Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation

Matteo Cataldi, Lino Nobili, Federico Zara, Romina Combi, Giulia Prato, Thea Giacomini, Valeria Capra, Patrizia De Marco, Luigi Ferini-Strambi, Maria Margherita Mancardi

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)57-60
Number of pages4
JournalSeizure
Volume67
DOIs
Publication statusPublished - Apr 2019

Keywords

  • Child, Preschool
  • Epilepsies, Partial/diagnosis
  • Humans
  • Male
  • Mutation
  • Nerve Tissue Proteins/genetics
  • Parasomnias/diagnosis
  • Pedigree
  • Potassium Channels, Sodium-Activated/genetics

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