GALIMBERTI, DANIELA

GALIMBERTI, DANIELA  

Dipartimento di Scienze Biomediche, Chirurgiche ed Odontoiatriche  

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Risultati 1 - 20 di 635 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A "Candidate-Interactome" Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis 1-gen-2013 V.A..G. RiciglianoB. Filippo MartinelliG. ComiD. CusiD. GalimbertiF.R. GueriniS. LupoliF. MacciardiE. Salvi + Article (author) -
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 C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers 1-ott-2018 Galimberti, DanielaScarpini, Elio + Article (author) -
A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation 1-gen-2012 L. GhezziD. GalimbertiN. BresolinE. Scarpini + Article (author) -
A case of bipolar disorder developing into atypical parkinsonism and presenting with frontotemporal asymmetrical brain degeneration : A TREDEM Registry Case Report 1-mar-2020 Galimberti D.Serpente M. + Article (author) -
A case of vanishing white-matter disease due to the c.260C>T (p.Ala87Val) EIF2B3 mutation 1-gen-2012 L. GhezziD. GalimbertiN. BresolinE. Scarpini + Article (author) -
A Case with Early Onset Alzheimer's Disease, Frontotemporal Hypometabolism, ApoE Genotype ϵ 4/ ϵ 4 and C9ORF72 Intermediate Expansion : A Treviso Dementia (TREDEM) Registry Case Report 1-gen-2019 Fenoglio, ChiaraSerpente, MariaGalimberti, Daniela + Article (author) -
A critical review on structural neuroimaging studies in BD : a transdiagnostic perspective from psychosis to fronto-temporal dementia 1-giu-2020 Delvecchio G.Squarcina L.Arighi A.Galimberti D.Scarpini E.Brambilla P. + Article (author) -
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia 1-gen-2022 Galimberti D.Scarpini E. + 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 genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 1-ott-2015 E. SalviD. GalimbertiE. ScarpiniM. Serpente + Article (author) -
A high throughput, multiplexed and targeted proteomic CSF assay to quantify neurodegenerative biomarkers and apolipoprotein E isoforms status 1-gen-2016 D. Galimberti + Article (author) -
A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases : CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD 1-gen-2013 D. Galimberti + Article (author) -
A multicentre validation study of the diagnostic value of plasma neurofilament light 1-gen-2021 Galimberti D. + Article (author) -
A new helpful tool for the diagnosis of different cognitive disorders 1-gen-2005 S. LonatiC. NovembrinoI. GuidiD. GalimbertiG. Lambertenghi-DeliliersF. Bamonti + Article (author) -
A new method to discriminate among different memory disorders 1-gen-2005 I. GuidiC. NovembrinoS. LonatiD. GalimbertiE. ScarpiniG. Lambertenghi-DeliliersF. Bamonti + Article (author) -
A Novel Automated Chemiluminescence Method for Detecting Cerebrospinal Fluid Amyloid-Beta 1-42 and 1-40, Total Tau and Phosphorylated-Tau: Implications for Improving Diagnostic Performance in Alzheimer’s Disease 1-gen-2022 Arcaro, MarinaFenoglio, ChiaraSerpente, MariaArighi, AndreaFumagalli, Giorgio G.Sacchi, LucaFloro, StefanoD’Anca, MariannaSorrentino, FedericaVisconte, CaterinaScarpini, ElioGalimberti, Daniela + Article (author) -
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 1-gen-2011 Ghezzi, LauraPietroboni, Anna M.Fenoglio, ChiaraCortini, FrancescaSerpente, MariaCantoni, ClaudiaRidolfi, ElisaJacini, FrancescaArighi, AndreaFumagalli, Giorgio G.Bresolin, NereoScarpini, ElioGalimberti, Daniela + Article (author) -
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) -
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 1-gen-2011 D. GalimbertiL. GhezziC. FenoglioM. SerpenteE. RidolfiN. BresolinE. Scarpini + Article (author) -