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Sensitivity of brain MRI and neurological examination for detection of upper motor neurone degeneration in amyotrophic lateral sclerosis.

Abram D NitertHarold H G TanRenée WalhoutNienke L KnijnenburgMichael A van EsJan Herman VeldinkJeroen HendrikseHenk-Jan WestenengLeonard H van den Berg
Published in: Journal of neurology, neurosurgery, and psychiatry (2021)
Motor CT is a more sensitive measure of UMN degeneration than UMN signs. Motor CT and pyramidal tract FD are discriminative between patients and controls. Brain MRI can monitor UMN degeneration before signs become clinically evident. These findings promote MRI as a potential biomarker for UMN progression in clinical trials in ALS.
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