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

Uccellini, Davide; Canafoglia, Laura; Franceschetti, Silvana; Stabile, Andrea; Catania, Marcella; Tagliavini, Fabrizio; Giaccone, Giorgio; Di Fede, Giuseppe.

Afiliación

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 en En | MEDLINE | ID: mdl-37897907

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Neurophysiol Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia

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