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Handbook of Clinical Neurology|April 30, 2013
Genetics of idiopathic epilepsiesRima Nabbout, Ingrid E Scheffer
The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
Epilepsia|November 18, 2020
Transcriptome analysis of a ring chromosome 20 patient cohortKenneth A Myers, Mark F Bennett, Michael S Hildebrand, et al.
Brain : a Journal of Neurology|April 22, 2014
Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scn1b-based model of Dravet syndromeChristopher A Reid, Bryan Leaw, Kay L Richards, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.
NAR Genomics and Bioinformatics|April 7, 2025
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array dataErandee Robertson, Bronwyn E Grinton, Karen L Oliver, et al.
Autonomic Neuroscience : Basic & Clinical|May 6, 2014
Genetics of vasovagal syncopeKarl Martin Klein, Samuel F Berkovic
Neurology|November 15, 2006
What happens now? Ongoing outcome after post-temporal lobectomy seizure recurrenceAnne M McIntosh, Samuel F Berkovic
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