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Frontiers in Neurology|August 30, 2023
Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohortYoung Jun Ko, Soo Yeon Kim, Seungbok Lee, et al.
Brain & Development|August 11, 2014
Clinical and mutational spectrum in Korean patients with Rubinstein-Taybi syndrome: the spectrum of brain MRI abnormalitiesJin Sook Lee, Christine K Byun, Hunmin Kim, et al.
Brain & Development|December 10, 2019
Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS)Ji Yeon Han, Sun Ah Choi, Yoon Gi Chung, et al.
Clinical and Experimental Pediatrics|February 19, 2026
Long-term outcome in children with infantile epileptic spasms syndrome: a multicenter retrospective study in KoreaSun Ah Choi, Minhye Kim, Hye Jin Kim, et al.
Journal of Epilepsy Research|January 28, 2022
The Role of Focal Epilepsy Features in Defining <i>SCN1A</i> Mutation-positive Dravet Syndrome as Generalized and Focal EpilepsyYoung Jun Ko, Il Han Yoo, Jiwon Lee, et al.
Journal of Epilepsy Research|January 28, 2015
Screening Autoimmune Anti-neuronal Antibodies in Pediatric Patients with Suspected Autoimmune EncephalitisSoo Yeon Kim, Sun Ah Choi, Hye Won Ryu, et al.
Brain & Development|April 20, 2021
Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signsWooJoong Kim, Jae So Cho, Young Kyu Shim, et al.
Epilepsy Research|January 3, 2017
FARS2 mutation and epilepsy: Possible link with early-onset epileptic encephalopathyJae So Cho, Seung Hyo Kim, Ha Young Kim, et al.
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