CORTINI, FRANCESCA

CORTINI, FRANCESCA  

Dipartimento di Scienze Cliniche e di Comunità  

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Risultati 1 - 20 di 90 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
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 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) -
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) -
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) -
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) -
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 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) -
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) -
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) -
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) -
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype 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 2011 D. GalimbertiC. VillaL. GhezziA. PietroboniC. FenoglioF. CortiniM. SerpenteC. CantoniE. RidolfiF. JaciniA. ArighiN. BresolinE. 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. FenoglioF. CortiniM. SerpenteC. CantoniC. MarianiN. BresolinE.A. ScarpiniD. Galimberti + Article (author) -
Novel progranulin mutation in a sporadic case of frontotemporal dementia parkinsonism presentino with asymmetric rest tremor and cognitive decline 2011 D. GalimbertiF. CortiniC. CantoniE.A. 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 OLR1 and its regulating hsa-miR369-3p in Alzheimer’s disease : genetic and expression analysis 2011 D. GalimbertiM. SerpenteC. FenoglioC. VillaF. CortiniC. CantoniE. RidolfiC. MarianiN. BresolinE.A. Scarpini + Article (author) -
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred 2011 A.M. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoS.P. CortiN. BresolinD. GalimbertiE. Scarpini + Article (author) -