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Epilepsia|May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcomeBronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.Brain : a Journal of Neurology|March 10, 2007
The spectrum of SCN1A-related infantile epileptic encephalopathiesLouise A Harkin, Jacinta M McMahon, Xenia Iona, et al.Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.Journal of Neurology|October 19, 2014
Long-term outcome of epilepsy in patients with Prader-Willi syndromeAlberto Verrotti, Raffaella Cusmai, Daniela Laino, et al.Annals of Neurology|August 19, 2023
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic ArchitectureRebekah V Harris, Karen L Oliver, Piero Perucca, et al.Epilepsia|January 7, 2021
Expanding the phenotype of PIGS-associated early onset epileptic developmental encephalopathyStephanie Efthymiou, Marina Dutra-Clarke, Reza Maroofian, et al.Seizure|January 10, 2013
Lacosamide in pediatric and adult patients: comparison of efficacy and safetyAlberto Verrotti, Giulia Loiacono, Antonella Pizzolorusso, et al.Journal of Neurology|June 14, 2024
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in ItalyGiovanni Battista Dell'Isola, Antonella Fattorusso, Francesco Pisani, et al.American Journal of Human Genetics|June 6, 2015
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsyEmanuela Dazzo, Manuela Fanciulli, Elena Serioli, et al.Neuroscience Letters|March 22, 2008
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsyGiorgia Bovo, Erica Diani, Francesca Bisulli, et al.Pageof 77