Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Epilepsy Research|March 23, 2013
TBC1D24 mutation associated with focal epilepsy, cognitive impairment and a distinctive cerebro-cerebellar malformationZaid Afawi, Simone Mandelstam, Amos D Korczyn, et al.
Brain Communications|February 19, 2021
Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencingChloe A Stutterd, Stefanie Brock, Katrien Stouffs, et al.
American Journal of Medical Genetics. Part A|March 10, 2023
A cryptic pathogenic NDUFV1 variant identified by RNA-seq in a patient with normal complex I activity in muscle and transient magnetic resonance imaging changesSharmila Kiss, John Christodoulou, David R Thorburn, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Clinical seizure manifestations in the absence of synaptic connectionsEmma Macdonald-Laurs, Catherine A Bailey, Sarah Barton, et al.
Journal of Paediatrics and Child Health|April 25, 2020
Neuronal ceroid lipofuscinosis type 2: an Australian case seriesAlexandra M Johnson, Simone Mandelstam, Ian Andrews, et al.
Epilepsia Open|October 30, 2021
Infantile-onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotypeGuillem de Valles-Ibáñez, Michael S Hildebrand, Melanie Bahlo, 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.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 12, 2019
EML1-associated brain overgrowth syndrome with ribbon-like heterotopiaRenske Oegema, George McGillivray, Richard Leventer, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|October 5, 2018
Australian Clinical Consensus Guideline: The diagnosis and acute management of childhood strokeTanya L Medley, Christina Miteff, Ian Andrews, et al.
Pageof 4