Showing results (161-170 of 731) with videos related to
Sort By:
Pageof 74
Human Molecular Genetics|April 30, 2004
GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsiesLeanne M Dibbens, Hua-Jun Feng, Michaella C Richards, et al.Epilepsia|April 26, 2008
Gene expression analysis in absence epilepsy using a monozygotic twin designIngo Helbig, Nicholas A Matigian, Lata Vadlamudi, et al.Social Neuroscience|January 14, 2011
Mirror neuron system involvement in empathy: a critical look at the evidenceAmee D Baird, Ingrid E Scheffer, Sarah J WilsonNeuroscience and Biobehavioral Reviews|January 21, 2017
Features of the broader autism phenotype in people with epilepsy support shared mechanisms between epilepsy and autism spectrum disorderAnnie E Richard, Ingrid E Scheffer, Sarah J WilsonBrain & Development|February 21, 2018
Hemiconvulsion-hemiplegia-epilepsy evolving to contralateral hemi-Lennox-Gastaut-like phenotypeKenneth A Myers, Ingrid E Scheffer, John S ArcherBrain : a Journal of Neurology|April 21, 2010
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsRichard J Leventer, Anna Jansen, Daniela T Pilz, et al.Nature Genetics|October 23, 2012
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsySarah E Heron, Katherine R Smith, Melanie Bahlo, et al.Genetics in Medicine Open|December 13, 2024
Mosaic variants detectable in blood extend the clinicogenetic spectrum of GLI3-related hypothalamic hamartomaTimothy E Green, Mark F Bennett, Ilka Immisch, et al.Epilepsia|October 31, 2012
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiencyTodor Arsov, Saul A Mullen, John A Damiano, et al.Epilepsia|April 17, 2018
Can mutation-mediated effects occurring early in development cause long-term seizure susceptibility in genetic generalized epilepsies?Christopher Alan Reid, Ben Rollo, Steven Petrou, et al.Pageof 74