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MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian family.
Villa, Cristina; Rossi, Giacomina; Bizzozero, Ilaria; Prioni, Sara; Boiocchi, Chiara; Agosta, Federica; Canu, Elisa; Filippi, Massimo; Giaccone, Giorgio; Caroppo, Paola.
Afiliación
  • Villa C; Neurology V and Neuropathology Unit, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.
  • Rossi G; Neurology V and Neuropathology Unit, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.
  • Bizzozero I; Neurology V and Neuropathology Unit, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.
  • Prioni S; Clinical Neuropsychology Unit, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.
  • Boiocchi C; Neurology V and Neuropathology Unit, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.
  • Agosta F; Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Canu E; Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Filippi M; Vita-Salute San Raffaele University, Milan, Italy.
  • Giaccone G; Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Caroppo P; Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Eur J Neurol ; 29(5): 1529-1533, 2022 05.
Article en En | MEDLINE | ID: mdl-35020237

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Demencia Frontotemporal / Enfermedad de Alzheimer Límite: Humans / Male Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Demencia Frontotemporal / Enfermedad de Alzheimer Límite: Humans / Male Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Italia