MANDELLI, ALESSANDRA

MANDELLI, ALESSANDRA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Causal frontotemporal de generation mutations : a novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 1-gen-2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. jaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype 1-gen-2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
NOS3 Glu298Asp polymorphism is a risk factor for frontotemporal lobar degeneration 1-gen-2008 E. VENTURELLIC. VILLAC. FENOGLIOC. LOVATIR. GHIDONIF. CORTINID. SCALABRINIA. MANDELLIC. MARIANIN. BRESOLINE. SCARPINID. GALIMBERTI + Conference Object -
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 1-gen-2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Progranulin gene mutation scanning in Alzheimer's disease and Frontotemporal Lobar Degeneration: fuctional and phenotypic correlations 1-gen-2008 D. GALIMBERTIC. FENOGLIOF. CORTINIE. VENTURELLII. GUIDID. SCALABRINIC. VILLAA. MANDELLIS. POMATIC. MARIANIN. BRESOLINE. SCARPINI + Conference Object -
Progranulin gene mutation scanning in Alzheimer's disease and frontotemporal lobar degeneration: functional and phenotypic correlations. 1-giu-2008 E. VenturelliC. FenoglioF. CortiniD. ScalabriniC. VillaI. GuidiMANDELLI, ALESSANDRAPERINI, LUCAS. PomatiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -