Outcomes and comorbidities of SCN1A-related seizure disorders

I.M. de Lange, B. Gunning, A.C.M. Sonsma, L. van Gemert, M. van Kempen, N.E. Verbeek, C. Sinoo, J. Nicolai, N.V.A.M. Knoers, B.P.C. Koeleman, E.H. Brilstra

Research output: Contribution to journalArticleAcademicpeer-review

16 Citations (Web of Science)
Original languageEnglish
Pages (from-to)252-259
Number of pages8
JournalEpilepsy & Behavior
Volume90
DOIs
Publication statusPublished - 1 Jan 2019

Keywords

  • behavior
  • behavioral problems
  • children
  • comorbidities
  • dravet
  • dravet-syndrome
  • gefs
  • mutation
  • quality-of-life
  • reduced sodium current
  • scn1a
  • scn1a gene
  • severe myoclonic epilepsy
  • spectrum
  • variants
  • GEFS
  • Behavioral problems
  • MUTATION
  • QUALITY-OF-LIFE
  • SPECTRUM
  • SCN1A
  • REDUCED SODIUM CURRENT
  • VARIANTS
  • BEHAVIOR
  • Dravet
  • CHILDREN
  • SCN1A GENE
  • Comorbidities
  • DRAVET-SYNDROME
  • SEVERE MYOCLONIC EPILEPSY

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