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

Stefania Corti

Showing results (171-180 of 287) with videos related to

Pageof 29
Sort By:
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, 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|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.
Frontiers in Psychology|November 4, 2015
Chronic care management of globesity: promoting healthier lifestyles in traditional and mHealth based settingsGianluca Castelnuovo, Giada Pietrabissa, Gian Mauro Manzoni, et al.
Annals of Neurology|May 16, 2007
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis miceFederica Locatelli, Stefania Corti, Dimitra Papadimitriou, et al.
Journal of the Neurological Sciences|December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian familiesMichela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|August 27, 2009
Association study between XRCC1 gene polymorphisms and sporadic amyotrophic lateral sclerosisFabio Coppedè, Francesca Migheli, Annalisa Lo Gerfo, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
Parkinsonism & Related Disorders|July 3, 2021
Screening of LRP10 mutations in Parkinson's disease patients from ItalyArianna Manini, Letizia Straniero, Edoardo Monfrini, et al.
Brain : a Journal of Neurology|April 19, 2023
Regional spreading pattern is associated with clinical phenotype in amyotrophic lateral sclerosisAlessio Maranzano, Federico Verde, Eleonora Colombo, et al.
Pageof 29

Showing results (171-180 of 287) with videos related to

Sort By:
Pageof 29
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, 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|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.
Frontiers in Psychology|November 4, 2015
Chronic care management of globesity: promoting healthier lifestyles in traditional and mHealth based settingsGianluca Castelnuovo, Giada Pietrabissa, Gian Mauro Manzoni, et al.
Annals of Neurology|May 16, 2007
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis miceFederica Locatelli, Stefania Corti, Dimitra Papadimitriou, et al.
Journal of the Neurological Sciences|December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian familiesMichela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|August 27, 2009
Association study between XRCC1 gene polymorphisms and sporadic amyotrophic lateral sclerosisFabio Coppedè, Francesca Migheli, Annalisa Lo Gerfo, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
Parkinsonism & Related Disorders|July 3, 2021
Screening of LRP10 mutations in Parkinson's disease patients from ItalyArianna Manini, Letizia Straniero, Edoardo Monfrini, et al.
Brain : a Journal of Neurology|April 19, 2023
Regional spreading pattern is associated with clinical phenotype in amyotrophic lateral sclerosisAlessio Maranzano, Federico Verde, Eleonora Colombo, et al.
Pageof 29