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Sensorimotor, Visual, and Auditory Cortical Atrophy in Unverricht-Lundborg Disease Mapped with Cortical Thickness Analysis

BACKGROUND AND PURPOSE: EPM1, caused by mutations in the CSTB gene, is the most common form of PME. The most incapacitating symptom of EPM1 is action-activated and stimulus-sensitive myoclonus. The clinical severity of the disease varies considerably among patients, but so far, no correlations have...

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Bibliografiske detaljer
Udgivet i:AJNR Am J Neuroradiol
Main Authors: Koskenkorva, P., Niskanen, E., Hyppönen, J., Könönen, M., Mervaala, E., Soininen, H., Kälviäinen, R., Vanninen, R.
Format: Artigo
Sprog:Inglês
Udgivet: American Society of Neuroradiology 2012
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7968823/
https://ncbi.nlm.nih.gov/pubmed/22268086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A2882
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