VILLA, CHIARA

VILLA, CHIARA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 62 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Anthropological and paleopathological study of middle age human skeletal remains from Fara Gera d'Adda (Bergamo, Northern Italy) 1-gen-2008 C. VILLAA. MAZZUCCHIC. CATTANEO Conference Object -
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion : late-onset psychotic clinical presentation 1-set-2013 D. GalimbertiC. FenoglioM. SerpenteC. VillaR. BonsiA. ArighiG.G. FumagalliR. Del BoB. Dell'OssoG.P. ComiA.C. AltamuraC. MarianiE. Scarpini + Article (author) -
Candidate gene analysis of semaphorins in patients with Alzheimer's disease 1-gen-2010 C. VillaE. VenturelliC. FenoglioM. De RizD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinE. ScarpiniD. Galimberti Article (author) -
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis 1-gen-2007 D. ScalabriniC. FenoglioE. ScarpiniM. De RizE. VenturelliF. CortiniM. PiolaC. VillaN. BresolinD. Galimberti + Article (author) -
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) -
CDKN2A and CDKN2B genetic variability in Alzheimer's disease patients. 1-giu-2009 F. CortiniC. FenoglioE. VenturelliC. VillaD. ScalabriniC. MarianiN. BresolinE. ScarpiniD. Galimberti + Conference Object -
CHMP5 and BAG1 are protective factors against sporadic Frontotemporal Lobar Degeneration 1-gen-2010 D. GalimbertiC. VillaC. FenoglioN. BresolinC. MarianiE. Scarpini + Article (author) -
CHMP5 and BAG1 are protective factors for sporadic frontotemporal lobar degeneration 1-gen-2010 D. GalimbertiC. VillaE. VenturelliC. FenoglioD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinC. MarianiE. Scarpini + Article (author) -
Common and unusual urogenital Crohn's disease complications : spectrum of cross-sectional imaging findings 1-feb-2013 C. VillaA. CampariA. RavelliG. Cornalba + Article (author) -
DCUN1D1 is a risk factor for frontotemporal lobar degeneration 1-lug-2009 C. VillaE. VenturelliC. FenoglioD. ScalabriniF. CortiniF. Martinelli BoneschiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Expression profile of miRNAs involved in CD4+ lymphocyte activation and differentiation in patients with multiple sclerosis 1-gen-2010 D. GalimbertiC. FenoglioD. ScalabriniM. SerpenteC. CantoniM. De RizA. PietroboniM. PiolaE. VenturelliC. VillaF. CortiniN. BresolinE. Scarpini + Article (author) -
Forensic age estimation based on the trabecular bone changes of the pelvic bone using post-mortem CT 10-dic-2013 C. VillaC. Cattaneo + Article (author) -
Genetic and functional analysis of progranulin gene variants in Alzheimer's disease 1-gen-2008 C. FENOGLIOD. GALIMBERTIF. CORTINIE. VENTURELLII. GUIDID. SCALABRINIC. VILLAE. DALLA VALLEC. LOVATIC. MARIANIN. BRESOLINE. SCARPINI + Conference Object -
Genetic and functional analysis of progranulin gene variants in Alzheimer's disease. 1-gen-2008 C. FenoglioD. GalimbertiF. CortiniE. VenturelliD. ScalabriniC. LovatiC. VillaC. MarianiN. BresolinE. Scarpini + Article (author) -
Genetic and functional analysis of progranulin gene variants in patients with Alzheimer's disease 1-gen-2008 C. FenoglioF. CortiniE. VenturelliI. GuidiD. GalimbertiC. VillaE. Dalla ValleC. LovatiC. MarianiE. ScarpiniN. BresolinD. Scalabrini + Conference Object -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2012 C. VillaL. GhezziC. FenoglioM. SerpenteC. CantoniE. RidolfiR. BonsiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
GRN rs5848 in neurodegeneration: a role in axonal damage? 9-gen-2009 D. SCALABRINIC. FENOGLIOM. DE RIZLM. PICCIOE. VENTURELLIF. CORTINIC. VILLAM. PIOLAA. PIETROBONIN. BRESOLIND. GALIMBERTIE. SCARPINI + Conference Object -
GRN rs5848 polymorphism: a role in neurodegeneration? 1-giu-2009 D. ScalabriniC. FenoglioF. Martinelli BoneschiM. De RizE. VenturelliF. CortiniC. VillaM. PiolaN. BresolinD. GalimbertiE. Scarpini + Conference Object -
GSK3β genetic variability in patients with Multiple Sclerosis 1-gen-2011 D. GalimbertiD. ScalabriniC. FenoglioM.A. De RizF. CortiniC. VillaM. SerpenteC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -