RIDOLFI, ELISA

RIDOLFI, ELISA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Mostra records
Risultati 1 - 20 di 34 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
C9ORF72 repeat expansion not detected in patients with multiple sclerosis 2014 C. FenoglioM. De RizM. SerpenteE. RidolfiR. BonsiA. PietroboniA. CalviE. ScarpiniD. Galimberti + Article (author) -
The role of the innate immune system in Alzheimer's disease and frontotemporal lobar degeneration : an eye on microglia 2013 E. RidolfiD. Galimberti + Article (author) -
An emerging role for long non-coding RNA dysregulation in neurological disorders 2013 C. FenoglioE. RidolfiD. 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 2013 E. RidolfiC. FenoglioL. GhezziM. SerpenteC. CantoniR. BonsiS. CioffiC. MarianiE. ScarpiniD. Galimberti + Article (author) -
Expression and genetic analysis of microRNAs involved in multiple sclerosis 2013 E. RidolfiC. FenoglioC. CantoniA. CalviM. De RizA. PietroboniM. SerpenteR. BonsiD. GalimbertiE. Scarpini + Article (author) -
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis 2013 C. FenoglioE. RidolfiC. CantoniM. De RizR. BonsiM. 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 2013 Villa, ChiaraRidolfi, ElisaFenoglio, ChiaraSerpente, MariaCantoni, ClaudiaBonsi, RossanaCioffi, SaraMariani, ClaudioScarpini, ElioGalimberti, Daniela + Article (author) -
TMEM106B genetic variability in patients with Alzheimer’s disease 2012 M. SerpenteC. FenoglioR. BonsiE. RidolfiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia 2012 D. GalimbertiB. Dell'OssoC. FenoglioC. VillaF. CortiniM. SerpenteC. CantoniE. RidolfiL. GhezziN. BresolinA.C. AltamuraE. Scarpini + Article (author) -
MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers 2012 F. Martinelli-BoneschiC. FenoglioM. SerpenteC. CantoniE. RidolfiM. De RizE. ScarpiniG. ComiD. Galimberti + Article (author) -
Decreased circulating miRNAs in patients with multiple sclerosis 2012 C. FenoglioE. RidolfiM. SerpenteN. BresolinD. GalimbertiE. Scarpini + Article (author) -
MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis 2012 C. FenoglioE. RidolfiD. GalimbertiE. Scarpini Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 2012 Villa, ChiaraGhezzi, LauraFenoglio, ChiaraSerpente, MariaCantoni, ClaudiaRidolfi, ElisaBonsi, RossanaMariani, ClaudioBresolin, NereoScarpini, ElioGalimberti, Daniela + Article (author) -
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration 2012 C. VillaL. GhezziC. FenoglioM. SerpenteC. CantoniE. RidolfiR. BonsiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
Role of OLR1 and its regulating has-miR369-3p in Alzheimer’s disease: genetic and expression analysis 2011 D. GalimbertiM. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -
GSK3β genetic variability in patients with Multiple Sclerosis 2011 D. GalimbertiD. ScalabriniC. FenoglioM.A. De RizF. CortiniC. VillaM. SerpenteC. CantoniE. RidolfiN. BresolinE.A. Scarpini + Article (author) -
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer’s disease : genetics and expression analysis 2011 M. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiC. MarianiN. BresolinE. ScarpiniD. Galimberti + Article (author) -
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease 2011 E. VenturelliC. VillaC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Causal frontotemporal de generation mutations : a novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia 2011 C. VillaL. GhezziA.M. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. jaciniA. ArighiA. MandelliN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
OLR1 and its regulatory miR-369-3p : genetics and expression analysis 2011 M. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -