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[DNA-based diagnostics of long QT syndrome].
Berge KE, Haugaa KH, Anfinsen OG, Früh A, Hallerud M, Jonsrud C, Øyen N, Gjesdal K, Amlie JP, Leren TP. Berge KE, et al. Among authors: jonsrud c. Tidsskr Nor Laegeforen. 2005 Oct 20;125(20):2783-6. Tidsskr Nor Laegeforen. 2005. PMID: 16244680 Free article. Norwegian.
[A 50-year-old man with proximal pareses and heart disease].
Ørstavik K, Garfelt B, Leren TP, Saberniak J, Haugaa K, Jonsrud C. Ørstavik K, et al. Among authors: jonsrud c. Tidsskr Nor Laegeforen. 2017 Sep 4;137(16). doi: 10.4045/tidsskr.16.0789. Print 2017 Sep 5. Tidsskr Nor Laegeforen. 2017. PMID: 28871726 Free article. Norwegian. No abstract available.
A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene.
Løseth S, Voermans NC, Torbergsen T, Lillis S, Jonsrud C, Lindal S, Kamsteeg EJ, Lammens M, Broman M, Dekomien G, Maddison P, Muntoni F, Sewry C, Radunovic A, de Visser M, Straub V, van Engelen B, Jungbluth H. Løseth S, et al. Among authors: jonsrud c. J Neurol. 2013 Jun;260(6):1504-10. doi: 10.1007/s00415-012-6817-7. Epub 2013 Jan 18. J Neurol. 2013. PMID: 23329375
20 results