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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 2
2009 1
2011 2
2012 3
2013 2
2015 2
2016 1
2018 1
2019 2
2020 2
2022 1
2023 2
2024 0

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Page 1
Phenotype in an Infant with SOD1 Homozygous Truncating Mutation.
Andersen PM, Nordström U, Tsiakas K, Johannsen J, Volk AE, Bierhals T, Zetterström P, Marklund SL, Hempel M, Santer R. Andersen PM, et al. Among authors: zetterstrom p. N Engl J Med. 2019 Aug 1;381(5):486-488. doi: 10.1056/NEJMc1905039. Epub 2019 Jul 17. N Engl J Med. 2019. PMID: 31314961 No abstract available.
The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1.
Park JH, Nordström U, Tsiakas K, Keskin I, Elpers C, Mannil M, Heller R, Nolan M, Alburaiky S, Zetterström P, Hempel M, Schara-Schmidt U, Biskup S, Steinacker P, Otto M, Weishaupt J, Hahn A, Santer R, Marquardt T, Marklund SL, Andersen PM. Park JH, et al. Among authors: zetterstrom p. Brain Commun. 2023 Jan 27;5(1):fcad017. doi: 10.1093/braincomms/fcad017. eCollection 2023. Brain Commun. 2023. PMID: 36793789 Free PMC article.
SOD1 aggregation in ALS mice shows simplistic test tube behavior.
Lang L, Zetterström P, Brännström T, Marklund SL, Danielsson J, Oliveberg M. Lang L, et al. Among authors: zetterstrom p. Proc Natl Acad Sci U S A. 2015 Aug 11;112(32):9878-83. doi: 10.1073/pnas.1503328112. Epub 2015 Jul 28. Proc Natl Acad Sci U S A. 2015. PMID: 26221023 Free PMC article.
18 results