CORTINI, FRANCESCA

CORTINI, FRANCESCA  

Dipartimento di Scienze Cliniche e di Comunità  

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Risultati 1 - 20 di 90 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A Rare Cause of Juvenile Stroke: Extracranial Carotid Artery Aneurysm with Venous Complete Reconstruction of the Carotid Bifurcation 2018 Domanin, MaurizioLanfranconi, SilviaRomagnoli, SilviaCortini, FrancescaComi, Giacomo PieroGabrielli, Livio + Article (author) -
PICALM gene methylation in blood of Alzheimer's disease patients is associated with cognitive decline 2018 Mercorio, RobertaPergoli, LauraGalimberti, DanielaFavero, ChiaraCarugno, MicheleDalla Valle, ElisabettaBarretta, FrancescoCortini, FrancescaScarpini, ElioBollati, ValentinaPesatori, Angela Cecilia Article (author) -
A New COL3A1 Mutation in Ehlers-Danlos Syndrome Vascular Type with Different Phenotypes in the Same Family 2017 F. CortiniB. MarinelliA.C. PesatoriN. Montano + Article (author) -
Repetitive element hypermethylation in multiple sclerosis patients 2016 F. CortiniC. FenoglioD. GalimbertiA.C. PesatoriE. ScarpiniV. Bollati + Article (author) -
Effects of particulate matter exposure on multiple sclerosis hospital admission in Lombardy region, Italy 2016 F. CortiniA.C. PesatoriV. Bollati + Article (author) -
Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case report 2016 F. CortiniB. MarinelliB. De GiorgioA.C. PesatoriN. Montano + Article (author) -
Bone involvement in adult patients affected with Ehlers-Danlos syndrome 2016 Eller-Vainicher, C.BASSOTTI, ALESSANDRA FRANCESCAIMERAJ, AMANTIACairoli, E.Cortini, F.DUBINI, MARCOMARINELLI, ELOISA BRUNILDE LINASpada, A.Chiodini, I. + 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) -
Role of hnRNP-A1 and miR-590-3p in neuronal death : genetics and expression analysis in patients with Alzheimer’s disease and frontotemporal lobar degeneration 2011 E. RidolfiC. VillaC. FenoglioM.A. De RizF. CortiniM. SerpenteC. CantoniF. Martinelli BoneschiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Role of hnRNP-A1 and miR-590-3p in neuronal death : genetics and expression analysis in patients with Alzheimer’s disease and Frontotemporal Lobar Degeneration 2011 E. RidolfiC. FenoglioF. CortiniM. SerpenteC. CantoniC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Expression and genetic analysis of miRNAs involved in CD4+cell activation in patients with multiple sclerosis 2011 C. FenoglioM. De RizE. RidolfiF. CortiniM. SerpenteC. VillaN. BresolinD. GalimbertiE. Scarpini + Article (author) -
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease 2011 F. CortiniC. FenoglioE. VenturelliC. VillaM. SerpenteC. CantoniC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Phenotypic heterogeneity of the progranulin gene Asp22fs mutation in a large Italian kindred 2011 A.M. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoS.P. CortiN. BresolinD. GalimbertiE.A. Scarpini + Article (author) -
Role of hnRNP-A1 and miR-590-3p in Neuronal Death : Genetics and Expression Analysis in Patients with Alzheimer Disease and Frontotemporal Lobar Degeneration 2011 C. VillaC. FenoglioM.A. De RizF. CortiniM. SerpenteC. CantoniC. MarianiN. BresolinE.A. 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) -
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) -
Cognitive decline and extrapyramidal features in a sporadic case of Frontotemporal dementia-parkinsonism caused by a novel progranulin mutation 2011 D. GalimbertiF. CortiniC. CantoniE.A. Scarpini + 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) -
Oligodendrocyte lineage transcription factor-2 role in Alzheimer’s disease : association and expression analysis 2011 F. CortiniC. FenoglioC. VillaM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Oligodendrocyte Lineage Transcription Factor 2 role in Alzheimer’s disease : association and expression analysis 2011 F. CortiniC. FenoglioC. VillaM. SerpenteC. CantoniE. RidolfiC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -