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DNA methylation in Parkinson disease
Yakovenko E.V., Fedotova E.Y., Illarioshkin S.N.
Gene Expression of Lysosomal Membrane Proteins in Parkinson Disease, Associated with Mutations in the Glucocerebrosidase Gene (GBA)
Usenko T.S., Bezrukova A.I., Bogdanova D.A., Nikolaev M.A., Miliukhina I.V., Gracheva E.V., Senkevich K.A., Zakharova E.Y., Emelyanov A.K., Pchelina S.N.
The use of a pharmabiotic based on the Lactobacillus fermentum U-21 strain to modulate the neurodegenerative process in an experimental model of Parkinson disease
Danilenko V.N., Stavrovskaya A.V., Voronkov D.N., Gushchina A.S., Marsova M.V., Yamshchikova N.G., Ol'shansky А.S., Ivanov M.V., Illarioshkin S.N.
The impact of DRD3, HS1-BP3, and LINGO1 gene mutations on the development and clinical heterogeneity of essential tremor in the Sakha Republic (Yakutia)
Govorova T.G., Popova T.E., Tappakhov A.A., Golikova P.I., Danilova A.L., Antipina U.D., Samorseva V.N., Petrova A.Y., Andreev M.E., Lyasheeva N.N.
Comorbidities in cerebrovascular diseases
Tanashyan M.M., Lagoda O.V., Klushnikov S.A., Zakharova M.N., Maksyutkina L.N.
Cortical cerebral atrophy in patients with Parkinson’s disease: new trends in the diagnostics in vivo
Trufanov A.G., Litvinenko I.V., Odinak M.M., Voronkov L.V., Khaimov D.A., Efimzev A.Y., Fokin V.A.
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