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Epilepsia|December 5, 2008
Cognitive complaints after a first seizure in adulthood: Influence of psychological adjustmentSarah L Velissaris, Sarah J Wilson, Mark R Newton, et al.
Developmental Medicine and Child Neurology|November 8, 2017
Sleep problems in Dravet syndrome: a modifiable comorbidityShane H Licheni, Jacinta M Mcmahon, Amy L Schneider, et al.
Neurology|February 3, 2017
Dysarthria and broader motor speech deficits in Dravet syndromeSamantha J Turner, Amy Brown, Marta Arpone, et al.
Neurology. Genetics|May 5, 2018
Somatic GNAQ mutation in the forme fruste of Sturge-Weber syndromeMichael S Hildebrand, A Simon Harvey, Stephen Malone, et al.
Epilepsia|August 24, 2010
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyriaKate M Lawrence, Davide Mei, Mark R Newton, et al.
Epilepsia|April 23, 2004
Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex familiesCarla Marini, Ingrid E Scheffer, Kathryn M Crossland, et al.
Epilepsia|February 27, 2009
EEG features of absence seizures in idiopathic generalized epilepsy: impact of syndrome, age, and stateLynette Grant Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Epilepsy & Behavior : E&B|August 29, 2020
Cognitive, behavioral, and social functioning in children and adults with Dravet syndromeAmy Brown, Marta Arpone, Amy L Schneider, et al.
Epilepsia Open|July 4, 2024
Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox-Gastaut syndrome in clinical practiceElaine C Wirrell, Lieven Lagae, Ingrid E Scheffer, et al.
Epilepsia|February 27, 2025
Operational definition of developmental and epileptic encephalopathies to underpin the design of therapeutic trialsIngrid E Scheffer, Jacqueline French, Kette D Valente, et al.
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