Neuropsychological impairment in amyotrophic lateral sclerosis–frontotemporal spectrum disorder
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
https://www.nature.com/articles/s41582-023-00878-z.pdf
Reference139 articles.
1. Marin, B. et al. Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis. Int. J. Epidemiol. 46, 57–74 (2017).
2. Cronin, S., Hardiman, O. & Traynor, B. J. Ethnic variation in the incidence of ALS: a systematic review. Neurology 68, 1002–1007 (2007).
3. Sennfält, S. et al. The path to diagnosis in ALS: delay, referrals, alternate diagnoses, and clinical progression. Amyotroph. Lateral Scler. Frontotemporal Degener. 24, 45–53 (2023).
4. Strong, M. J. et al. Amyotrophic lateral sclerosis – frontotemporal spectrum disorder (ALS-FTSD): revised diagnostic criteria. Amyotroph. Lateral Scler. Frontotemporal Degener. 18, 153–174 (2017).
5. Beeldman, E. et al. The cognitive profile of ALS: a systematic review and meta-analysis update. J. Neurol. Neurosurg. Psychiatry 87, 611–619 (2016).
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3. Longevity of a Brain–Computer Interface for Amyotrophic Lateral Sclerosis;New England Journal of Medicine;2024-08-15
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