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Peter M Andersen

Showing results (61-70 of 241) with videos related to

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Journal of Human Genetics|March 30, 2012
Novel TARDBP mutations in Nordic ALS patientsHuei-Hsin Chiang, Peter M Andersen, Ole-Bjørn Tysnes, et al.
Neurobiology of Aging|June 5, 2018
Frequency of C9orf72 hexanucleotide repeat expansion and SOD1 mutations in Portuguese patients with amyotrophic lateral sclerosisMarta Gromicho, Susana Pinto, Eugeniu Gisca, et al.
Global Qualitative Nursing Research|July 15, 2025
Transformed Parenthood in the Face of ALS: A Profound Struggle for Both Ill Parents and Co-parentsNina Malmström, Joakim Öhlén, Stefan Nilsson, et al.
Social Science & Medicine (1982)|July 6, 2024
Adolescents' challenging and grief-filled transitions when living with a parent with ALS: A qualitative interpretive studyNina Malmström, Joakim Öhlén, Birgitta Jakobsson Larsson, et al.
Acta Neuropathologica Communications|June 23, 2021
Peripheral administration of SOD1 aggregates does not transmit pathogenic aggregation to the CNS of SOD1 transgenic miceIsil Keskin, Elaheh Ekhtiari Bidhendi, Matthew Marklund, et al.
Human Molecular Genetics|August 17, 2010
A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysisAnna Birve, Christoph Neuwirth, Markus Weber, et al.
Brain : a Journal of Neurology|December 7, 2005
Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis modelsP Andreas Jonsson, Karin S Graffmo, Peter M Andersen, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11Bing He, Vilmantas Giedraitis, Arturs Ligers, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 27, 2013
No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and IcelandCaroline Ingre, Susana Pinto, Anna Birve, et al.
Acta Neuropathologica|November 17, 2022
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutationKarin M Forsberg, Karin S Graffmo, Erica Stenvall, et al.
Pageof 25

Showing results (61-70 of 241) with videos related to

Sort By:
Pageof 25
Journal of Human Genetics|March 30, 2012
Novel TARDBP mutations in Nordic ALS patientsHuei-Hsin Chiang, Peter M Andersen, Ole-Bjørn Tysnes, et al.
Neurobiology of Aging|June 5, 2018
Frequency of C9orf72 hexanucleotide repeat expansion and SOD1 mutations in Portuguese patients with amyotrophic lateral sclerosisMarta Gromicho, Susana Pinto, Eugeniu Gisca, et al.
Global Qualitative Nursing Research|July 15, 2025
Transformed Parenthood in the Face of ALS: A Profound Struggle for Both Ill Parents and Co-parentsNina Malmström, Joakim Öhlén, Stefan Nilsson, et al.
Social Science & Medicine (1982)|July 6, 2024
Adolescents' challenging and grief-filled transitions when living with a parent with ALS: A qualitative interpretive studyNina Malmström, Joakim Öhlén, Birgitta Jakobsson Larsson, et al.
Acta Neuropathologica Communications|June 23, 2021
Peripheral administration of SOD1 aggregates does not transmit pathogenic aggregation to the CNS of SOD1 transgenic miceIsil Keskin, Elaheh Ekhtiari Bidhendi, Matthew Marklund, et al.
Human Molecular Genetics|August 17, 2010
A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysisAnna Birve, Christoph Neuwirth, Markus Weber, et al.
Brain : a Journal of Neurology|December 7, 2005
Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis modelsP Andreas Jonsson, Karin S Graffmo, Peter M Andersen, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11Bing He, Vilmantas Giedraitis, Arturs Ligers, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 27, 2013
No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and IcelandCaroline Ingre, Susana Pinto, Anna Birve, et al.
Acta Neuropathologica|November 17, 2022
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutationKarin M Forsberg, Karin S Graffmo, Erica Stenvall, et al.
Pageof 25