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Page 1
Parkinson's Disease: Available Clinical and Promising Omics Tests for Diagnostics, Disease Risk Assessment, and Pharmacotherapy Personalization.
Diagnostics (Basel). 2020 May 25;10(5):339. doi: 10.3390/diagnostics10050339.
Diagnostics (Basel). 2020.
PMID: 32466249
Free PMC article.
Review.
Anomia: Deciphering Functional Neuroanatomy in Primary Progressive Aphasia Variants.
Akhmadullina DR, Konovalov RN, Shpilyukova YA, Fedotova EY, Illarioshkin SN.
Akhmadullina DR, et al. Among authors: fedotova ey.
Brain Sci. 2023 Dec 11;13(12):1703. doi: 10.3390/brainsci13121703.
Brain Sci. 2023.
PMID: 38137151
Free PMC article.
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SNCA Gene Methylation in Parkinson's Disease and Multiple System Atrophy.
Fedotova EY, Iakovenko EV, Abramycheva NY, Illarioshkin SN.
Fedotova EY, et al.
Epigenomes. 2023 Feb 6;7(1):5. doi: 10.3390/epigenomes7010005.
Epigenomes. 2023.
PMID: 36810559
Free PMC article.
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Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson's Disease.
Shulskaya MV, Alieva AK, Vlasov IN, Zyrin VV, Fedotova EY, Abramycheva NY, Usenko TS, Yakimovsky AF, Emelyanov AK, Pchelina SN, Illarioshkin SN, Slominsky PA, Shadrina MI.
Shulskaya MV, et al. Among authors: fedotova ey.
Front Aging Neurosci. 2018 May 15;10:136. doi: 10.3389/fnagi.2018.00136. eCollection 2018.
Front Aging Neurosci. 2018.
PMID: 29867446
Free PMC article.
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Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.
Shulskaya MV, Shadrina MI, Fedotova EY, Abramycheva NY, Limborska SA, Illarioshkin SN, Slominsky PA.
Shulskaya MV, et al. Among authors: fedotova ey.
Int J Neurosci. 2017 Sep;127(9):781-784. doi: 10.1080/00207454.2016.1255612. Epub 2016 Nov 16.
Int J Neurosci. 2017.
PMID: 27798970
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