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Article

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.

Cerebellum (London, England) - 1 Jun 2010

Reetz Kathrin, Lencer Rebekka, Hagenah Johannes M, Gaser Christian, Tadic Vera, Walter Uwe, Wolters Alexander, Steinlechner Susanne, Zühlke Christine, Brockmann Katja, Klein Christine, Rolfs Arndt, Binkofski Ferdinand

Abstract excerpt

Spinocerebellar ataxia (SCA17) is a rare genetic disorder characterized by a variety of neuropsychiatric symptoms. Recently, using magnetic resonance imaging (MRI) voxel-based morphometry (VBM), several specific functional-structural correlations comprising differential degeneration related to motor and psychiatric symptoms were reported in patients with SCA17. To investigate gray matter volume (GMV) changes over...

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PMID: 20016963
DOI: 10.1007/s12311-009-0150-4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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