The impact of upper and lower motor neuron burden on diagnostic certainty, and clinical course of spinal-onset amyotrophic lateral sclerosis: a cluster-based approach
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-023-11827-7.pdf
Reference32 articles.
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2. Brooks BR, Miller RG, Swash M et al (2000) El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Mot Neuron Disord 1:293–299. https://doi.org/10.1080/146608200300079536
3. Colombo E, Doretti A, Scheveger F et al (2023) Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis. J Neurol 270:511–518. https://doi.org/10.1007/s00415-022-11404-4
4. Zoccolella S, Introna A, Milella G et al (2021) Subclinical upper motor neuron involvement at the diagnosis may predict disease progression in a cohort of lower motor neuron syndromes from Southern Italy. J Neurol Sci 425:117392. https://doi.org/10.1016/j.jns.2021.117392
5. Zoccolella S, Mastronardi A, Scarafino A et al (2020) Motor-evoked potentials in amyotrophic lateral sclerosis: potential implications in detecting subclinical UMN involvement in lower motor neuron phenotype. J Neurol. https://doi.org/10.1007/s00415-020-10073-5
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1. Mapping lower-limbs muscle vulnerability in patients with ALS: The role of upper and lower motor neurons;Journal of the Neurological Sciences;2024-07
2. A Clinical Scale for Rating the Severity of Bulbar Lower Motor Neuron Dysfunction in Amyotrophic Lateral Sclerosis;Biomedicines;2023-07-20
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