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Cryo-electron microscopy of extracellular vesicles from cerebrospinal fluid

PloS one, 2020-01, Vol.15 (1), p.e0227949

2020

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A low blood copper concentration is a co-morbidity burden factor in Parkinson’s disease development

Neuroscience research, 2018-10, Vol.135, p.54-62

2018

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Mutation analysis of Parkinson's disease genes in a Russian data set

Neurobiology of aging, 2018-11, Vol.71, p.267.e7-267.e10

2018

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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

International journal of molecular sciences, 2023-05, Vol.24 (10), p.9105

2023

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Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?

Movement disorders, 2022-08, Vol.37 (8), p.1779-1781

2022

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Comparative Transcriptome Analysis in Monocyte-Derived Macrophages of Asymptomatic GBA Mutation Carriers and Patients with GBA-Associated Parkinson's Disease

Genes, 2021-09, Vol.12 (10), p.1545

2021

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The Effect of p.G2019S Mutation in the LRRK2 Gene on the Activity of Lysosomal Hydrolases and the Clinical Features of Parkinson's Disease Associated with p.N370S Mutation in the GBA1 Gene

Journal of integrative neuroscience, 2024-01, Vol.23 (1), p.16-16

2024

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Case of Early-Onset Parkinson's Disease in a Heterozygous Mutation Carrier of the ATP7B Gene

Journal of personalized medicine, 2019-08, Vol.9 (3), p.41

2019

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Postural instability and neuropsychiatric disturbance in the overlapping phenotype of essential tremor and Parkinson's Disease

Neurophysiologie clinique, 2020-11, Vol.50 (6), p.489-494

2020

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Autosomal Dominant Parkinson's Disease Caused by SNCA p. E46K Mutation in a Family with Russian Ancestry

Movement disorders, 2024-08, Vol.39 (8), p.1424-1425

2024

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Increased α‐Synuclein Level in CD45+ Blood Cells in Asymptomatic Carriers of GBA Mutations

Movement disorders, 2021-08, Vol.36 (8), p.1997-1998

2021

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Decreased LAMP2 mRNA levels in CD45+ blood cells in patients with GBA-associated Parkinson’s disease (1815)

Neurology, 2020-04, Vol.94 (15_supplement)

2020

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Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations

Movement disorders, 2018-08, Vol.33 (8), p.1325-1330

2018

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Autosomal Dominant Parkinson's Disease Caused by SNCA p.E46K Mutation in a Family with Russian Ancestry

Movement disorders, 2024-08, Vol.39 (8), p.1424-1425

2024

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Alteration of lysosomal enzymatic activities as risk factor of Parkinson's disease associated with mutations in the GBA gene

Journal of the neurological sciences, 2021-10, Vol.429, p.119577, Article 119577

2021

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Alteration of expression levels of genes involved in maintaining dopaminergic system as trigger for GBA-associated Parkinson's disease

Journal of the neurological sciences, 2021-10, Vol.429, p.119573, Article 119573

2021

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Glucocerebrosidase activity and transport to lysosomes in primary macrophages from patients with mutations in the GBA gene

Journal of the neurological sciences, 2021-10, Vol.429, p.119511, Article 119511

2021

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The use of vortioxetine for depression in patients with Parkinson's disease in the early and advanced stages of the disease

Nevrologii͡a︡, neĭropsikhiatrii͡a︡, psikhosomatika, 2020, Vol.12 (5), p.40-45

Miliukhina, I. V.

2020

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Diagnostic capabilities of posturological methods in extrapyramidal disorders

Medical academic journal, 2020-06, Vol.20 (1), p.45-50

2020

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Profiling the biochemical lysosomal activities in blood of patients with multiple system atrophy

Journal of the neurological sciences, 2021-10, Vol.429, p.117668, Article 117668

2021

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Associations of genetic variants in COMT, BDNF, SNCA, MAPT genes with cognitive impairment in Parkinson’s disease. (P6.090)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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Rare TMEM230 Variants are Potentially Associated With Early Onset Parkinson’s Disease (P3-11.013)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Association of Rare Variants in ARSA with Parkinson's Disease

Movement disorders, 2023-10, Vol.38 (10), p.1806-1812

2023

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The relationship between serum and cerebrospinal fluid inflammatory biomarkers in Parkinson's disease

Parkinsonism & related disorders, 2016-01, Vol.22, p.e31-e32

2016

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Cryo-electron microscopy of extracellular vesicles from cerebrospinal fluid

A low blood copper concentration is a co-morbidity burden factor in Parkinson’s disease development

Mutation analysis of Parkinson's disease genes in a Russian data set

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

Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?

Comparative Transcriptome Analysis in Monocyte-Derived Macrophages of Asymptomatic GBA Mutation Carriers and Patients with GBA-Associated Parkinson's Disease

The Effect of p.G2019S Mutation in the LRRK2 Gene on the Activity of Lysosomal Hydrolases and the Clinical Features of Parkinson's Disease Associated with p.N370S Mutation in the GBA1 Gene

Case of Early-Onset Parkinson's Disease in a Heterozygous Mutation Carrier of the ATP7B Gene

Altered Sphingolipid Hydrolase Activities and Alpha-Synuclein Level in Late-Onset Schizophrenia

Postural instability and neuropsychiatric disturbance in the overlapping phenotype of essential tremor and Parkinson's Disease

Autosomal Dominant Parkinson's Disease Caused by SNCA p. E46K Mutation in a Family with Russian Ancestry

Increased α‐Synuclein Level in CD45+ Blood Cells in Asymptomatic Carriers of GBA Mutations

Decreased LAMP2 mRNA levels in CD45+ blood cells in patients with GBA-associated Parkinson’s disease (1815)

Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations

Autosomal Dominant Parkinson's Disease Caused by SNCA p.E46K Mutation in a Family with Russian Ancestry

Alteration of lysosomal enzymatic activities as risk factor of Parkinson's disease associated with mutations in the GBA gene

Alteration of expression levels of genes involved in maintaining dopaminergic system as trigger for GBA-associated Parkinson's disease

Glucocerebrosidase activity and transport to lysosomes in primary macrophages from patients with mutations in the GBA gene

The use of vortioxetine for depression in patients with Parkinson's disease in the early and advanced stages of the disease

Diagnostic capabilities of posturological methods in extrapyramidal disorders

Profiling the biochemical lysosomal activities in blood of patients with multiple system atrophy

Associations of genetic variants in COMT, BDNF, SNCA, MAPT genes with cognitive impairment in Parkinson’s disease. (P6.090)

Rare TMEM230 Variants are Potentially Associated With Early Onset Parkinson’s Disease (P3-11.013)

Association of Rare Variants in ARSA with Parkinson's Disease

The relationship between serum and cerebrospinal fluid inflammatory biomarkers in Parkinson's disease

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