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Epilepsia|February 8, 2023
Differential diagnosis of familial adult myoclonic epilepsyBetul Baykan, Silvana Franceschetti, Laura Canafoglia, et al.
Epilepsia|December 5, 2012
Family studies of individuals with eyelid myoclonia with absencesLynette G Sadleir, Danya Vears, Brigid Regan, et al.
Developmental Medicine and Child Neurology|February 12, 2023
Indications and prescribing patterns of antiseizure medications in children in New ZealandShayma Ali, James Stanley, Suzanne Davis, et al.
Neurology|February 7, 2023
Rates of Status Epilepticus and Sudden Unexplained Death in Epilepsy in People With Genetic Developmental and Epileptic EncephalopathiesAlice M Donnan, Amy L Schneider, Sophie Russ-Hall, 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.
Brain : a Journal of Neurology|June 18, 2004
Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?Isabella Taylor, Carla Marini, Michael R Johnson, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Channelopathies in idiopathic epilepsySarah E Heron, Ingrid E Scheffer, Samuel F Berkovic, et al.
Neurology|February 3, 2017
Dysarthria and broader motor speech deficits in Dravet syndromeSamantha J Turner, Amy Brown, Marta Arpone, et al.
Archives of Neurology|March 14, 2012
Progressive gait deterioration in adolescents with Dravet syndromeJill M Rodda, Ingrid E Scheffer, Jacinta M McMahon, et al.
Epilepsia|January 9, 2013
Siblings with refractory occipital epilepsy showing localized network activity on EEG-fMRIPatrick W Carney, A Simon Harvey, Samuel F Berkovic, et al.
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