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Myoclonus in genetic Alzheimer's disease due to presenilin-1 mutation.
Uccellini, Davide; Canafoglia, Laura; Franceschetti, Silvana; Stabile, Andrea; Catania, Marcella; Tagliavini, Fabrizio; Giaccone, Giorgio; Di Fede, Giuseppe.
Afiliação
  • Uccellini D; Neurology - Neurophysiology Unit, ASST dei Sette Laghi, Galmarini Tradate Hospital, Tradate 21049, Italy.
  • Canafoglia L; Integrated Diagnostics for Epilepsy, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. Electronic address: laura.canafoglia@istituto-besta.it.
  • Franceschetti S; Neurophysiopathology, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy. Electronic address: silvana.franceschetti@istituto-besta.it.
  • Stabile A; Epilepsy Unit, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Member of the ERN EpiCARE, Milan, Italy.
  • Catania M; Neurology 5/Neuropathology Unit, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Tagliavini F; Neurology 5/Neuropathology Unit, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Giaccone G; Neurology 5/Neuropathology Unit, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Di Fede G; Neurology 5/Neuropathology Unit, Department of Diagnostic and Technology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Clin Neurophysiol ; 156: 86-88, 2023 12.
Article em En | MEDLINE | ID: mdl-37897907
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article