motor neuron (LMN) degeneration, although ALS patients can present with features predominantly of one or the other. Some UMN-predominant patients show hyperintense signal alon...

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Detalles Bibliográficos
Autores principales: Rajagopalan, Venkateswaran, Pioro, Erik P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349615/
https://www.ncbi.nlm.nih.gov/pubmed/28337412
http://dx.doi.org/10.1016/j.nicl.2017.02.017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349615/
https://www.ncbi.nlm.nih.gov/pubmed/28337412
http://dx.doi.org/10.1016/j.nicl.2017.02.017

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