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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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Detaylı Bibliyografya
Yayımlandı:Neuroimage Clin
Asıl Yazarlar: Rajagopalan, Venkateswaran, Pioro, Erik P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2017
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5349615/
https://ncbi.nlm.nih.gov/pubmed/28337412
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2017.02.017
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