GALIMBERTI, DANIELA

GALIMBERTI, DANIELA  

Dipartimento di Scienze Biomediche, Chirurgiche ed Odontoiatriche  

Risultati 1 - 20 di 578 (tempo di esecuzione: 0.215 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation 13-nov-2012 L. GhezziE. ScarpiniM. RangoA. ArighiM. De RizF. JaciniG.G. FumagalliA.M. PietroboniD. GalimbertiN. Bresolin + Article (author) -
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) -
A sporadic case of progressive non-fluent aphasia caused by a novel progranulin mutation 1-gen-2011 E. RidolfiE.A. ScarpiniD. Galimberti + Article (author) -
A91V variation of the perforin gene in patients with multiple sclerosis 1-gen-2006 D. GalimbertiC. FenoglioE. Scarpini + Article (author) -
ABCA1- And ABCG1-mediated cholesterol efflux capacity of cerebrospinal fluid is impaired in Alzheimer's disease 1-ago-2019 Galimberti D. + Article (author) -
Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort 5-ago-2020 Galimberti, Daniela + 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 TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration 1-gen-2009 E.A. ScarpiniD. GalimbertiE. Venturelli + 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) -
Accuracy of the clinical diagnosis of dementia with Lewy bodies (DLB) among the Italian Dementia Centers: a study by the Italian DLB study group (DLB-SINdem) 4-mar-2022 Galimberti, DanielaSilani, Vincenzo + 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) -
Alemtuzumab in multiple sclerosis during the COVID-19 pandemic: A mild uncomplicated infection despite intense immunosuppression 1-gen-2020 Carandini T.Pietroboni A. M.De Riz M. A.Pozzato M.Arighi A.Fumagalli G. G.Martinelli Boneschi F.Galimberti D.Scarpini E. + Article (author) -
Alpha-MSH peptides inhibit production of nitric oxide and tumor necrosis factor-alpha by microglial cells activated with beta-amyloid and interferon gamma 1-gen-1999 D. GalimbertiE. Scarpini + Article (author) -
Alpha1-antichymotrypsin induces TNF-alpha production and NF-kappaB activation in the murine N9 microglial cell line 1-gen-2009 BRAGHIN, ELISA GAIA ALESSANDRAD. GalimbertiE. ScarpiniN. Bresolin + Article (author) -
Alzheimer's Disease : From Pathogenesis to Disease-Modifying Approaches 1-gen-2011 D. GalimbertiE.A. Scarpini 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) -
An APOE Haplotype Associated with Decreased ε4 Expression Increases the Risk of Late Onset Alzheimer's Disease 1-gen-2011 D. GalimbertiE.A. Scarpini + Article (author) -