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Pediatric Neurology|April 17, 2004
Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancyBerten P G M Ceulemans, Lieve R F Claes, Lieven G LagaeHuman Mutation|July 9, 2009
The SCN1A variant database: a novel research and diagnostic toolLieve R F Claes, Liesbet Deprez, Arvid Suls, et al.Human Genetics|November 8, 2005
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutationLiesbet Deprez, Lieve R F Claes, Kristl G Claeys, et al.Seizure|April 4, 2007
Epilepsy and migraine in a patient with Urbach-Wiethe diseaseKristl G Claeys, Lieve R F Claes, Johan W M Van Goethem, et al.Epilepsia|November 22, 2007
Epilepsy as part of the phenotype associated with ATP1A2 mutationsLiesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, et al.Plos Genetics|September 19, 2009
A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndromeNanda A Singh, Chris Pappas, E Jill Dahle, et al.Annals of Neurology|October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2009
A functional null mutation of SCN1B in a patient with Dravet syndromeGustavo A Patino, Lieve R F Claes, Luis F Lopez-Santiago, et al.Human Mutation|July 26, 2006
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patientsArvid Suls, Kristl G Claeys, Dirk Goossens, et al.Annals of Neurology|January 26, 2012
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathySarah Weckhuysen, Simone Mandelstam, Arvid Suls, et al.Pageof 2