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

Jonathan D Glass

Showing results (21-30 of 178) with videos related to

Pageof 18
Sort By:
Neurobiology of Disease|August 29, 2012
Cellular toxicity of mutant SOD1 protein is linked to an easily soluble, non-aggregated form in vitroTerrell E Brotherton, Yingjie Li, Jonathan D Glass
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 8, 2022
Clinically meaningful change: evaluation of the Rasch-built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) and the ALSFRS-RChristina N Fournier, Virginia James, Jonathan D Glass
Neurology|June 4, 2020
Tau deposition in the spinal cord is not specific for CTE-ALSChristina N Fournier, Marla Gearing, Jonathan D Glass
Current Opinion in Neurology|August 7, 2018
Stem cell transplantation for amyotrophic lateral sclerosisRobert H Baloh, Jonathan D Glass, Clive N Svendsen
Experimental Neurology|May 14, 2013
Axonal degeneration in the peripheral nervous system: implications for the pathogenesis of amyotrophic lateral sclerosisLindsey R Fischer-Hayes, Terrell Brotherton, Jonathan D Glass
The Neurohospitalist|August 29, 2013
A 61-year-old woman with progressive weakness and rashEric R Anderson, Jonathan D Glass, James G Greene
Cellular & Molecular Immunology|January 9, 2018
Adoptive transfer of IL-10<sup>+</sup> regulatory B cells decreases myeloid-derived macrophages in the central nervous system in a transgenic amyotrophic lateral sclerosis modelAndrea Pennati, Seneshaw Asress, Jonathan D Glass, et al.
Neurology|December 29, 2020
Comparison of Phenotypic Characteristics and Prognosis Between Black and White Patients in a Tertiary ALS ClinicDavid Brand, Meraida Polak, Jonathan D Glass, et al.
Journal of Molecular Histology|December 23, 2004
Mitochondrial abnormalities in dermatomyositis: characteristic pattern of neuropathologyMohammed I Alhatou, John T Sladky, Omar Bagasra, et al.
The Neurologist|June 14, 2003
A practical approach to the diagnosis and management of MELAS: case report and reviewMadhav Thambisetty, Nancy J Newman, Jonathan D Glass, et al.
Pageof 18

Showing results (21-30 of 178) with videos related to

Sort By:
Pageof 18
Neurobiology of Disease|August 29, 2012
Cellular toxicity of mutant SOD1 protein is linked to an easily soluble, non-aggregated form in vitroTerrell E Brotherton, Yingjie Li, Jonathan D Glass
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 8, 2022
Clinically meaningful change: evaluation of the Rasch-built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) and the ALSFRS-RChristina N Fournier, Virginia James, Jonathan D Glass
Neurology|June 4, 2020
Tau deposition in the spinal cord is not specific for CTE-ALSChristina N Fournier, Marla Gearing, Jonathan D Glass
Current Opinion in Neurology|August 7, 2018
Stem cell transplantation for amyotrophic lateral sclerosisRobert H Baloh, Jonathan D Glass, Clive N Svendsen
Experimental Neurology|May 14, 2013
Axonal degeneration in the peripheral nervous system: implications for the pathogenesis of amyotrophic lateral sclerosisLindsey R Fischer-Hayes, Terrell Brotherton, Jonathan D Glass
The Neurohospitalist|August 29, 2013
A 61-year-old woman with progressive weakness and rashEric R Anderson, Jonathan D Glass, James G Greene
Cellular & Molecular Immunology|January 9, 2018
Adoptive transfer of IL-10<sup>+</sup> regulatory B cells decreases myeloid-derived macrophages in the central nervous system in a transgenic amyotrophic lateral sclerosis modelAndrea Pennati, Seneshaw Asress, Jonathan D Glass, et al.
Neurology|December 29, 2020
Comparison of Phenotypic Characteristics and Prognosis Between Black and White Patients in a Tertiary ALS ClinicDavid Brand, Meraida Polak, Jonathan D Glass, et al.
Journal of Molecular Histology|December 23, 2004
Mitochondrial abnormalities in dermatomyositis: characteristic pattern of neuropathologyMohammed I Alhatou, John T Sladky, Omar Bagasra, et al.
The Neurologist|June 14, 2003
A practical approach to the diagnosis and management of MELAS: case report and reviewMadhav Thambisetty, Nancy J Newman, Jonathan D Glass, et al.
Pageof 18