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Vol 14, No 3 (2022)
MicroRNA Expression Profile Changes in the Leukocytes of Parkinson’s Disease Patients
Ardashirova N.S., Abramycheva N.Y., Fedotova E.Y., Illarioshkin S.N.
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Vol 13, No 3 (2021)
A Mouse Model of Nigrostriatal Dopaminergic Axonal Degeneration As a Tool for Testing Neuroprotectors
Kolacheva A.A., Ugrumov M.V.
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Vol 13, No 3 (2021)
A Monoiodotyrosine Challenge Test in a Parkinson’s Disease Model
Kim A.R., Pavlova E.N., Blokhin V.E., Bogdanov V.V., Ugrumov M.V.
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Vol 12, No 2 (2020)
The SNCA-Rep1 Polymorphic Locus: Association with the Risk of Parkinson’s Disease and SNCA Gene Methylation
Iakovenko E.V., Abramycheva N.Y., Fedotova E.Y., Illarioshkin S.N.
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Vol 13, No 2 (2021)
Parkinson’s Disease Associated with GBA Gene Mutations: Molecular Aspects and Potential Treatment Approaches
Senkevich K.A., Kopytova A.E., Usenko T.S., Emelyanov A.K., Pchelina S.N.
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Vol 10, No 3 (2018)
Biochemical and Functional Changes in the Eye As a Manifestation of Systemic Degeneration of the Nervous System in Parkinsonism
Kim A.R., Pavlenko T.A., Katargina L.A., Chesnokova N.B., Ugrumov M.V.
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Vol 12, No 2 (2020)
Molecular Mechanisms and Clinical Manifestations of Catecholamine Dysfunction in the Eye in Parkinson’s Disease As a Basis for Developing Early Diagnosis
Pavlenko T.А., Chesnokova N.B., Nodel M.R., Kim A.R., Ugrumov M.V.
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(Eng)
Vol 11, No 4 (2019)
Tear Fluid Catecholamines As Biomarkers of the Parkinson’s Disease: A Clinical and Experimental Study
Kim A.R., Nodel M.R., Pavlenko T.A., Chesnokova N.B., Yakhno N.N., Ugrumov M.V.
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(Rus)
Vol 7, No 4 (2015)
Mutations in the Parkinson’s Disease-Associated PARK2 Gene Are Accompanied by Imbalance in Programmed Cell Death Systems
Konovalova E.V., Lopacheva O.M., Grivennikov I.A., Lebedeva O.S., Dashinimaev E.В., Khaspekov L.G., Fedotova E.Y., Illarioshkin S.N.
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