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Persistent abnormalities in Rolandic thalamocortical white matter circuits in childhood epilepsy with centrotemporal spikes

OBJECTIVE: Childhood epilepsy with centrotemporal spikes (CECTS) is a common, focal, transient, developmental epilepsy syndrome characterized by unilateral or bilateral, independent epileptiform spikes in the Rolandic regions of unknown etiology. Given that CECTS presents during a period of dramatic...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Epilepsia
Hauptverfasser: Thorn, Emily L., Ostrowski, Lauren M., Chinappen, Dhinakaran M., Jing, Jin, Westover, M. Brandon, Stufflebeam, Steven M., Kramer, Mark A., Chu, Catherine J.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2020
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7722074/
https://ncbi.nlm.nih.gov/pubmed/32944938
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.16681
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