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Annals of Neurology|May 4, 2010
Augmented currents of an HCN2 variant in patients with febrile seizure syndromesLeanne M Dibbens, Christopher A Reid, Bree Hodgson, 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|March 6, 2012
Febrile infection-related epilepsy syndrome is not caused by SCN1A mutationsDaniel Carranza Rojo, A Simon Harvey, Xenia Iona, et al.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.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.EMBO Reports|March 27, 2014
A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formationMartin Puskarjov, Patricia Seja, Sarah E Heron, et al.Neurology|August 10, 2014
Genetics of epilepsy: The testimony of twins in the molecular eraLata Vadlamudi, Roger L Milne, Kate Lawrence, et al.American Journal of Human Genetics|August 28, 2010
A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Mark A Corbett, Melanie Bahlo, Lachlan Jolly, et al.Neurology|April 17, 2013
Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26Karl Martin Klein, Catherine J Bromhead, Katherine R Smith, et al.Pageof 7