Articles with "sca2 patients" as a keyword



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Sleep spindles and K-complex activities are decreased in spinocerebellar ataxia type 2: relationship to memory and motor performances.

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Published in 2019 at "Sleep medicine"

DOI: 10.1016/j.sleep.2019.04.005

Abstract: BACKGROUND Sleep spindles and K-complexes are electroencephalographic hallmarks of non-rapid eye movement (non-REM) sleep that provide valuable information into brain functioning, plasticity and sleep functions in normal and pathological conditions. However, they have not been… read more here.

Keywords: sleep spindles; memory; relationship; spindles complexes ... See more keywords

“Mens Sana in Corpore Sano”: The Emerging Link of Motor Reserve with Motor and Cognitive Abilities and Compensatory Brain Networks in SCA2 Patients

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Published in 2022 at "Biomedicines"

DOI: 10.3390/biomedicines10092166

Abstract: The ability to resiliently cope with neuropathological lesions is a key scientific concern. Accordingly, this study aims to investigate whether motor reserve (MR), likely to be boosted by exercise engagement in a lifetime, affects motor… read more here.

Keywords: brain networks; motor; motor reserve; sca2 patients ... See more keywords
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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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Published in 2021 at "Neurology India"

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