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American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.Epilepsia Open|September 11, 2020
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study groupJoerg Klepper, Cigdem Akman, Marisa Armeno, et al.Epilepsy Research|August 21, 2024
Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?Paula Marques, Patrick B Moloney, Caihong Ji, et al.Physiological Measurement|May 21, 2024
Multimodal wearable EEG, EMG and accelerometry measurements improve the accuracy of tonic-clonic seizure detectionJingwei Zhang, Lauren Swinnen, Christos Chatzichristos, et al.Neurology|July 22, 2020
Neuronal antibody prevalence in children with seizures under 3 years: A prospective national cohortJoseph D Symonds, Teresa C Moloney, Bethan Lang, et al.JMIR Neurotechnology|December 4, 2025
Clinical Perspectives on Using Remote Measurement Technology in Assessing Epilepsy, Multiple Sclerosis, and Depression: Delphi StudyJacob A Andrews, Michael P Craven, Boliang Guo, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 20, 2025
Is resective surgery cost-effective for adults with epilepsy? A cost-utility analysis in a publicly funded healthcare systemAlexandra Bonnon, Paul Kopanidis, Sophia Kemmis-Betty, et al.Brain : a Journal of Neurology|July 15, 2019
Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohortJoseph D Symonds, Sameer M Zuberi, Kirsty Stewart, et al.Epilepsy & Behavior : E&B|September 4, 2021
Impact of the COVID-19 pandemic on people with epilepsy: Findings from the Brazilian arm of the COV-E studyMaria Andraus, Jennifer Thorpe, Xin You Tai, et al.Human Molecular Genetics|October 11, 2017
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disabilityBenjamin Davies, Laurence A Brown, Ondrej Cais, et al.Pageof 22