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3. C09 SCAS genes as disease modifiers in huntington's disease. (September 2018)

4. Clinical and genetic characteristics of late-onset Huntington's disease. (April 2019)

5. Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction. (15th March 2018)

6. Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study. Issue 9 (September 2020)

7. F28 The contribution of attentional defects on motor, functional, and psychopathological dysfunctions in huntington's disease. (September 2018)