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Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.
Epilepsia|March 13, 2020
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsyLynette G Sadleir, Guillem de Valles-Ibáñez, Chontelle King, et al.
Annals of Neurology|July 7, 2017
Familial mesial temporal lobe epilepsy and the borderland of déjà vuPiero Perucca, Douglas E Crompton, Susannah T Bellows, et al.
Epilepsia Open|December 23, 2023
Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort studyRussell Nightscales, Zhibin Chen, Sarah Barnard, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
Developmental Medicine and Child Neurology|December 24, 2019
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizuresIngrid E Scheffer, Katja E Boysen, Amy L Schneider, et al.
Epilepsia|September 24, 2025
Atenolol rescues premature mortality in genetic mouse models of sudden unexpected death in epilepsyMing S Soh, Amanda Hu, Alibek Kuanyshbek, et al.
Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
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