SERPENTE, MARIA

SERPENTE, MARIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 103 (tempo di esecuzione: 0.006 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
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 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 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 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 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 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 D. GalimbertiC. VillaL. GhezziA. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiN. BresolinE. Scarpini + 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) -
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) -
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation 1-gen-2022 Arighi, AndreaArcaro, MarinaFumagalli, Giorgio GiulioCarandini, TizianaPietroboni, Anna MargheritaSacchi, LucaFenoglio, ChiaraSerpente, MariaSorrentino, FedericaScarpini, ElioGalimberti, Daniela + Article (author) -
Association between enlarged perivascular spaces and cerebrospinal fluid aquaporin-4 and tau levels: report from a memory clinic 1-gen-2023 Sacchi, LucaArcaro, MarinaCarandini, TizianaPietroboni, Anna MargheritaFumagalli, Giorgio GiulioFenoglio, ChiaraSerpente, MariaSorrentino, FedericaVisconte, CaterinaConte, GiorgioScarpini, ElioTriulzi, FabioGalimberti, DanielaArighi, Andrea + 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) -
C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder 1-giu-2014 D. GalimbertiB. Dell'OssoC. FenoglioM. SerpenteA. AltamuraE. Scarpini + Article (author) -
C9ORF72 hexanucleotide repeat expansion frequency in patients with Paget's disease of bone 1-gen-2020 Galimberti D.Serpente M.Scarpini E.Fenoglio C. + Article (author) -
C9ORF72 repeat expansion not detected in patients with multiple sclerosis 1-gen-2014 C. FenoglioM. De RizM. SerpenteE. RidolfiR. BonsiA. PietroboniA. CalviE. ScarpiniD. Galimberti + Article (author) -
C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts 1-gen-2020 Galimberti, DanielaScarpini, ElioSerpente, Maria + Article (author) -
Candidate gene analysis of semaphorins in patients with Alzheimer's disease 1-gen-2010 C. VillaE. VenturelliC. FenoglioM. De RizD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinE. ScarpiniD. Galimberti Article (author) -