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E Scarpini

Showing results (91-100 of 110) with videos related to

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European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Clinical Genetics|June 1, 2011
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2C Crimella, C Baschirotto, A Arnoldi, et al.
Neuro-Degenerative Diseases|January 21, 2012
Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's diseaseB Arosio, A Bulbarelli, S Bastias Candia, et al.
Geroscience|February 1, 2023
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effectC Visconte, M T Golia, C Fenoglio, et al.
Current Alzheimer Research|August 20, 2013
CHF5074 Reduces Biomarkers of Neuroinflammation in Patients with Mild Cognitive Impairment: A 12-Week, Double-Blind, Placebo-Controlled StudyJ Ross, S Sharma, J Winston, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 7, 2008
The results of two multicenter, open-label studies assessing efficacy, tolerability and safety of protiramer, a high molecular weight synthetic copolymeric mixture, in patients with relapsing-remitting multiple sclerosisN De Stefano, M Filippi, C Confavreux, et al.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology|January 14, 2010
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohortF Martinelli-Boneschi, F Esposito, D Scalabrini, et al.
European Journal of Neurology|May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degenerationC Villa, E Venturelli, C Fenoglio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in ItalyB Borroni, R Turrone, D Galimberti, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Clinical Genetics|June 1, 2011
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2C Crimella, C Baschirotto, A Arnoldi, et al.
Neuro-Degenerative Diseases|January 21, 2012
Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's diseaseB Arosio, A Bulbarelli, S Bastias Candia, et al.
Geroscience|February 1, 2023
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effectC Visconte, M T Golia, C Fenoglio, et al.
Current Alzheimer Research|August 20, 2013
CHF5074 Reduces Biomarkers of Neuroinflammation in Patients with Mild Cognitive Impairment: A 12-Week, Double-Blind, Placebo-Controlled StudyJ Ross, S Sharma, J Winston, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 7, 2008
The results of two multicenter, open-label studies assessing efficacy, tolerability and safety of protiramer, a high molecular weight synthetic copolymeric mixture, in patients with relapsing-remitting multiple sclerosisN De Stefano, M Filippi, C Confavreux, et al.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology|January 14, 2010
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohortF Martinelli-Boneschi, F Esposito, D Scalabrini, et al.
European Journal of Neurology|May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degenerationC Villa, E Venturelli, C Fenoglio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in ItalyB Borroni, R Turrone, D Galimberti, et al.
Pageof 11