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Brain Communications|June 2, 2023
Cation leak: a common functional defect causing HCN1 developmental and epileptic encephalopathyChaseley E McKenzie, Ian C Forster, Ming S Soh, et al.Expert Opinion on Therapeutic Targets|June 26, 2023
SCN1A as a therapeutic target for Dravet syndromeKenneth A MyersCMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|December 15, 2010
Holiday reading: Cigarette smoking: an underused tool in high-performance endurance trainingKenneth A MyersEpileptic Disorders : International Epilepsy Journal with Videotape|September 22, 2007
GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two childrenYu Hong Deng, Samuel F Berkovic, Ingrid E SchefferJournal of Sleep Research|February 27, 2018
A case series of lacosamide as adjunctive therapy in refractory sleep-related hypermotor epilepsy (previously nocturnal frontal lobe epilepsy)Shanika R Samarasekera, Samuel F Berkovic, Ingrid E SchefferCurrent Opinion in Neurology|March 14, 2007
Vaccination, seizures and 'vaccine damage'Natasha J Brown, Samuel F Berkovic, Ingrid E SchefferSocial Neuroscience|January 14, 2011
Mirror neuron system involvement in empathy: a critical look at the evidenceAmee D Baird, Ingrid E Scheffer, Sarah J WilsonNeuroscience and Biobehavioral Reviews|January 21, 2017
Features of the broader autism phenotype in people with epilepsy support shared mechanisms between epilepsy and autism spectrum disorderAnnie E Richard, Ingrid E Scheffer, Sarah J WilsonBrain & Development|July 27, 2002
Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARXPetter Strømme, Marie E Mangelsdorf, Ingrid E Scheffer, et al.Pageof 66