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Autor:
Mary Kay Floeter, Rachel F Smallwood Shoukry, Mike Clark, Caleb J Huang, Laura E. Danielian, Devin Bageac
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19:562-569
OBJECTIVE: The clinical diagnosis of primary lateral sclerosis can only be made after upper motor neuron symptoms have progressed for several years without developing lower motor neuron signs. The goal of the study was to identify neuroimaging change