Multiple system atrophy: insights into a rare and debilitating movement disorder
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology
Link
http://www.nature.com/articles/nrneurol.2017.26.pdf
Reference152 articles.
1. Kollensperger, M. et al. Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry. Mov. Disord. 25, 2604–2612 (2010).
2. Lin, D. J., Hermann, K. L. & Schmahmann, J. D. The diagnosis and natural history of multiple system atrophy, cerebellar type. Cerebellum 15, 663–679 (2016).
3. Wenning, G. K. et al. The natural history of multiple system atrophy: a prospective European cohort study. Lancet Neurol. 12, 264–274 (2013). A large prospective, multicentre cohort study from Europe that describes the natural history of MSA and studies predictors for aggressive disease course.
4. Low, P. A. et al. Natural history of multiple system atrophy in the USA: a prospective cohort study. Lancet Neurol. 14, 710–719 (2015). A large prospective, multicentre cohort study from the USA that explores the natural history and determining predictors of accelerated decline in MSA.
5. Trojanowski, J. Q., Revesz, T. & Neuropathology Working Group on MSA. Proposed neuropathological criteria for the post mortem diagnosis of multiple system atrophy. Neuropathol. Appl. Neurobiol. 33, 615–620 (2007). Current neuropathological criteria to diagnose definite MSA.
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