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Gene Expression of Lysosomal Membrane Proteins in Parkinson Disease, Associated with Mutations in the Glucocerebrosidase Gene (GBA)
Usenko T., Bezrukova A., Bogdanova D., Nikolaev M., Miliukhina I., Gracheva E., Senkevich K., Zakharova E., Emelyanov A., Pchelina S.
Examining the frequency of dysphagia and the predictive factors of dysphagia that require attention in patients with Parkinson's disease
Babajani Roshan T., Behzad C., Saadat P., Bijani A., Dehghan M., Ahmadi Ahangar A.
Cortical cerebral atrophy in patients with Parkinson’s disease: new trends in the diagnostics in vivo
Trufanov A., Litvinenko I., Odinak M., Voronkov L., Khaimov D., Efimzev A., Fokin V.
Comorbidities in cerebrovascular diseases
Tanashyan M., Lagoda O., Klyushnikov S., Zakharova M., Maksyutkina L.
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., Stavrovskaya A., Voronkov D., Gushchina A., Marsova M., Yamshchikova N., Ol'shansky А., Ivanov M., Illarioshkin S.
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., Popova T., Tappakhov A., Golikova P., Danilova A., Antipina U., Samorseva V., Petrova A., Andreev M., Lyasheeva N.
DNA methylation in Parkinson disease
Yakovenko E., Fedotova E., Illarioshkin S.
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