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Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group.
Mancuso M, Papadopoulou MT, Ng YS, Ardissone A, Bellusci M, Bertini E, Di Vito L, Evangelista T, Fons C, Hikmat O, Horvath R, Klopstock T, Kornblum C, Lamperti C, Licchetta L, Molnar MJ, Varhaug KN, O'Callaghan M, Pressler RM, Schiff M, Servidei S, Szabo N, Gorman GS, Cross JH, Rahman S. Mancuso M, et al. Among authors: varhaug kn. Eur J Neurol. 2024 Apr 4:e16275. doi: 10.1111/ene.16275. Online ahead of print. Eur J Neurol. 2024. PMID: 38576261
Safety of drug use in patients with a primary mitochondrial disease: An international Delphi-based consensus.
De Vries MC, Brown DA, Allen ME, Bindoff L, Gorman GS, Karaa A, Keshavan N, Lamperti C, McFarland R, Ng YS, O'Callaghan M, Pitceathly RDS, Rahman S, Russel FGM, Varhaug KN, Schirris TJJ, Mancuso M. De Vries MC, et al. Among authors: varhaug kn. J Inherit Metab Dis. 2020 Jul;43(4):800-818. doi: 10.1002/jimd.12196. Epub 2020 Feb 7. J Inherit Metab Dis. 2020. PMID: 32030781 Free PMC article.
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.
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.
[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.
[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.
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.
20 results