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Year Number of Results
2016 1
2017 3
2018 1
2019 2
2020 6
2021 2
2022 3
2023 1

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15 results

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Page 1
[Mitochondrial disease caused by the m.3243A>G mutation].
Varhaug KN, Hikmat O, Bindoff LA. Varhaug KN, et al. Tidsskr Nor Laegeforen. 2022 Jun 27;142(10). doi: 10.4045/tidsskr.21.0729. Print 2022 Jun 28. Tidsskr Nor Laegeforen. 2022. PMID: 35763848 Free article. Review. Norwegian.
[Polymerase gamma-related mitochondrial disorder].
Hikmat O, Varhaug KN, Bindoff LA. Hikmat O, et al. Among authors: varhaug kn. Tidsskr Nor Laegeforen. 2020 Jan 13;140(1). doi: 10.4045/tidsskr.19.0368. Print 2020 Jan 14. Tidsskr Nor Laegeforen. 2020. PMID: 31948198 Free article. Norwegian.
[Multiple sclerosis - a mitochondria-mediated disease?].
Varhaug KN, Vedeler CA, Tzoulis C, Bindoff LA. Varhaug KN, et al. Tidsskr Nor Laegeforen. 2017 Feb 21;137(4):284-287. doi: 10.4045/tidsskr.16.0210. eCollection 2017 Feb. Tidsskr Nor Laegeforen. 2017. PMID: 28225235 Free article. Review. Norwegian.
Serum biomarkers in primary mitochondrial disorders.
Varhaug KN, Hikmat O, Nakkestad HL, Vedeler CA, Bindoff LA. Varhaug KN, et al. Brain Commun. 2021 Jan 4;3(1):fcaa222. doi: 10.1093/braincomms/fcaa222. eCollection 2021. Brain Commun. 2021. PMID: 33501425 Free PMC article.
Research priorities for mitochondrial disorders: Current landscape and patient and professional views.
Thomas RH, Hunter A, Butterworth L, Feeney C, Graves TD, Holmes S, Hossain P, Lowndes J, Sharpe J, Upadhyaya S, Varhaug KN, Votruba M, Wheeler R, Staley K, Rahman S. Thomas RH, et al. Among authors: varhaug kn. J Inherit Metab Dis. 2022 Jul;45(4):796-803. doi: 10.1002/jimd.12521. Epub 2022 May 31. J Inherit Metab Dis. 2022. PMID: 35543492 Free PMC article.
Comment on "A severe linezolid-induced rhabdomyolysis and lactic acidosis in Leigh syndrome".
Bindoff LA, Brown DA, Gorman GS, Karaa A, Keshavan N, Lamperti C, Mancuso M, McFarland R, Ng YS, O'Callaghan M, Pitceathly RDS, Rahman S, Russel FGM, Schirris TJJ, Varhaug KN, De Vries MC. Bindoff LA, et al. Among authors: varhaug kn. J Inherit Metab Dis. 2021 Jan;44(1):6-7. doi: 10.1002/jimd.12329. Epub 2020 Nov 18. J Inherit Metab Dis. 2021. PMID: 33159463 No abstract available.
Using urine to diagnose large-scale mtDNA deletions in adult patients.
Varhaug KN, Nido GS, de Coo I, Isohanni P, Suomalainen A, Tzoulis C, Knappskog P, Bindoff LA. Varhaug KN, et al. Ann Clin Transl Neurol. 2020 Aug;7(8):1318-1326. doi: 10.1002/acn3.51119. Epub 2020 Jul 7. Ann Clin Transl Neurol. 2020. PMID: 32634300 Free PMC article.
Neurofilament light chain predicts disease activity in relapsing-remitting MS.
Varhaug KN, Barro C, Bjørnevik K, Myhr KM, Torkildsen Ø, Wergeland S, Bindoff LA, Kuhle J, Vedeler C. Varhaug KN, et al. Neurol Neuroimmunol Neuroinflamm. 2017 Nov 28;5(1):e422. doi: 10.1212/NXI.0000000000000422. eCollection 2018 Jan. Neurol Neuroimmunol Neuroinflamm. 2017. PMID: 29209636 Free PMC article.
15 results