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Developmental Medicine and Child Neurology|June 10, 2021
Severe speech impairment is a distinguishing feature of FOXP1-related disorderRuth O Braden, David J Amor, Simon E Fisher, et al.Epilepsia|May 12, 2018
A population-based cost-effectiveness study of early genetic testing in severe epilepsies of infancyKatherine B Howell, Stefanie Eggers, Kim Dalziel, et al.Journal of Biomechanical Engineering|April 8, 2010
Hydrostatic pressure stimulation of human mesenchymal stem cells seeded on collagen-based artificial extracellular matricesRicarda Hess, Timothy Douglas, Kenneth A Myers, et al.Journal of Child Neurology|October 3, 2022
Surgically Remediable Secondary Network Epileptic Encephalopathies With Continuous Spike Wave in Sleep: Lesions May Not Be Visible on Brain Magnetic Resonance Imaging (MRI)Abdulla Alawadhi, Juan Pablo Appendino, Walter Hader, et al.Mitochondrion|February 12, 2026
Short telomeres in mitochondrial DNA depletion disordersYumi Dille, Emmanouil Rampakakis, Geraldine Aubert, et al.Epilepsia|April 17, 2013
SCN1A testing for epilepsy: application in clinical practiceShinichi Hirose, Ingrid E Scheffer, Carla Marini, et al.Journal of Paediatrics and Child Health|September 23, 2020
Protocol for a single patient therapy plan: A randomised, double-blind, placebo-controlled N-of-1 trial to assess the efficacy of cannabidiol in patients with intractable epilepsyKatherine S Ong, John B Carlin, Michael Fahey, et al.Epilepsia|March 10, 2017
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and TerminologyRobert S Fisher, J Helen Cross, Jacqueline A French, et al.Neurology|February 13, 2015
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizuresRhys H Thomas, Lin Mei Zhang, Gemma L Carvill, et al.Epilepsy Research|October 8, 2021
Dravet syndrome: A quick transition guide for the adult neurologistDanielle M Andrade, Anne T Berg, Veronica Hood, et al.Pageof 67