Investigating function and connectivity of morphometric findings — Exemplified on cerebellar atrophy in spinocerebellar ataxia 17 (SCA17)

Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disorder characterized by progressive cerebellar ataxia but also a broad spectrum of other neuropsychiatric signs. As anatomical and structural studies have shown severe cerebellar atrophy in SCA17 and a differenti...

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Udgivet i:Neuroimage
Main Authors: Reetz, Kathrin, Dogan, Imis, Rolfs, Arndt, Binkofski, Ferdinand, Schulz, Jörg B., Laird, Angela R., Fox, Peter T., Eickhoff, Simon B.
Format: Artigo
Sprog:Inglês
Udgivet: 2012
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4801477/
https://ncbi.nlm.nih.gov/pubmed/22659444
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroimage.2012.05.058
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