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Peter M Andersen

Showing results (71-80 of 241) with videos related to

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Scientific Reports|January 8, 2022
SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severityMariusz Berdyński, Przemysław Miszta, Krzysztof Safranow, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 21, 2006
Overloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis modelsDaniel Bergemalm, P Andreas Jonsson, Karin S Graffmo, et al.
Journal of Neurology|January 9, 2026
Heterogeneous phenotype and cardiovascular comorbidities in Swedish patients with spinobulbar muscular atrophyAnna-Karin Roos, Simon Forsberg, Erica Stenvall, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2016
Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic riskRicarda A L Menke, Malcolm Proudfoot, Joanne Wuu, et al.
Brain : a Journal of Neurology|May 20, 2022
Mild motor impairment as prodromal state in amyotrophic lateral sclerosis: a new diagnostic entityMichael Benatar, Volkan Granit, Peter M Andersen, et al.
Journal of Molecular Neuroscience : MN|November 14, 2019
Targeted Multiple Reaction Monitoring Analysis of CSF Identifies UCHL1 and GPNMB as Candidate Biomarkers for ALSShaochun Zhu, Anna Wuolikainen, Junfang Wu, et al.
Frontiers in Cellular Neuroscience|November 26, 2024
Upregulated miR-10b-5p as a potential miRNA signature in amyotrophic lateral sclerosis patientsBanaja P Dash, Axel Freischmidt, Anika M Helferich, et al.
Journal of Neurochemistry|April 24, 2010
Superoxide dismutase-1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model miceDaniel Bergemalm, Karin Forsberg, Vaibhav Srivastava, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2013
Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosisPetra Bergström, Malin von Otter, Staffan Nilsson, et al.
Acta Neuropathologica|October 5, 2018
Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosisElaheh Ekhtiari Bidhendi, Johan Bergh, Per Zetterström, et al.
Pageof 25

Showing results (71-80 of 241) with videos related to

Sort By:
Pageof 25
Scientific Reports|January 8, 2022
SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severityMariusz Berdyński, Przemysław Miszta, Krzysztof Safranow, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 21, 2006
Overloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis modelsDaniel Bergemalm, P Andreas Jonsson, Karin S Graffmo, et al.
Journal of Neurology|January 9, 2026
Heterogeneous phenotype and cardiovascular comorbidities in Swedish patients with spinobulbar muscular atrophyAnna-Karin Roos, Simon Forsberg, Erica Stenvall, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2016
Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic riskRicarda A L Menke, Malcolm Proudfoot, Joanne Wuu, et al.
Brain : a Journal of Neurology|May 20, 2022
Mild motor impairment as prodromal state in amyotrophic lateral sclerosis: a new diagnostic entityMichael Benatar, Volkan Granit, Peter M Andersen, et al.
Journal of Molecular Neuroscience : MN|November 14, 2019
Targeted Multiple Reaction Monitoring Analysis of CSF Identifies UCHL1 and GPNMB as Candidate Biomarkers for ALSShaochun Zhu, Anna Wuolikainen, Junfang Wu, et al.
Frontiers in Cellular Neuroscience|November 26, 2024
Upregulated miR-10b-5p as a potential miRNA signature in amyotrophic lateral sclerosis patientsBanaja P Dash, Axel Freischmidt, Anika M Helferich, et al.
Journal of Neurochemistry|April 24, 2010
Superoxide dismutase-1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model miceDaniel Bergemalm, Karin Forsberg, Vaibhav Srivastava, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2013
Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosisPetra Bergström, Malin von Otter, Staffan Nilsson, et al.
Acta Neuropathologica|October 5, 2018
Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosisElaheh Ekhtiari Bidhendi, Johan Bergh, Per Zetterström, et al.
Pageof 25