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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.
Afiliação
  • 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 em En | MEDLINE | ID: mdl-35020237

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Demência Frontotemporal / Doença de Alzheimer Limite: Humans / Male Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Demência Frontotemporal / Doença de Alzheimer Limite: Humans / Male Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália