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Mostrati risultati da 1 a 20 di 43
Titolo Data di pubblicazione Autori Tipo File Abstract
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort 2010 F. Martinelli-BoneschiD. ScalabriniC. FenoglioM. SerpenteC. CantoniE. ScarpiniD. Galimberti + Article (author) -
GRN Asp22fs mutation is associated with heterogeneous neurodegenerative clinical phenotypes 2010 D. GalimbertiA. PietroboniG. FumagalliL. GhezziC. FenoglioF. CortiniC. CantoniM. SerpenteN. BresolinE. Scarpini + Article (author) -
CHMP5 and BAG1 are protective factors for sporadic frontotemporal lobar degeneration 2010 D. GalimbertiC. VillaE. VenturelliC. FenoglioD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinC. MarianiE. Scarpini + Article (author) -
Expression profile of miRNAs involved in CD4+ lymphocyte activation and differentiation in patients with multiple sclerosis 2010 D. GalimbertiC. FenoglioD. ScalabriniM. SerpenteC. CantoniM. De RizA. PietroboniM. PiolaE. VenturelliC. VillaF. CortiniN. BresolinE. Scarpini + Article (author) -
Candidate gene analysis of semaphorins in patients with Alzheimer's disease 2010 C. VillaE. VenturelliC. FenoglioM. De RizD. ScalabriniF. CortiniM. SerpenteC. CantoniN. BresolinE. ScarpiniD. Galimberti Article (author) -
GRN Asp22fs mutation is associated with highly variable age at onset, clinical phenotype and brain atrophy 2010 A. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoP. CortiN. BresolinD. GalimbertiE. 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) -
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) -
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred 2011 A.M. PietroboniL. GhezziC. FenoglioF. CortiniM. SerpenteC. CantoniE. RotondoP. CortiN. BresolinD. GalimbertiE.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) -
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) -
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) -
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) -
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) -
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) -
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) -
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) -
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) -
Mostrati risultati da 1 a 20 di 43
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