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The Lancet. Neurology|March 20, 2009
The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizuresDouglas E Crompton, Samuel F BerkovicNature Reviews. Neurology|April 16, 2014
The hidden genetics of epilepsy-a clinically important new paradigmRhys H Thomas, Samuel F BerkovicEpilepsia|March 19, 2009
Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?Angelique E J Sijben, Pasiri Sithinamsuwan, Ashalata Radhakrishnan, et al.Neurology|September 27, 2013
Copy number variants are frequent in genetic generalized epilepsy with intellectual disabilitySaul A Mullen, Gemma L Carvill, Susannah Bellows, et al.Epilepsia|April 11, 2023
Recognition and epileptology of protracted CLN3 diseaseJillian M Cameron, John A Damiano, Bronwyn Grinton, et al.Journal of Medical Genetics|October 26, 2010
Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patientsLaura K Conlin, Whitney Kramer, Anne L Hutchinson, et al.Epilepsia|April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsyAilsa McLellan, Hilary A Phillips, Christopher Rittey, et al.Archives of Neurology|January 14, 2009
Translational research in epilepsy genetics: sodium channels in man to interneuronopathy in mouseSaul A Mullen, Ingrid E SchefferCurrent Opinion in Neurology|February 15, 2013
Epilepsy classification: a cycle of evolution and revolutionChristian M Korff, Ingrid E SchefferPageof 73