Machado-Joseph disease in New England: Clinical description and distinction from the olivopontocerebellar atrophies
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference18 articles.
1. Machado disease: A hereditary ataxia in Portuguese emigrants to Massachusetts
2. Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia
3. Autosomal dominant striatonigral degeneration: A clinical, pathologic, and biochemical study of a new genetic disorder
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5. Joseph disease in a non-Portuguese family
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3. Staying Strong Toolbox: Co-design of a physical activity and lifestyle program for Aboriginal families with Machado-Joseph disease in the Top End of Australia;PLOS ONE;2021-02-05
4. Development of an AAV-Based MicroRNA Gene Therapy to Treat Machado-Joseph Disease;Molecular Therapy - Methods & Clinical Development;2019-12
5. Profile of extrapyramidal manifestations in 85 patients with spinocerebellar ataxia type 1, 2 and 3;Journal of Clinical Neuroscience;2014-06
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