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Peter M Andersen

Showing results (161-170 of 241) with videos related to

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Brain : a Journal of Neurology|December 11, 2025
Somatic gene mutations in the motor cortex of patients with sporadic amyotrophic lateral sclerosisÓscar González-Velasco, Rosanna Parlato, Rüstem Yilmaz, et al.
Annals of Neurology|May 9, 2017
Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutationsDale J Lange, Mona Shahbazi, Vincenzo Silani, et al.
Neuron|July 6, 2004
Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondriaJian Liu, Concepción Lillo, P Andreas Jonsson, et al.
Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.
Brain : a Journal of Neurology|September 7, 2014
Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriersAxel Freischmidt, Kathrin Müller, Lisa Zondler, et al.
American Journal of Human Genetics|September 16, 2025
Landscapes of missense variant impact for human superoxide dismutase 1Anna Axakova, Megan Ding, Atina G Cote, et al.
Biorxiv : the Preprint Server for Biology|March 10, 2025
Landscapes of missense variant impact for human superoxide dismutase 1Anna Axakova, Megan Ding, Atina G Cote, et al.
Human Mutation|April 10, 2013
A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALSHélène Blasco, Nathalie Bernard-Marissal, Patrick Vourc'h, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 30, 2021
Caregivers' divergent perspectives on patients' well-being and attitudes towards hastened death in Germany, Poland and SwedenPeter M Andersen, Magdalena Kuźma-Kozakiewicz, Jürgen Keller, et al.
Brain Communications|February 16, 2023
The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1Julien H Park, Ulrika Nordström, Konstantinos Tsiakas, et al.
Pageof 25

Showing results (161-170 of 241) with videos related to

Sort By:
Pageof 25
Brain : a Journal of Neurology|December 11, 2025
Somatic gene mutations in the motor cortex of patients with sporadic amyotrophic lateral sclerosisÓscar González-Velasco, Rosanna Parlato, Rüstem Yilmaz, et al.
Annals of Neurology|May 9, 2017
Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutationsDale J Lange, Mona Shahbazi, Vincenzo Silani, et al.
Neuron|July 6, 2004
Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondriaJian Liu, Concepción Lillo, P Andreas Jonsson, et al.
Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.
Brain : a Journal of Neurology|September 7, 2014
Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriersAxel Freischmidt, Kathrin Müller, Lisa Zondler, et al.
American Journal of Human Genetics|September 16, 2025
Landscapes of missense variant impact for human superoxide dismutase 1Anna Axakova, Megan Ding, Atina G Cote, et al.
Biorxiv : the Preprint Server for Biology|March 10, 2025
Landscapes of missense variant impact for human superoxide dismutase 1Anna Axakova, Megan Ding, Atina G Cote, et al.
Human Mutation|April 10, 2013
A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALSHélène Blasco, Nathalie Bernard-Marissal, Patrick Vourc'h, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 30, 2021
Caregivers' divergent perspectives on patients' well-being and attitudes towards hastened death in Germany, Poland and SwedenPeter M Andersen, Magdalena Kuźma-Kozakiewicz, Jürgen Keller, et al.
Brain Communications|February 16, 2023
The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1Julien H Park, Ulrika Nordström, Konstantinos Tsiakas, et al.
Pageof 25