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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 10
2019 9
2020 9
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Search Results

116 results
Results by year
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Page 1
Understanding the Epilepsy in POLG Related Disease.
Hikmat O, Eichele T, Tzoulis C, Bindoff LA. Hikmat O, et al. Among authors: Bindoff LA. Int J Mol Sci. 2017 Aug 24;18(9):1845. doi: 10.3390/ijms18091845. Int J Mol Sci. 2017. PMID: 28837072 Free PMC article. Review.
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration.
Brunetti D, Torsvik J, Dallabona C, Teixeira P, Sztromwasser P, Fernandez-Vizarra E, Cerutti R, Reyes A, Preziuso C, D'Amati G, Baruffini E, Goffrini P, Viscomi C, Ferrero I, Boman H, Telstad W, Johansson S, Glaser E, Knappskog PM, Zeviani M, Bindoff LA. Brunetti D, et al. Among authors: Bindoff LA. EMBO Mol Med. 2016 Mar 1;8(3):176-90. doi: 10.15252/emmm.201505894. EMBO Mol Med. 2016. PMID: 26697887 Free PMC article.
Mitochondrial ataxias.
Vernon HJ, Bindoff LA. Vernon HJ, et al. Among authors: Bindoff LA. Handb Clin Neurol. 2018;155:129-141. doi: 10.1016/B978-0-444-64189-2.00009-3. Handb Clin Neurol. 2018. PMID: 29891055 Review.
Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease.
Dölle C, Flønes I, Nido GS, Miletic H, Osuagwu N, Kristoffersen S, Lilleng PK, Larsen JP, Tysnes OB, Haugarvoll K, Bindoff LA, Tzoulis C. Dölle C, et al. Among authors: Bindoff LA. Nat Commun. 2016 Nov 22;7:13548. doi: 10.1038/ncomms13548. Nat Commun. 2016. PMID: 27874000 Free PMC article.
Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy.
Sommerville EW, Ng YS, Alston CL, Dallabona C, Gilberti M, He L, Knowles C, Chin SL, Schaefer AM, Falkous G, Murdoch D, Longman C, de Visser M, Bindoff LA, Rawles JM, Dean JCS, Petty RK, Farrugia ME, Haack TB, Prokisch H, McFarland R, Turnbull DM, Donnini C, Taylor RW, Gorman GS. Sommerville EW, et al. Among authors: Bindoff LA. JAMA Neurol. 2017 Jun 1;74(6):686-694. doi: 10.1001/jamaneurol.2016.4357. JAMA Neurol. 2017. PMID: 28395030 Free PMC article. Clinical Trial.
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.
Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman JW, Bindoff LA, Rahman S. Hikmat O, et al. Among authors: Bindoff LA. Genet Med. 2017 Nov;19(11):1217-1225. doi: 10.1038/gim.2017.35. Epub 2017 Apr 27. Genet Med. 2017. PMID: 28471437 Clinical Trial.
[Multiple sclerosis - a mitochondria-mediated disease?].
Varhaug KN, Vedeler CA, Tzoulis C, Bindoff LA. Varhaug KN, et al. Among authors: Bindoff LA. 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.
Felles løft for pasienter med nevromuskulære sykdommer.
Jensen SM, Arntzen KA, Ørstavik K, Rasmussen M, Bindoff LA. Jensen SM, et al. Among authors: Bindoff LA. 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. Among authors: Bindoff LA. 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.
Nigrostriatal denervation sine parkinsonism.
Haugarvoll K, Bindoff LA, Tzoulis C. Haugarvoll K, et al. Among authors: Bindoff LA. Brain. 2016 Apr;139(Pt 4):e25. doi: 10.1093/brain/awv410. Epub 2016 Jan 25. Brain. 2016. PMID: 26811251 No abstract available.
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