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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 7, 2024
Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire studyErin Freeman-Jones, Galia Wilson, Claire Eldred, et al.Journal of Neuropathology and Experimental Neurology|November 7, 2007
An investigation of the expression of G1-phase cell cycle proteins in focal cortical dysplasia type IIBMaria Thom, Lillian Martinian, Arjune Sen, et al.BMJ Open|May 7, 2026
Accuracy of epilepsy screening tools in community and primary care settings across countries in Sub-Saharan Africa: systematic review and meta-analysis protocolEmmanuel Kwame Darkwa, J Helen Cross, Patrick Adjei, et al.Seizure|June 24, 2017
Current practice and recommendations in UK epilepsy monitoring units. Report of a national survey and workshopKhalid Hamandi, Sandor Beniczky, Beate Diehl, et al.BMJ Neurology Open|January 12, 2022
Vagus nerve stimulation therapy in people with drug-resistant epilepsy (CORE-VNS): rationale and design of a real-world post-market comprehensive outcomes registryArjune Sen, Ryan Verner, James P Valeriano, et al.Epilepsy & Behavior : E&B|March 25, 2022
The clinical, economic, and humanistic burden of Dravet syndrome - A systematic literature reviewJoseph Sullivan, Alison M Deighton, Maria Candida Vila, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 11, 2024
Optogenetic Determination of Dynamic and Cell-Type-Specific Inhibitory Reversal PotentialsRichard J Burman, Tara Diviney, Alexandru Călin, et al.Brain & Development|January 26, 2005
The movement disorders of Coffin-Lowry syndromeJohn B P Stephenson, Mary C Hoffman, Aline J C Russell, et al.Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.Journal of Medical Genetics|July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal originSarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.Pageof 22