Clinical Rating Scales for Ataxia
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-24345-5_10
Reference126 articles.
1. Anheim M, et al. Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management. Neurogenetics. 2010;11:1–12. https://doi.org/10.1007/s10048-009-0196-y.
2. Ashizawa T, et al. Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study. Orphanet J Rare Dis. 2013;8:177. https://doi.org/10.1186/1750-1172-8-177.
3. Assadi M, et al. Validating an Ataxia Functional Composite Scale in spinocerebellar ataxia. J Neurol Sci. 2008;268:136–9. https://doi.org/10.1016/j.jns.2007.11.016.
4. Bolzan G, et al. Quality of life since pre-ataxic phases of spinocerebellar ataxia type 3/Machado-Joseph disease. Cerebellum. 2021;21:297. https://doi.org/10.1007/s12311-021-01299-8.
5. Bourcier D, et al. Documenting the psychometric properties of the scale for the assessment and rating of ataxia to advance trial readiness of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. J Neurol Sci. 2020;417:117050. https://doi.org/10.1016/j.jns.2020.117050.
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