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

Year Number of Results
2004 5
2005 4
2006 4
2007 3
2008 4
2009 4
2010 3
2012 2
2013 1
2014 3
2015 3
2016 4
2017 4
2018 6
2019 1
2020 8
2021 9
2022 0
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58 results
Results by year
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Page 1
Inflammation in ALS and SMA: sorting out the good from the evil.
Papadimitriou D, Le Verche V, Jacquier A, Ikiz B, Przedborski S, Re DB. Papadimitriou D, et al. Neurobiol Dis. 2010 Mar;37(3):493-502. doi: 10.1016/j.nbd.2009.10.005. Epub 2009 Oct 13. Neurobiol Dis. 2010. PMID: 19833209 Free PMC article. Review.
Pathophysiology of bone loss in the female athlete.
Lambrinoudaki I, Papadimitriou D. Lambrinoudaki I, et al. Among authors: papadimitriou d. Ann N Y Acad Sci. 2010 Sep;1205:45-50. doi: 10.1111/j.1749-6632.2010.05681.x. Ann N Y Acad Sci. 2010. PMID: 20840252 Review.
CYP1A2 rs762551 polymorphism and risk for amyotrophic lateral sclerosis.
Siokas V, Karampinis E, Aloizou AM, Mentis AA, Liakos P, Papadimitriou D, Liampas I, Nasios G, Bogdanos DP, Hadjigeorgiou GM, Dardiotis E. Siokas V, et al. Among authors: papadimitriou d. Neurol Sci. 2021 Jan;42(1):175-182. doi: 10.1007/s10072-020-04535-x. Epub 2020 Jun 26. Neurol Sci. 2021. PMID: 32592103
Apathy: An underestimated feature in GBA and LRRK2 non-manifesting mutation carriers.
Pachi I, Koros C, Simitsi AM, Papadimitriou D, Bougea A, Prentakis A, Papagiannakis N, Bozi M, Antonelou R, Angelopoulou E, Beratis I, Stamelou M, Trapali XG, Papageorgiou SG, Stefanis L. Pachi I, et al. Among authors: papadimitriou d. Parkinsonism Relat Disord. 2021 Oct;91:1-8. doi: 10.1016/j.parkreldis.2021.08.008. Epub 2021 Aug 18. Parkinsonism Relat Disord. 2021. PMID: 34425330
Serum Uric Acid in LRRK2 Related Parkinson's Disease: Longitudinal Data from the PPMI Study.
Bougea A, Koros C, Papagiannakis N, Simitsi AM, Prentakis A, Papadimitriou D, Pachi I, Antonelou R, Angelopoulou E, Beratis I, Bozi M, Papageorgiou SG, Trapali XG, Stamelou M, Stefanis L. Bougea A, et al. Among authors: papadimitriou d. J Parkinsons Dis. 2021;11(2):633-640. doi: 10.3233/JPD-202337. J Parkinsons Dis. 2021. PMID: 33682725
A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature.
Dardiotis E, Siokas V, Pantazi E, Dardioti M, Rikos D, Xiromerisiou G, Markou A, Papadimitriou D, Speletas M, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: papadimitriou d. Neurobiol Aging. 2017 May;53:194.e13-194.e22. doi: 10.1016/j.neurobiolaging.2017.01.015. Epub 2017 Jan 20. Neurobiol Aging. 2017. PMID: 28214109 Review.
58 results