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Frontiers in Neurology|October 5, 2020
Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?Lauren E Bleakley, Ming S Soh, Richard D Bagnall, et al.Epilepsy Research|June 20, 2015
Myoclonic occipital photosensitive epilepsy with dystonia (MOPED): A familial epilepsy syndromeLynette G Sadleir, Sarah Paterson, Katherine R Smith, et al.Brain Communications|January 8, 2024
Exploring individual fixel-based white matter abnormalities in epilepsyRemika Mito, Mangor Pedersen, Heath Pardoe, et al.Radiology|June 30, 2016
Periventricular Nodular Heterotopia: Detection of Abnormal Microanatomic Fiber Structures with Whole-Brain Diffusion MR Imaging TractographyShawna Farquharson, J-Donald Tournier, Fernando Calamante, et al.Cold Spring Harbor Molecular Case Studies|October 15, 2021
Identification of a recurrent mosaic KRAS variant in brain tissue from an individual with nevus sebaceous syndromeTimothy E Green, Duncan MacGregor, Susan M Carden, et al.Molecular and Cellular Neurosciences|May 1, 2007
A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channelRuwei Xu, Evan A Thomas, Misty Jenkins, et al.European Journal of Nuclear Medicine and Molecular Imaging|August 4, 2005
Assessment of the role of FDG PET in the diagnosis and management of children with refractory epilepsyGlenn P Ollenberger, Amanda J Byrne, Salvatore U Berlangieri, et al.Seizure|September 12, 2003
Risk factors for sudden unexpected death in epilepsy: a controlled prospective study based on coroners casesKenneth Opeskin, Samuel F BerkovicTrends in Molecular Medicine|July 11, 2006
Febrile seizures: traffic slows in the heatSamuel F Berkovic, Steven PetrouEpilepsy Research|November 12, 2013
Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutationsLynette G Sadleir, Dahbia Agher, Elodie Chabrol, et al.Pageof 73