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Page 1
Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson's Disease.
Int J Mol Sci. 2023 May 22;24(10):9105. doi: 10.3390/ijms24109105.
Int J Mol Sci. 2023.
PMID: 37240451
Free PMC article.
Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?
Kopytova AE, Usenko TS, Baydakova GV, Nikolaev MA, Senkevich KA, Izyumchenko AD, Tyurin AA, Miliukhina IV, Emelyanov AK, Zakharova EY, Pchelina SN.
Kopytova AE, et al. Among authors: miliukhina iv.
Mov Disord. 2022 Aug;37(8):1779-1781. doi: 10.1002/mds.29132. Epub 2022 Jul 6.
Mov Disord. 2022.
PMID: 35792565
No abstract available.
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Mutation analysis of Parkinson's disease genes in a Russian data set.
Emelyanov AK, Usenko TS, Tesson C, Senkevich KA, Nikolaev MA, Miliukhina IV, Kopytova AE, Timofeeva AA, Yakimovsky AF, Lesage S, Brice A, Pchelina SN.
Emelyanov AK, et al. Among authors: miliukhina iv.
Neurobiol Aging. 2018 Nov;71:267.e7-267.e10. doi: 10.1016/j.neurobiolaging.2018.06.027. Epub 2018 Jul 9.
Neurobiol Aging. 2018.
PMID: 30146349
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A low blood copper concentration is a co-morbidity burden factor in Parkinson's disease development.
Ilyechova EY, Miliukhina IV, Orlov IA, Muruzheva ZM, Puchkova LV, Karpenko MN.
Ilyechova EY, et al. Among authors: miliukhina iv.
Neurosci Res. 2018 Oct;135:54-62. doi: 10.1016/j.neures.2017.11.011. Epub 2018 Jan 8.
Neurosci Res. 2018.
PMID: 29203265
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Case of Early-Onset Parkinson's Disease in a Heterozygous Mutation Carrier of the ATP7B Gene.
Ilyechova EY, Miliukhina IV, Karpenko MN, Orlov IA, Puchkova LV, Samsonov SA.
Ilyechova EY, et al. Among authors: miliukhina iv.
J Pers Med. 2019 Aug 17;9(3):41. doi: 10.3390/jpm9030041.
J Pers Med. 2019.
PMID: 31426520
Free PMC article.
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