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

Year Number of Results
2002 4
2003 4
2004 4
2005 1
2006 3
2007 4
2008 9
2009 4
2010 7
2011 12
2012 8
2013 9
2014 5
2015 6
2016 10
2017 13
2018 11
2019 9
2020 16
2021 18
2022 6
2023 9
2024 7
2025 0

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158 results

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Page 1
Mitochondrial disease in adults: recent advances and future promise.
Ng YS, Bindoff LA, Gorman GS, Klopstock T, Kornblum C, Mancuso M, McFarland R, Sue CM, Suomalainen A, Taylor RW, Thorburn DR, Turnbull DM. Ng YS, et al. Lancet Neurol. 2021 Jul;20(7):573-584. doi: 10.1016/S1474-4422(21)00098-3. Lancet Neurol. 2021. PMID: 34146515 Review.
Mitochondrial ataxias.
Vernon HJ, Bindoff LA. Vernon HJ, et al. Handb Clin Neurol. 2018;155:129-141. doi: 10.1016/B978-0-444-64189-2.00009-3. Handb Clin Neurol. 2018. PMID: 29891055 Review.
Felles løft for pasienter med nevromuskulære sykdommer.
Jensen SM, Arntzen KA, Ørstavik K, Rasmussen M, Bindoff LA. Jensen SM, et al. Tidsskr Nor Laegeforen. 2018 Sep 26;138(15). doi: 10.4045/tidsskr.18.0630. Print 2018 Oct 2. Tidsskr Nor Laegeforen. 2018. PMID: 30277043 Free article. Norwegian. No abstract available.
Økt behov for fysioterapeuter med nevromuskulær kompetanse.
Ørstavik K, Rasmussen M, Arntzen KA, Bindoff LA. Ørstavik K, et al. Tidsskr Nor Laegeforen. 2018 Sep 17;138(14). doi: 10.4045/tidsskr.18.0580. Print 2018 Sep 18. Tidsskr Nor Laegeforen. 2018. PMID: 30234257 Free article. Norwegian. No abstract available.
Ataxia in mitochondrial disorders.
Zeviani M, Simonati A, Bindoff LA. Zeviani M, et al. Handb Clin Neurol. 2012;103:359-72. doi: 10.1016/B978-0-444-51892-7.00022-X. Handb Clin Neurol. 2012. PMID: 21827900 Review.
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. Brain. 2024 May 3;147(5):1899-1913. doi: 10.1093/brain/awae018. Brain. 2024. PMID: 38242545 Free PMC article.
[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.
Mitochondrial diseases and epilepsy.
Bindoff LA, Engelsen BA. Bindoff LA, et al. Epilepsia. 2012 Sep;53 Suppl 4:92-7. doi: 10.1111/j.1528-1167.2012.03618.x. Epilepsia. 2012. PMID: 22946726 Free article. Review.
Status epilepticus in POLG disease: a large multinational study.
Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Brodtkorb E, Ostergaard E, de Coo I, Pias-Peleteiro L, Isohanni P, Uusimaa J, Majamaa K, Kärppä M, Ortigoza-Escobar JD, Tangeraas T, Berland S, Harrison E, Biggs H, Horvath R, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. J Neurol. 2024 Aug;271(8):5156-5164. doi: 10.1007/s00415-024-12463-5. Epub 2024 Jun 1. J Neurol. 2024. PMID: 38822839 Free PMC article.
158 results