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Ingrid E Scheffer

Showing results (461-470 of 586) with videos related to

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Epilepsia|February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history studyIngrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.
American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Annals of Neurology|March 28, 2020
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation LoadPiero Perucca, Alison Anderson, Dana Jazayeri, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Neurology|May 11, 2016
Definition and diagnostic criteria of sleep-related hypermotor epilepsyPaolo Tinuper, Francesca Bisulli, J H Cross, et al.
Epilepsia|March 17, 2022
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetamCiarán Campbell, Mark McCormack, Sonn Patel, et al.
Neurology|September 2, 2018
The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathyElena Gardella, Carla Marini, Marina Trivisano, et al.
Epilepsia Open|September 11, 2020
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study groupJoerg Klepper, Cigdem Akman, Marisa Armeno, et al.
Epilepsia|December 6, 2020
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disabilityAmy L Schneider, Candace T Myers, Alison M Muir, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathiesJacob E Munro, Harshini Thiyagarajah, Mark F Bennett, et al.
Pageof 59

Showing results (461-470 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia|February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history studyIngrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.
American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Annals of Neurology|March 28, 2020
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation LoadPiero Perucca, Alison Anderson, Dana Jazayeri, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Neurology|May 11, 2016
Definition and diagnostic criteria of sleep-related hypermotor epilepsyPaolo Tinuper, Francesca Bisulli, J H Cross, et al.
Epilepsia|March 17, 2022
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetamCiarán Campbell, Mark McCormack, Sonn Patel, et al.
Neurology|September 2, 2018
The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathyElena Gardella, Carla Marini, Marina Trivisano, et al.
Epilepsia Open|September 11, 2020
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study groupJoerg Klepper, Cigdem Akman, Marisa Armeno, et al.
Epilepsia|December 6, 2020
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disabilityAmy L Schneider, Candace T Myers, Alison M Muir, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathiesJacob E Munro, Harshini Thiyagarajah, Mark F Bennett, et al.
Pageof 59