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

Year Number of Results
2006 2
2008 4
2009 2
2010 2
2011 1
2012 4
2013 5
2014 4
2015 5
2016 8
2017 15
2018 12
2019 3
2020 7
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64 results
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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: tzoulis c. 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.
Glitazone use associated with reduced risk of Parkinson's disease.
Brakedal B, Flønes I, Reiter SF, Torkildsen Ø, Dölle C, Assmus J, Haugarvoll K, Tzoulis C. Brakedal B, et al. Among authors: tzoulis c. Mov Disord. 2017 Nov;32(11):1594-1599. doi: 10.1002/mds.27128. Epub 2017 Sep 1. Mov Disord. 2017. PMID: 28861893 Free PMC article.
Targeting NAD+ in translational research to relieve diseases and conditions of metabolic stress and ageing.
Gilmour BC, Gudmundsrud R, Frank J, Hov A, Lautrup S, Aman Y, Røsjø H, Brenner C, Ziegler M, Tysnes OB, Tzoulis C, Omland T, Søraas A, Holmøy T, Bergersen LH, Storm-Mathisen J, Nilsen H, Fang EF. Gilmour BC, et al. Among authors: tzoulis c. Mech Ageing Dev. 2020 Mar;186:111208. doi: 10.1016/j.mad.2020.111208. Epub 2020 Jan 15. Mech Ageing Dev. 2020. PMID: 31953124 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: tzoulis c. Nat Commun. 2016 Nov 22;7:13548. doi: 10.1038/ncomms13548. Nat Commun. 2016. PMID: 27874000 Free PMC article.
The angiogenic switch leads to a metabolic shift in human glioblastoma.
Talasila KM, Røsland GV, Hagland HR, Eskilsson E, Flønes IH, Fritah S, Azuaje F, Atai N, Harter PN, Mittelbronn M, Andersen M, Joseph JV, Hossain JA, Vallar L, Noorden CJ, Niclou SP, Thorsen F, Tronstad KJ, Tzoulis C, Bjerkvig R, Miletic H. Talasila KM, et al. Among authors: tzoulis c. Neuro Oncol. 2017 Mar 1;19(3):383-393. doi: 10.1093/neuonc/now175. Neuro Oncol. 2017. PMID: 27591677 Free PMC article.
Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients.
Sofou K, de Coo IFM, Ostergaard E, Isohanni P, Naess K, De Meirleir L, Tzoulis C, Uusimaa J, Lönnqvist T, Bindoff LA, Tulinius M, Darin N. Sofou K, et al. Among authors: tzoulis c. J Med Genet. 2018 Jan;55(1):21-27. doi: 10.1136/jmedgenet-2017-104891. Epub 2017 Nov 3. J Med Genet. 2018. PMID: 29101127
[Multiple sclerosis - a mitochondria-mediated disease?].
Varhaug KN, Vedeler CA, Tzoulis C, Bindoff LA. Varhaug KN, et al. Among authors: tzoulis c. 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.
Nigrostriatal denervation sine parkinsonism.
Haugarvoll K, Bindoff LA, Tzoulis C. Haugarvoll K, et al. Among authors: tzoulis c. Brain. 2016 Apr;139(Pt 4):e25. doi: 10.1093/brain/awv410. Epub 2016 Jan 25. Brain. 2016. PMID: 26811251 No abstract available.
Neuronal complex I deficiency occurs throughout the Parkinson's disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage.
Flønes IH, Fernandez-Vizarra E, Lykouri M, Brakedal B, Skeie GO, Miletic H, Lilleng PK, Alves G, Tysnes OB, Haugarvoll K, Dölle C, Zeviani M, Tzoulis C. Flønes IH, et al. Among authors: tzoulis c. Acta Neuropathol. 2018 Mar;135(3):409-425. doi: 10.1007/s00401-017-1794-7. Epub 2017 Dec 21. Acta Neuropathol. 2018. PMID: 29270838
Movement disorders in mitochondrial disease: a clinicopathological correlation.
Flønes IH, Tzoulis C. Flønes IH, et al. Among authors: tzoulis c. Curr Opin Neurol. 2018 Aug;31(4):472-483. doi: 10.1097/WCO.0000000000000583. Curr Opin Neurol. 2018. PMID: 29750731 Review.
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