Ictal ontogeny in Dravet syndrome

Clinical Neurophysiology

Volumn 126, Issue 3, 2015, Pages 446-455

  Kim, Se Hee ^a   Nordli, Douglas R ^a   Berg, Anne T ^a   Koh, Sookyong ^a   Laux, Linda ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Channelopathy; Epilepsy; Postictal generalized EEG suppression (PGES); SCN1A; Sudden unexpected death in epilepsy (SUDEP)

Indexed keywords

SODIUM CHANNEL NAV1.1; SCN1A PROTEIN, HUMAN;

ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE DURATION; ELECTROENCEPHALOGRAM; ELECTROENCEPHALOGRAPHY; EPILEPTIC DISCHARGE; FEMALE; FOCAL EPILEPSY; GENE MUTATION; HEAT; HUMAN; ICTAL ONTOGENY; MALE; MYOCLONUS SEIZURE; NEWBORN; ONTOGENY; PHOTOSENSITIVITY; PHOTOSTIMULATION; PRIORITY JOURNAL; SCHOOL CHILD; SEVERE MYOCLONIC EPILEPSY IN INFANCY; SPIKE; SPIKE WAVE; SYMPTOM; TONIC CLONIC SEIZURE; VIDEORECORDING; ADOLESCENT; BRAIN CORTEX; COMPLICATION; GENETICS; INFANT; MYOCLONUS EPILEPSY; PATHOPHYSIOLOGY; PRESCHOOL CHILD; SEIZURE; SUDDEN DEATH; YOUNG ADULT;

ADOLESCENT; CEREBRAL CORTEX; CHILD; CHILD, PRESCHOOL; DEATH, SUDDEN; ELECTROENCEPHALOGRAPHY; EPILEPSIES, MYOCLONIC; FEMALE; HUMANS; INFANT; MALE; NAV1.1 VOLTAGE-GATED SODIUM CHANNEL; SEIZURES; YOUNG ADULT;

EID: 84922560290     PISSN: 13882457     EISSN: 18728952     Source Type: Journal    
DOI: 10.1016/j.clinph.2014.06.024     Document Type: Article

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