Structural cerebellar correlates of cognitive functions in spinocerebellar ataxia type 2
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DOI: 10.1007/s00415-018-8738-6
Abstract: Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative disease involving the cerebellum and characterized by a typical motor syndrome. In addition, the presence of cognitive impairment is now widely acknowledged as a feature… read more here.
Keywords: ataxia type; spinocerebellar ataxia; structural cerebellar; sca2 ... See more keywords
The Two Faces of Pediatric SCA2
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DOI: 10.1111/ene.70314
Abstract: Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurological disease usually described in adults. Expanded CAG repeats in the ATXN2 gene can lead to pediatric onset. This study aims to describe the natural history… read more here.
Keywords: pediatric sca2; history; faces pediatric; two faces ... See more keywords
Cortical and Subcortical Brain Area Atrophy in SCA1 and SCA2 Patients in India: The Structural MRI Underpinnings and Correlative Insight Among the Atrophy and Disease Attributes
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DOI: 10.4103/0028-3886.329596
Abstract: Introduction: Genetically defined spinocerebellar ataxia (SCA) type 1 and 2 patients have differential clinical profile along with probable distinctive cortical and subcortical neurodegeneration. We compared the degree of brain atrophy in the two subtypes with… read more here.
Keywords: sca2 patients; sca1 sca2; sca2; atrophy ... See more keywords