ROTONDO, EMANUELA

ROTONDO, EMANUELA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Circulating Non-Coding RNA Levels Are Altered in Autosomal Dominant Frontotemporal Dementia 25-nov-2022 Fenoglio, ChiaraSerpente, MariaVisconte, CaterinaArcaro, MarinaSorrentino, FedericaD'Anca, MariannaArighi, AndreaRotondo, EmanuelaScarpini, ElioGalimberti, Daniela + Article (author) -
Detection of the SQSTM1 Mutation in a Patient with Early-Onset Hippocampal Amnestic Syndrome 1-gen-2021 Sacchi L.Ghezzi L.Pietroboni A. M.Fenoglio C.Arighi A.Fumagalli G. G.De Riz M. A.Serpente M.Rotondo E.Scarpini E.Galimberti D. + Article (author) -
Diogenes syndrome in dementia: a case report 1-mar-2021 Rotondo, EmanuelaPozzoli, SaraFiorentini, AlessioSchinco, GiuseppinaMandelli, ClaraFumagalli, Giorgio GCarandini, TizianaPietroboni, Anna MGalimberti, DanielaTriulzi, FabioScarpini, ElioCesari, MatteoBrambilla, PaoloArighi, Andrea + Article (author) -
GRN Asp22fs mutation is associated with highly variable age at onset, clinical phenotype and brain atrophy 1-gen-2010 A. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoP. CortiN. BresolinD. GalimbertiE. Scarpini + Article (author) -
miR-150-5p and let-7b-5p in Blood Myeloid Extracellular Vesicles Track Cognitive Symptoms in Patients with Multiple Sclerosis 1-gen-2022 Visconte, CaterinaSerpente, MariaGabrielli, MartinaCarandini, TizianaDe Riz, MilenaPietroboni, AnnaRotondo, EmanuelaScarpini, ElioGalimberti, DanielaFenoglio, Chiara + Article (author) -
miRNA Expression Is Increased in Serum from Patients with Semantic Variant Primary Progressive Aphasia 30-lug-2022 Serpente, MariaFenoglio, ChiaraBuccellato, Francesca RFumagalli, Giorgio GRotondo, EmanuelaArcaro, MarinaArighi, AndreaGalimberti, Daniela + Article (author) -
Niemann-Pick Type C 1 (NPC1) and NPC2 gene variability in demented patients with evidence of brain amyloid deposition 28-set-2021 Sorrentino F.Arighi A.Serpente M.Arosio B.Arcaro M.Visconte C.Rotondo E.Ferri E.Fumagalli G. G.Pietroboni A. M.Carandini T.Scarpini E.Fenoglio C.Galimberti D. + Article (author) -
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred 1-gen-2011 A.M. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoP. CortiN. BresolinD. GalimbertiE.A. Scarpini + Article (author) -
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred 1-gen-2011 A.M. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoS.P. CortiN. BresolinD. GalimbertiE. Scarpini + Article (author) -
Phenotypic heterogeneity of the progranulin gene Asp22fs mutation in a large Italian kindred 1-gen-2011 A.M. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoS.P. CortiN. BresolinD. GalimbertiE.A. Scarpini + Article (author) -
PROGRESSIONE DA MILD COGNITIVE IMPAIRMENT A MALATTIA DI ALZHEIMER: IDENTIFICAZIONE DI PROFILI NEUROCOGNITIVI PREDITTIVI E CORRELAZIONE CON BIOMARCATORI LIQUORALI 30-mag-2012 E. Rotondo Doctoral Thesis -
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort 1-dic-2020 Rotondo E.Galimberti D.Arighi A.Fenoglio C.Scarpini E.Fumagalli G. + Article (author) -
The Gut Microbiome-Brain Crosstalk in Neurodegenerative Diseases 1-gen-2022 Ghezzi, LauraCantoni, ClaudiaRotondo, EmanuelaGalimberti, Daniela Article (author) -