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SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
Orlén H, Melberg A, Raininko R, Kumlien E, Entesarian M, Söderberg P, Påhlman M, Darin N, Kyllerman M, Holmberg E, Engler H, Eriksson U, Dahl N. Orlén H, et al. Among authors: soderberg p. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):984-92. doi: 10.1002/ajmg.b.30928. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19194956
Assessing the safety of new germicidal far-UVC technologies.
Görlitz M, Justen L, Rochette PJ, Buonanno M, Welch D, Kleiman NJ, Eadie E, Kaidzu S, Bradshaw WJ, Javorsky E, Cridland N, Galor A, Guttmann M, Meinke MC, Schleusener J, Jensen P, Söderberg P, Yamano N, Nishigori C, O'Mahoney P, Manstein D, Croft R, Cole C, de Gruijl FR, Forbes PD, Trokel S, Marshall J, Brenner DJ, Sliney D, Esvelt K. Görlitz M, et al. Among authors: soderberg p. Photochem Photobiol. 2024 May-Jun;100(3):501-520. doi: 10.1111/php.13866. Epub 2023 Nov 6. Photochem Photobiol. 2024. PMID: 37929787 Review.
Evidence for validity of the Swedish self-rated 36-item version of the World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0) in patients with mental disorders: a multi-centre cross-sectional study using Rasch analysis.
Svanborg C, Amer A, Nordenskjöld A, Ramklint M, Söderberg P, Tungström S, Ginsberg Y, Hermansson L. Svanborg C, et al. Among authors: soderberg p. J Patient Rep Outcomes. 2022 May 8;6(1):45. doi: 10.1186/s41687-022-00449-8. J Patient Rep Outcomes. 2022. PMID: 35526195 Free PMC article.
136 results