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

Year Number of Results
2016 1
2017 1
2018 5
2019 1
2022 2
2023 3
2024 1

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12 results

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Page 1
Mitochondrial diseases caused by mtDNA mutations: a mini-review.
Ryzhkova AI, Sazonova MA, Sinyov VV, Galitsyna EV, Chicheva MM, Melnichenko AA, Grechko AV, Postnov AY, Orekhov AN, Shkurat TP. Ryzhkova AI, et al. Among authors: shkurat tp. Ther Clin Risk Manag. 2018 Oct 9;14:1933-1942. doi: 10.2147/TCRM.S154863. eCollection 2018. Ther Clin Risk Manag. 2018. PMID: 30349272 Free PMC article. Review.
Mitochondrial genome sequencing in atherosclerosis: what's next?
Sazonova MA, Shkurat TP, Demakova NA, Zhelankin AV, Barinova VA, Sobenin IA, Orekhov AN. Sazonova MA, et al. Among authors: shkurat tp. Curr Pharm Des. 2016;22(3):390-6. doi: 10.2174/1381612822666151112152335. Curr Pharm Des. 2016. PMID: 26561059 Review.
Mitochondrial Genome Mutations Associated with Myocardial Infarction.
Sazonova MA, Ryzhkova AI, Sinyov VV, Galitsyna EV, Melnichenko AA, Demakova NA, Sobenin IA, Shkurat TP, Orekhov AN. Sazonova MA, et al. Among authors: shkurat tp. Dis Markers. 2018 Feb 18;2018:9749457. doi: 10.1155/2018/9749457. eCollection 2018. Dis Markers. 2018. PMID: 29670672 Free PMC article.
Response to: Comment on "Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis".
Sobenin IA, Sazonova MA, Sinyov VV, Ryzhkova AI, Galitsyna EV, Khasanova ZB, Postnov AY, Yarygina EI, Shkurat TP, Orekhov AN. Sobenin IA, et al. Among authors: shkurat tp. Oxid Med Cell Longev. 2018 Aug 9;2018:7620234. doi: 10.1155/2018/7620234. eCollection 2018. Oxid Med Cell Longev. 2018. PMID: 30159117 Free PMC article. No abstract available.
12 results