Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Scarpini

Showing results (81-90 of 110) with videos related to

Pageof 11
Sort By:
European Journal of Neurology|January 26, 2007
CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical courseD Galimberti, D Scalabrini, C Fenoglio, et al.
Acta Neurologica Scandinavica|September 3, 2010
Clinical features of Sjogren's syndrome in patients with multiple sclerosisP Annunziata, L De Santi, S Di Rezze, et al.
The Journal of Endocrinology|October 16, 2002
Plasma ghrelin concentrations in elderly subjects: comparison with anorexic and obese patientsA E Rigamonti, A I Pincelli, B Corrà, et al.
Brain Research|February 9, 1988
Cultures of human Schwann cells isolated from fetal nervesE Scarpini, B Q Kreider, R P Lisak, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2008
MDC/CCL22 intrathecal levels in patients with multiple sclerosisD Galimberti, C Fenoglio, C Comi, et al.
Brain, Behavior, and Immunity|May 30, 2015
Inflammatory molecules in Frontotemporal Dementia: cerebrospinal fluid signature of progranulin mutation carriersD Galimberti, R Bonsi, C Fenoglio, et al.
European Journal of Neurology|September 7, 2020
Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutationM Scarioni, A Arighi, C Fenoglio, et al.
Rejuvenation Research|August 30, 2008
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degenerationB Borroni, S Ghezzi, C Agosti, et al.
Cytokine|January 29, 2019
Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola DiseaseD Galimberti, C Fenoglio, L Ghezzi, et al.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
Pageof 11

Showing results (81-90 of 110) with videos related to

Sort By:
Pageof 11
European Journal of Neurology|January 26, 2007
CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical courseD Galimberti, D Scalabrini, C Fenoglio, et al.
Acta Neurologica Scandinavica|September 3, 2010
Clinical features of Sjogren's syndrome in patients with multiple sclerosisP Annunziata, L De Santi, S Di Rezze, et al.
The Journal of Endocrinology|October 16, 2002
Plasma ghrelin concentrations in elderly subjects: comparison with anorexic and obese patientsA E Rigamonti, A I Pincelli, B Corrà, et al.
Brain Research|February 9, 1988
Cultures of human Schwann cells isolated from fetal nervesE Scarpini, B Q Kreider, R P Lisak, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2008
MDC/CCL22 intrathecal levels in patients with multiple sclerosisD Galimberti, C Fenoglio, C Comi, et al.
Brain, Behavior, and Immunity|May 30, 2015
Inflammatory molecules in Frontotemporal Dementia: cerebrospinal fluid signature of progranulin mutation carriersD Galimberti, R Bonsi, C Fenoglio, et al.
European Journal of Neurology|September 7, 2020
Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutationM Scarioni, A Arighi, C Fenoglio, et al.
Rejuvenation Research|August 30, 2008
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degenerationB Borroni, S Ghezzi, C Agosti, et al.
Cytokine|January 29, 2019
Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola DiseaseD Galimberti, C Fenoglio, L Ghezzi, et al.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
Pageof 11