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Brain & Development|January 26, 2005
Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphismStewart Macleod, Arup Mallik, John L Tolmie, et al.
Epilepsia|February 5, 2023
Comorbidities and predictors of health-related quality of life in Dravet syndrome: A 10-year, prospective follow-up studyPhoebe Makiello, Tony Feng, Benjamin Dunwoody, et al.
Epilepsia Open|December 9, 2021
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in EuropeElena Cardenal-Muñoz, Stéphane Auvin, Vicente Villanueva, et al.
Epilepsy & Behavior : E&B|April 22, 2017
The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future researchMark P Jensen, Andreas Brunklaus, Liam Dorris, et al.
Epilepsia|February 27, 2024
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsiesDeclan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Epilepsia|July 15, 2021
Time to onset of cannabidiol treatment effects in Dravet syndrome: Analysis from two randomized controlled trialsJennifer Madan Cohen, Daniel Checketts, Eduardo Dunayevich, et al.
Brain : a Journal of Neurology|October 23, 2021
Early childhood epilepsies: epidemiology, classification, aetiology, and socio-economic determinantsJoseph D Symonds, Katherine S Elliott, Jay Shetty, et al.
European Journal of Medical Genetics|May 26, 2022
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologistsAmy McTague, Andreas Brunklaus, Giulia Barcia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
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