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Neurology|August 30, 2019
Efficacy and tolerability of adjunctive lacosamide in pediatric patients with focal seizuresViktor Farkas, Barbara Steinborn, J Robert Flamini, et al.Epilepsia|January 7, 2012
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikesDanya F Vears, Meng-Han Tsai, Lynette G Sadleir, et al.Frontiers in Neurology|April 1, 2022
Impaired Color Recognition in HCN1 Epilepsy: A Single Case ReportChaseley E Mckenzie, Chen-Jui Ho, Ian C Forster, et al.Journal of Neurology|January 23, 2024
Utility of genetic testing in the pre-surgical evaluation of children with drug-resistant epilepsySarah Alsubhi, Saoussen Berrahmoune, Roy W R Dudley, et al.The Journal of Cell Biology|July 9, 2014
Rac1 and Aurora A regulate MCAK to polarize microtubule growth in migrating endothelial cellsAlexander Braun, Kyvan Dang, Felinah Buslig, et al.Pediatric Neurology|January 15, 2026
Biallelic Rare COL18A1 Variants in Patients With Neurological Phenotypes Without Severe Ophthalmologic AbnormalitiesGuido Guberman, Marcello Scala, Pasquale Striano, et al.Epilepsia|July 6, 2019
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disabilityFelippe Borlot, Bruno Ivo de Almeida, Shari L Combe, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.NAR Genomics and Bioinformatics|April 7, 2025
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array dataErandee Robertson, Bronwyn E Grinton, Karen L Oliver, et al.Pageof 67