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[Diagnostic algorithm for autosomal recessive ataxia].
Nuzhnyi EP, Abramycheva NY, Klyushnikov SA, Seliverstov YA, Vetchinova AS, Pogoda TV, Ershova MV, Fedotova EY, Illarioshkin SN. Nuzhnyi EP, et al. Among authors: fedotova ey. Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(9):74-82. doi: 10.17116/jnevro201911909174. Zh Nevrol Psikhiatr Im S S Korsakova. 2019. PMID: 31626222 Russian.
New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
Abramycheva N, Stepanova M, Kalashnikova L, Zakharova M, Maximova M, Tanashyan M, Lagoda O, Fedotova E, Klyushnikov S, Konovalov R, Sakharova A, Illarioshkin S. Abramycheva N, et al. J Neurol Sci. 2015 Feb 15;349(1-2):196-201. doi: 10.1016/j.jns.2015.01.018. Epub 2015 Jan 17. J Neurol Sci. 2015. PMID: 25623805
[Identification of people at the latent stage of Parkinson's disease (the PARKINLAR study): first results and an optimization of the algorithm].
Fedotova EY, Chechetkin AO, Abramycheva NY, Chigaleychik LA, Baziyan BK, Ponomareva ТА, Alexeeva NS, Fedin PA, Kravchenko MA, Varakin YY, Ivanova-Smolenskaya IA, Illarioshkin SN. Fedotova EY, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2015;115(6):4-11. doi: 10.17116/jnevro2015115614-11. Zh Nevrol Psikhiatr Im S S Korsakova. 2015. PMID: 26356391 Russian.
[Functional properties of dopaminergic neurons obtained from fibroblasts of a patient with PARK2 form of Parkinson's disease].
Konovalova ЕV, Ivashkin ЕG, Lopachev АV, Lopacheva ОМ, Komissarov АА, Grivennikov IА, Novosadova ЕV, Dashynimaev EB, Fedotova ЕY, Illarioshkin SN. Konovalova ЕV, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2015;115(12):123-127. doi: 10.17116/jnevro2015115112123-127. Zh Nevrol Psikhiatr Im S S Korsakova. 2015. PMID: 26978505 Russian.
A 30-year history of MPAN case from Russia.
Selikhova M, Fedotova E, Wiethoff S, Schottlaender LV, Klyushnikov S, Illarioshkin SN, Houlden H. Selikhova M, et al. Clin Neurol Neurosurg. 2017 Aug;159:111-113. doi: 10.1016/j.clineuro.2017.05.025. Epub 2017 Jun 2. Clin Neurol Neurosurg. 2017. PMID: 28641177
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.
35 results