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Research supported by Italian Ministry of Health. Project RF-2011-02347420 - Monitoring disease progression and phenotypic heterogeneity in hereditary ataxias: clinical, cognitive, neuroimaging, and neurophysiological study to identify early markers of cerebellar dysfunction in patients and presymptomatic carriers
Clinical database containing genetic test, neurological examination, cognitive tests, and brain MRI of 42 subjects: (14 SCA2 patients, 13 presymptomatic SCA2 subjects,5 gene-negative healthy controls)
cerebellar structural MRI, Cerebellar lobule segmentation, spinocerebellar ataxia (SCA2), cortical thickness, pre-symptomatic gene carriers, cognitive assessment, symbol digit modalities test
cerebellar structural MRI, Cerebellar lobule segmentation, spinocerebellar ataxia (SCA2), cortical thickness, pre-symptomatic gene carriers, cognitive assessment, symbol digit modalities test
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