Spinocerebellar ataxia type 3 with dopamine-responsive dystonia: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference12 articles.
1. Machado disease: A hereditary ataxia in Portuguese emigrants to Massachusetts
2. The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3
3. Machado-Joseph disease: An autosomal dominant motor system degeneration
4. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease
5. Machado-Joseph Disease in a Sicilian-American Family
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1. Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia;Neurology Genetics;2024-06
2. Drug repurposing of dopaminergic drugs to inhibit ataxin-3 aggregation;Biomedicine & Pharmacotherapy;2023-09
3. Drug repurposing of dopaminergic drugs to inhibit Ataxin-3 aggregation;2022-12-02
4. Pharmacotherapy for the management of the symptoms of Machado-Joseph Disease;Expert Opinion on Pharmacotherapy;2022-10-13
5. Initially with pure parkinsonian phenotype of spinocerebellar ataxia type 3: A rare case report and literature review;2022-09-20
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