FENOGLIO, CHIARA

FENOGLIO, CHIARA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Risultati 1 - 20 di 294 (tempo di esecuzione: 0.002 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
A functional variant in ERAP1 predisposes to multiple sclerosis 1-gen-2012 D. GalimbertiC. FenoglioM. BiasinR. AsseltaE. ScarpiniG.P. ComiN. BresolinM.S. Clerici + Article (author) -
A91V variation of the perforin gene in patients with multiple sclerosis 1-gen-2006 D. GalimbertiC. FenoglioE. Scarpini + Article (author) -
Absence of mutations in TREM-2 coding region in early onset dementia 1-gen-2006 C. FenoglioD. GalimbertiE. VenturelliL. PiccioD. ScalabriniC. MarianiN. BresolinE. Scarpini + Article (author) -
Absence of mutations in TREM-2 coding region in early onset dementia 3-lug-2007 C. FenoglioD. GalimbertiE. VenturelliL. PiccioD. ScalabriniC. MarianiN. BresolinE. Scarpini + Conference Object -
Absence of mutations in TREM-2 coding region in patients with early onset dementia 1-gen-2006 C. FenoglioD. GalimbertiE. VenturelliL. PiccioD. ScalabriniC. LovatiC. MarianiN. BresolinE. Scarpini + Article (author) -
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration 1-gen-2007 C. FenoglioD. GalimbertiL. PiccioD. ScalabriniE. VenturelliC. LovatiC. MarianiN. BresolinE. Scarpini + Article (author) -
Age at symptom onset and death and disease duration in genetic frontotemporal dementia : an international retrospective cohort study 1-gen-2020 Galimberti D.Scarpini E.Fumagalli G. G.Arighi A.Fenoglio C. + Article (author) -
Alzheimer's disease: from pathogenesis to new perspectives for treatment 1-gen-2008 D.GALIMBERTIC.FENOGLIOE.SCARPINI Book Part (author) -
Amyloid PET as a marker of normal-appearing white matter early damage in multiple sclerosis : correlation with CSF β-amyloid levels and brain volumes 1-gen-2019 Pietroboni, Anna M.Carandini, TizianaColombi, AnnalisaMercurio, MatteoGhezzi, LauraScarioni, MartaArighi, AndreaFenoglio, ChiaraDe Riz, Milena A.Fumagalli, Giorgio G.Basilico, PaolaSerpente, MariaScarpini, ElioGalimberti, Daniela + Article (author) -
Analysis of C9orf72 Intermediate Alleles in a Retrospective Cohort of Neurological Patients: Risk Factors for Alzheimer's Disease? 1-gen-2021 Serpente M.Fenoglio C.Sorrentino F.Scarpini E.Galimberti D. + Article (author) -
Anti-Cholinergic Derangement of Cortical Metabolism on 18F-FDG PET in a Patient with Frontotemporal Lobar Degeneration Dementia : a Case of the TREDEM Registry 1-gen-2020 Fenoglio C.Serpente M.Galimberti D. + Article (author) -
ApoE e2 and e4 influence the susceptibility for Alzheimer’s disease but not other dementias 1-gen-2007 D. GalimbertiC. LovatiP. BertoraE. VenturelliI. GuidiC. FenoglioF. CortiniN. BresolinC. MarianiE. Scarpini + Article (author) -
ApoE e2 decreases the susceptibility to develop Alzheimer's disease but not frontotemporal lobar degeneration, Lewy body disease or vascular dementia 1-mar-2007 D. GalimbertiC. LovatiE. VenturelliP. BertoraI. GuidiC. FenoglioF. CortiniN. BresolinC. MarianiE. Scarpini + Article (author) -
Association between Alzheimer’s disease and the hypocretin receptor 2 gene 1-gen-2011 D. GalimbertiC. FenoglioE. Scarpini + Article (author) -
Association between VEGF gene and sporadic Alzheimer's disease. 1-gen-2005 R. Del BoF. Martinelli-BoneschiC. FenoglioR. VirgilioD. GalimbertiM. CrimiE. ScarpiniN. BresolinG.P. Comi + Book Part (author) -
Association between VEGF gene and sporadic Alzheimer’s Disease 1-gen-2005 R. Del BoF. Martinelli BoneschiC. FenoglioR. VirgilioD. GalimbertiM. CrimiE. ScarpiniN. BresolinG.P. Comi + Article (author) -
Association of neuronal nitric oxide synthase C276T polymorphism with Azheimer's disease 1-gen-2005 A. GattiD. GalimbertiC. LovatiC. FenoglioE. VenturelliC. MarianiN. BresolinE. Scarpini + Article (author) -
Association study to evaluate the serotonin trasporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy 1-dic-2008 C. FenoglioD. GalimbertiC. MarianiE. Scarpini + Article (author) -
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) -
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease 1-gen-2011 E. VenturelliC. VillaC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -