Showing results (1-10 of 63) with videos related to
Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|November 26, 2015
Lessons learned from gene identification studies in Mendelian epilepsy disordersKatia Hardies, Sarah Weckhuysen, Peter De Jonghe, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|August 26, 2011
"Benign" myoclonic epilepsy of infancy as the initial presentation of glucose transporter-1 deficiencyNicolas Gaspard, Arvid Suls, Catheline Vilain, et al.Epilepsia|April 6, 2011
The genetics of Dravet syndromeCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.Neurology|September 20, 2013
Duplications of 17q12 can cause familial fever-related epilepsy syndromesKatia Hardies, Sarah Weckhuysen, Elke Peeters, et al.Journal of the Peripheral Nervous System : JPNS|September 14, 2012
A novel autosomal dominant GDAP1 mutation in an Italian CMT2 familyFiore Manganelli, Chiara Pisciotta, Maria Nolano, et al.Developmental Medicine and Child Neurology|June 15, 2013
Head stereotypies in STXBP1 encephalopathyYoung Ok Kim, Christian M Korff, Mel Michel G Villaluz, et al.Epilepsia|January 6, 2011
Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiencyZaid Afawi, Arvid Suls, Dana Ekstein, et al.Cancer Medicine|April 18, 2019
Methylation analysis of Gasdermin E shows great promise as a biomarker for colorectal cancerJoe Ibrahim, Ken Op de Beeck, Erik Fransen, et al.Human Mutation|July 9, 2009
The SCN1A variant database: a novel research and diagnostic toolLieve R F Claes, Liesbet Deprez, Arvid Suls, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2011
Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutationLubov Blumkin, Arvid Suls, Tine Deconinck, et al.Pageof 7