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

Year Number of Results
2016 1
2017 3
2018 1
2019 2
2020 6
2021 2
2022 3
2023 2
2024 2

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Page 1
Øyesykdom ved dystrophia myotonica type 1.
Boonstra NE, Varhaug KN. Boonstra NE, et al. Among authors: varhaug kn. Tidsskr Nor Laegeforen. 2023 Sep 4;143(13). doi: 10.4045/tidsskr.22.0608. Print 2023 Sep 26. Tidsskr Nor Laegeforen. 2023. PMID: 37753768 Free article. Review. 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.
[Polymerase gamma-related mitochondrial disorder].
Hikmat O, Varhaug KN, Bindoff LA. Hikmat O, et al. 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.
Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation.
Muñoz-Oreja M, Sandoval A, Bruland O, Perez-Rodriguez D, Fernandez-Pelayo U, de Arbina AL, Villar-Fernandez M, Hernández-Eguiazu H, Hernández I, Park Y, Goicoechea L, Pascual-Frías N, Garcia-Ruiz C, Fernandez-Checa J, Martí-Carrera I, Gil-Bea FJ, Hasan MT, Gegg ME, Bredrup C, Knappskog PM, Gereñu-Lopetegui G, Varhaug KN, Bindoff LA, Spinazzola A, Yoon WH, Holt IJ. Muñoz-Oreja M, et al. Among authors: varhaug kn. Brain. 2024 May 3;147(5):1899-1913. doi: 10.1093/brain/awae018. Brain. 2024. PMID: 38242545 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.
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
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.
18 results