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

Year Number of Results
2002 1
2003 1
2004 2
2007 1
2008 1
2009 1
2010 2
2012 4
2014 3
2015 3
2017 3
2018 6
2019 5
2020 6
2021 1
2023 3
2024 0

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37 results

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Page 1
Mitochondrial Genome Variation in Polish Elite Athletes.
Piotrowska-Nowak A, Safranow K, Adamczyk JG, Sołtyszewski I, Cięszczyk P, Tońska K, Żekanowski C, Borzemska B. Piotrowska-Nowak A, et al. Among authors: tonska k. Int J Mol Sci. 2023 Aug 20;24(16):12992. doi: 10.3390/ijms241612992. Int J Mol Sci. 2023. PMID: 37629173 Free PMC article.
To Be a Champion of the 24-h Ultramarathon Race. If Not the Heart ... Mosaic Theory?
Gajda R, Samełko A, Czuba M, Piotrowska-Nowak A, Tońska K, Żekanowski C, Klisiewicz A, Drygas W, Gębska-Kuczerowska A, Gajda J, Knechtle B, Adamczyk JG. Gajda R, et al. Among authors: tonska k. Int J Environ Res Public Health. 2021 Mar 1;18(5):2371. doi: 10.3390/ijerph18052371. Int J Environ Res Public Health. 2021. PMID: 33804352 Free PMC article.
Answer to Finsterer about "Multisystem presentation of a homozygous POLG2 variant".
Dosekova P, Dubiel A, Karlowicz A, Zietkiewicz S, Rydzanicz M, Habalova V, Pienkowski VM, Skirkova M, Han V, Mosejova A, Gdovinova Z, Kaliszewska M, Tońska K, Szymanski MR, Skorvanek M, Ploski R. Dosekova P, et al. Among authors: tonska k. Eur J Med Genet. 2020 May;63(5):103900. doi: 10.1016/j.ejmg.2020.103900. Epub 2020 Mar 9. Eur J Med Genet. 2020. PMID: 32165262 No abstract available.
Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion.
Dosekova P, Dubiel A, Karlowicz A, Zietkiewicz S, Rydzanicz M, Habalova V, Pienkowski VM, Skirkova M, Han V, Mosejova A, Gdovinova Z, Kaliszewska M, Tońska K, Szymanski MR, Skorvanek M, Ploski R. Dosekova P, et al. Among authors: tonska k. Eur J Med Genet. 2020 Apr;63(4):103821. doi: 10.1016/j.ejmg.2019.103821. Epub 2019 Nov 26. Eur J Med Genet. 2020. PMID: 31778857
37 results