When is a child with status epilepticus likely to have Dravet syndrome?

Epilepsy Research

Volumn 108, Issue 4, 2014, Pages 740-747

  Le Gal, François ^a   Lebon, Sébastien ^b   Ramelli, Gian Paolo ^c   Datta, Alexandre N ^d   Mercati, Danielle ^e   Maier, Oliver ^f   Combescure, Christophe ^g   Rodriguez, Maria Isabel ^a   Seeck, Margitta ^a   Roulet, Eliane ^b   Korff, Christian M ^a  

^a University Hospital   (Switzerland)

^b LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^c Regional Hospital   (Switzerland)

^d UNIVERSITY HOSPITAL BASEL   (Switzerland)

^e Pediatric Neurology   (Switzerland)

^f Paediatric Emergency Medicine   (Switzerland)

^g UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

Children; SCN1A; Status epilepticus

Indexed keywords

SODIUM CHANNEL NAV1.1; SCN1A PROTEIN, HUMAN;

ADOLESCENT; ARTICLE; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; EPILEPTIC STATE; FEBRILE CONVULSION; FEMALE; FRAMESHIFT MUTATION; GENERALIZED EPILEPSY; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NONSENSE MUTATION; ONSET AGE; PRIORITY JOURNAL; RECURRENT DISEASE; RISK ASSESSMENT; RNA SPLICING; SCN1A GENE; SEVERE MYOCLONIC EPILEPSY IN INFANCY; COMPLICATION; DIFFERENTIAL DIAGNOSIS; EPILEPSIES, MYOCLONIC; GENETICS; INFANT; MUTATION; PRESCHOOL CHILD; STATUS EPILEPTICUS;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; EPILEPSIES, MYOCLONIC; FEMALE; HUMANS; INFANT; MALE; MUTATION; NAV1.1 VOLTAGE-GATED SODIUM CHANNEL; STATUS EPILEPTICUS;

EID: 84898047101     PISSN: 09201211     EISSN: 18726844     Source Type: Journal    
DOI: 10.1016/j.eplepsyres.2014.02.019     Document Type: Article

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