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

Peter M Andersen

Showing results (101-110 of 241) with videos related to

Pageof 25
Sort By:
Plos One|February 27, 2016
Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS PatientsIsil Keskin, Elin Forsgren, Dale J Lange, et al.
Neurobiology of Disease|November 3, 2024
Specific analysis of SOD1 enzymatic activity in CSF from ALS patients with and without SOD1 mutationsLaura Leykam, Karin M E Forsberg, Ulrika Nordström, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 14, 2009
Aggressive familial ALS with unusual brain MRI and a SOD1 gene mutationSergiu C Blumen, Rivka Inzelberg, Puiu Nisipeanu, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 23, 2007
Volumetric cortical loss in sporadic and familial amyotrophic lateral sclerosisMartin R Turner, Alexander Hammers, Joanna Allsop, et al.
The New England Journal of Medicine|July 18, 2019
Phenotype in an Infant with <i>SOD1</i> Homozygous Truncating MutationPeter M Andersen, Ulrika Nordström, Konstantinos Tsiakas, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS modelsPer Zetterström, Heather G Stewart, Daniel Bergemalm, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?Ansgar Felbecker, William Camu, Paul N Valdmanis, et al.
Plos One|July 21, 2010
Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patientsKarin Forsberg, P Andreas Jonsson, Peter M Andersen, et al.
European Journal of Neurology|March 7, 2022
Respiratory onset of amyotrophic lateral sclerosis in a pregnant woman with a novel SOD1 mutationPegah Masrori, Simona Ospitalieri, Karin Forsberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 25, 2015
Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mappingJohan Bergh, Per Zetterström, Peter M Andersen, et al.
Pageof 25

Showing results (101-110 of 241) with videos related to

Sort By:
Pageof 25
Plos One|February 27, 2016
Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS PatientsIsil Keskin, Elin Forsgren, Dale J Lange, et al.
Neurobiology of Disease|November 3, 2024
Specific analysis of SOD1 enzymatic activity in CSF from ALS patients with and without SOD1 mutationsLaura Leykam, Karin M E Forsberg, Ulrika Nordström, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 14, 2009
Aggressive familial ALS with unusual brain MRI and a SOD1 gene mutationSergiu C Blumen, Rivka Inzelberg, Puiu Nisipeanu, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 23, 2007
Volumetric cortical loss in sporadic and familial amyotrophic lateral sclerosisMartin R Turner, Alexander Hammers, Joanna Allsop, et al.
The New England Journal of Medicine|July 18, 2019
Phenotype in an Infant with <i>SOD1</i> Homozygous Truncating MutationPeter M Andersen, Ulrika Nordström, Konstantinos Tsiakas, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS modelsPer Zetterström, Heather G Stewart, Daniel Bergemalm, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?Ansgar Felbecker, William Camu, Paul N Valdmanis, et al.
Plos One|July 21, 2010
Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patientsKarin Forsberg, P Andreas Jonsson, Peter M Andersen, et al.
European Journal of Neurology|March 7, 2022
Respiratory onset of amyotrophic lateral sclerosis in a pregnant woman with a novel SOD1 mutationPegah Masrori, Simona Ospitalieri, Karin Forsberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 25, 2015
Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mappingJohan Bergh, Per Zetterström, Peter M Andersen, et al.
Pageof 25