VILLA, CHIARA

VILLA, CHIARA  

Universita' degli Studi di MILANO  

Mostra records
Risultati 1 - 20 di 62 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Forensic age estimation based on the trabecular bone changes of the pelvic bone using post-mortem CT 2013 C. VillaC. Cattaneo + Article (author) -
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) -
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) -
Common and unusual urogenital Crohn's disease complications : spectrum of cross-sectional imaging findings 2013 C. VillaA. CampariA. RavelliG. Cornalba + 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 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) -
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) -
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 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) -
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) -
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) -
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 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 : 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 against sporadic Frontotemporal Lobar Degeneration 2010 D. GalimbertiC. VillaC. FenoglioN. BresolinC. MarianiE. Scarpini + Article (author) -