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

Nereo Bresolin

Showing results (211-220 of 346) with videos related to

Pageof 35
Sort By:
Neurology|August 17, 2014
Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutationDaniela Di Bella, Davide Pareyson, Mario Savoiardo, et al.
Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.
Journal of Neurology|June 15, 2006
Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjectsElisabetta D'Adda, Monica Sciacco, Maria Elisa Fruguglietti, et al.
Neuroscience Letters|September 11, 2007
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosisDiego Scalabrini, Chiara Fenoglio, Elio Scarpini, et al.
Neurobiology of Aging|August 18, 2004
MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levelsChiara Fenoglio, Daniela Galimberti, Carlo Lovati, et al.
Journal of Neurology|June 26, 2008
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegiaRoberta Virgilio, Dario Ronchi, Georgios M Hadjigeorgiou, et al.
Neurobiology of Aging|September 25, 2007
Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?Serena Ghezzi, Roberto Del Bo, Marina Scarlato, et al.
Frontiers in Neurology|February 15, 2021
Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple SclerosisMattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, et al.
Frontiers in Neurology|October 31, 2018
Stormorken Syndrome Caused by a p.R304W <i>STIM1</i> Mutation: The First Italian Patient and a Review of the LiteratureOscar Borsani, Daniela Piga, Stefania Costa, et al.
The Journal of Cell Biology|July 30, 2003
Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy modelYvan Torrente, Geoffrey Camirand, Federica Pisati, et al.
Pageof 35

Showing results (211-220 of 346) with videos related to

Sort By:
Pageof 35
Neurology|August 17, 2014
Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutationDaniela Di Bella, Davide Pareyson, Mario Savoiardo, et al.
Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.
Journal of Neurology|June 15, 2006
Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjectsElisabetta D'Adda, Monica Sciacco, Maria Elisa Fruguglietti, et al.
Neuroscience Letters|September 11, 2007
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosisDiego Scalabrini, Chiara Fenoglio, Elio Scarpini, et al.
Neurobiology of Aging|August 18, 2004
MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levelsChiara Fenoglio, Daniela Galimberti, Carlo Lovati, et al.
Journal of Neurology|June 26, 2008
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegiaRoberta Virgilio, Dario Ronchi, Georgios M Hadjigeorgiou, et al.
Neurobiology of Aging|September 25, 2007
Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?Serena Ghezzi, Roberto Del Bo, Marina Scarlato, et al.
Frontiers in Neurology|February 15, 2021
Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple SclerosisMattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, et al.
Frontiers in Neurology|October 31, 2018
Stormorken Syndrome Caused by a p.R304W <i>STIM1</i> Mutation: The First Italian Patient and a Review of the LiteratureOscar Borsani, Daniela Piga, Stefania Costa, et al.
The Journal of Cell Biology|July 30, 2003
Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy modelYvan Torrente, Geoffrey Camirand, Federica Pisati, et al.
Pageof 35