RIDOLFI, ELISA

RIDOLFI, ELISA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 33 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
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) -
A sporadic case of progressive non-fluent aphasia caused by a novel progranulin mutation 1-gen-2011 E. RidolfiE.A. ScarpiniD. Galimberti + Article (author) -
An emerging role for long non-coding RNA dysregulation in neurological disorders 1-ott-2013 C. FenoglioE. RidolfiD. GalimbertiE. 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 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) -
Causal frontotemporal de generation mutations : 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) -
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype 1-gen-2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis 1-gen-2013 C. FenoglioE. RidolfiC. CantoniM. De RizR. BonsiM. SerpenteC. VillaN. BresolinD. GalimbertiE. Scarpini + Article (author) -
Decreased circulating miRNAs in patients with multiple sclerosis 1-ott-2012 C. FenoglioE. RidolfiM. SerpenteN. BresolinD. GalimbertiE. Scarpini + Article (author) -
Effects of simulated altitude (normobaric hypoxia) on cardiorespiratory parameters and circulating endothelial precursors in healthy subjects 1-gen-2007 M.M. CiullaM. CortianaI. SilvestrisE. MatteucciE. RidolfiZANARDELLI, MADDALENAR. PaliottiA. CortelezziF. MagriniM.A. Desiderio + Article (author) -
Expression and genetic analysis of microRNAs involved in multiple sclerosis 1-mar-2013 E. RidolfiC. FenoglioC. CantoniA. CalviM. De RizA. PietroboniM. SerpenteR. BonsiD. GalimbertiE. Scarpini + Article (author) -
Expression and genetic analysis of miRNAs involved in CD4+cell activation in patients with multiple sclerosis 17-ott-2011 C. FenoglioM. De RizE. RidolfiF. CortiniM. SerpenteC. VillaN. BresolinD. GalimbertiE. Scarpini + Article (author) -
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with alzheimer's disease 1-gen-2013 E. RidolfiC. FenoglioL. GhezziM. SerpenteC. CantoniR. BonsiS. CioffiC. MarianiE. ScarpiniD. Galimberti + Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2012 C. VillaL. GhezziC. FenoglioM. SerpenteC. CantoniE. RidolfiR. BonsiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2012 Villa, ChiaraGhezzi, LauraFenoglio, ChiaraSerpente, MariaCantoni, ClaudiaRidolfi, ElisaBonsi, RossanaMariani, ClaudioBresolin, NereoScarpini, ElioGalimberti, Daniela + Article (author) -
GSK3β genetic variability in patients with Multiple Sclerosis 1-gen-2011 D. GalimbertiD. ScalabriniC. FenoglioM.A. De RizF. CortiniC. VillaM. SerpenteC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -
MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers 2-feb-2012 F. Martinelli-BoneschiC. FenoglioM. SerpenteC. CantoniE. RidolfiM. De RizE. ScarpiniG. ComiD. Galimberti + Article (author) -