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spinocerebellar ataxias
Summary
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Curated Studies
Most Correlated Studies
OMIM - Ataxia
OMIM - Spinocerebellar Ataxias
OMIM - Galloway-Mowat syndrome
Neurons from iPSCs generated from dermal fibroblasts/PBMCs of spinocerebellar ataxia 2 and 3 patient
Mouse Phenotypes - Degenerative disease of the CNS
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Literature
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Disease progression of spinocerebellar ataxia types 1, 2, 3 and 6 before and after ataxia onset.
Intermuscular Coherence in Spinocerebellar Ataxias 3 and 6: a Preliminary Study.
Composite autonomic severity scoring in spinocerebellar ataxia type 1 and 2.
Dopa-responsive dystonia in spinocerebellar ataxia 6: A case report.
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian…
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Clinical Trials
Most Relevant Clinical Trials
Dalfampridine and Gait in Spinocerebellar Ataxias
Identification of Biomarkers in Spinocerebellar Ataxia 3
Study of CAD-1883 for Spinocerebellar Ataxia
Measuring Neurological Impairment and Functional Visual Assessment In Spinocerebellar Ataxias
Efficacy Of Oral Trehalose In Spinocerebellar Ataxia 3
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