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Author/Creator Arcaro, Marina

1. Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation. (12th December 2017)

Authors:
Ghezzi, Laura; Carandini, Tiziana; Arighi, Andrea; Fenoglio, Chiara; Arcaro, Marina; De Riz, Milena; Pietroboni, Anna M.; Fumagalli, Giorgio G.; Basilico, Paola; Calvi, Alberto; Scarioni, Marta; Colombi, Annalisa; Serpente, Maria; Marotta, Giorgio; Benti, Riccardo; Scarpini, Elio; Galimberti, Dan...
Journal:
Neurology
Issue:
Volume 89:Number 24(2017)
Page Start:
Record Type:
Journal Article
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2. Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation. Issue 3 (15th November 2016)

Authors:
Galimberti, Daniela; Cioffi, Sara M. G.; Fenoglio, Chiara; Serpente, Maria; Oblak, Adrian L.; Rodriguez‐Porcel, Federico; Oldoni, Emanuela; Hagen, Matthew C.; Arcaro, Marina; Scarpini, Elio; Ghetti, Bernardino; Espay, Alberto J.
Other Names:
Espay Alberto guestEditor.; Erro Roberto guestEditor.
Journal:
Movement disorders
Issue:
Volume 32:Issue 3(2017)
Page Start:
476
Record Type:
Journal Article
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