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
Transperineal perineal ultrasound versus magnetic resonance imaging in the assessment of perianal Crohn's disease 2013 G. MaconiM. MonteleoneC. BezzioF. FurfaroC. VillaA. DellʼEraS. ArdizzoneR. de Franchis + Article (author) -
Common and unusual urogenital Crohn's disease complications : spectrum of cross-sectional imaging findings 2013 C. VillaA. CampariA. RavelliG. Cornalba + Article (author) -
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion : late-onset psychotic clinical presentation 2013 D. GalimbertiC. FenoglioM. SerpenteC. VillaR. BonsiA. ArighiG.G. FumagalliR. Del BoB. Dell'OssoG.P. ComiA.C. AltamuraC. MarianiE. Scarpini + Article (author) -
Forensic age estimation based on the trabecular bone changes of the pelvic bone using post-mortem CT 2013 C. VillaC. Cattaneo + Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 2012 C. VillaL. GhezziC. FenoglioM. SerpenteC. CantoniE. RidolfiR. BonsiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia 2012 D. GalimbertiB. Dell'OssoC. FenoglioC. VillaF. CortiniM. SerpenteC. CantoniE. RidolfiL. GhezziN. BresolinA.C. AltamuraE. Scarpini + Article (author) -
Role of OLR1 and its regulating has-miR369-3p in Alzheimer’s disease: genetic and expression analysis 2011 D. GalimbertiM. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -
Oligodendrocyte Lineage Transcription Factor 2 role in Alzheimer’s disease : association and expression analysis 2011 F. CortiniC. FenoglioC. VillaM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Causal frontotemporal de generation mutations : a novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. jaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Oligodendrocyte lineage transcription factor-2 role in Alzheimer’s disease : association and expression analysis 2011 F. CortiniC. FenoglioC. VillaM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
OLR1 and its regulatory miR-369-3p : genetics and expression analysis 2011 M. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype 2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 2011 D. GalimbertiC. VillaL. GhezziA. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiN. BresolinE. Scarpini + Article (author) -
Role of hnRNP-A1 and miR-590-3p in neuronal death : genetics and expression analysis in patients with Alzheimer’s disease and frontotemporal lobar degeneration 2011 E. RidolfiC. VillaC. FenoglioM.A. De RizF. CortiniM. SerpenteC. CantoniF. Martinelli BoneschiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer’s disease : genetic and expression analysis 2011 D. GalimbertiM. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiC. MarianiN. BresolinE.A. Scarpini + Article (author) -
GSK3β genetic variability in patients with Multiple Sclerosis 2011 D. GalimbertiD. ScalabriniC. FenoglioM.A. De RizF. CortiniC. VillaM. SerpenteC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer’s disease : genetics and expression analysis 2011 M. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Role of hnRNP-A1 and miR-590-3p in Neuronal Death : Genetics and Expression Analysis in Patients with Alzheimer Disease and Frontotemporal Lobar Degeneration 2011 C. VillaC. FenoglioM.A. De RizF. CortiniM. SerpenteC. CantoniC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
CHMP5 and BAG1 are protective factors for sporadic frontotemporal lobar degeneration 2010 D. GalimbertiC. VillaE. VenturelliC. FenoglioD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinC. MarianiE. Scarpini + Article (author) -