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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.Brain : a Journal of Neurology|September 25, 2010
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritanceDouglas E Crompton, Ingrid E Scheffer, Isabella Taylor, et al.Proceedings of the National Academy of Sciences of the United States of America|November 27, 2024
Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathyMario Nappi, Giulio Alberini, Alessandro Berselli, et al.Epilepsia|April 17, 2015
Early and effective treatment of KCNQ2 encephalopathyTiziana Pisano, Adam L Numis, Sinéad B Heavin, et al.Neurocritical Care|September 23, 2008
The utility of conductive plastic electrodes in prolonged ICU EEG monitoringRohit R Das, Brendan P Lucey, Sherry H-Y Chou, et al.International Journal of Molecular Sciences|October 30, 2020
Tracing Autism Traits in Large Multiplex Families to Identify Endophenotypes of the Broader Autism PhenotypeKrysta J Trevis, Natasha J Brown, Cherie C Green, et al.Neuron|January 5, 2018
Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 EpilepsyDaniel T Pederick, Kay L Richards, Sandra G Piltz, et al.Annals of Neurology|May 4, 2010
Augmented currents of an HCN2 variant in patients with febrile seizure syndromesLeanne M Dibbens, Christopher A Reid, Bree Hodgson, et al.Pageof 57