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Acta Naturae
|
August 4, 2020
The SNCA-Rep1 Polymorphic Locus: Association with the Risk of Parkinson's Disease and SNCA Gene Methylation
E V Iakovenko, N Yu Abramycheva, E Yu Fedotova, et al.
Acta Naturae
|
November 9, 2022
MicroRNA Expression Profile Changes in the Leukocytes of Parkinson's Disease Patients
N S Ardashirova, N Yu Abramycheva, E Yu Fedotova, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
January 18, 2022
[Spinocerebellar ataxia 17: full phenotype in a 42 CAG/CAA-repeats carrier]
D V I, T N Proskokova, N V Sikora, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
September 13, 2024
[Rare forms of autosomal recessive spinocerebellar ataxia associated with mutations in the ANO10 (ATX-ANO10) and SYNE1 (ATX-SYNE1) genes]
E P Nuzhnyi, A O Protopopova, N Yu Abramycheva, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
June 16, 2017
[Differential diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]
A A Moroz, N Yu Abramycheva, M S Stepanova, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
August 29, 2022
[Spinocerebellar ataxia type 8 in Russian patients]
E P Nuzhnyi, N Yu Abramycheva, I A Chkhartishvili, et al.
Bulletin of Experimental Biology and Medicine
|
October 19, 2019
Effect of Mutations in SOD1 and C9orf72 Genes on Autophagy in Lymphomonocytes in Myotrophic Lateral Sclerosis
I A Kochergin, Yu A Shpilyukova, E V Lysogorskaia, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
February 28, 2020
[Epigenetic regulation of clinical manifestations of Friedreich's disease]
E P Nuzhny, N Yu Abramycheva, N S Nikolaeva, et al.
Bulletin of Experimental Biology and Medicine
|
September 29, 2020
C9orf72 Gene Expression in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Yu A Shpilyukova, E Yu Fedotova, N Yu Abramycheva, et al.
Stem Cell Research
|
January 19, 2019
Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease
E V Grigor'eva, T B Malankhanova, A Surumbayeva, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Acta Naturae
|
August 4, 2020
The SNCA-Rep1 Polymorphic Locus: Association with the Risk of Parkinson's Disease and SNCA Gene Methylation
E V Iakovenko, N Yu Abramycheva, E Yu Fedotova, et al.
Acta Naturae
|
November 9, 2022
MicroRNA Expression Profile Changes in the Leukocytes of Parkinson's Disease Patients
N S Ardashirova, N Yu Abramycheva, E Yu Fedotova, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
January 18, 2022
[Spinocerebellar ataxia 17: full phenotype in a 42 CAG/CAA-repeats carrier]
D V I, T N Proskokova, N V Sikora, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
September 13, 2024
[Rare forms of autosomal recessive spinocerebellar ataxia associated with mutations in the ANO10 (ATX-ANO10) and SYNE1 (ATX-SYNE1) genes]
E P Nuzhnyi, A O Protopopova, N Yu Abramycheva, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
June 16, 2017
[Differential diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]
A A Moroz, N Yu Abramycheva, M S Stepanova, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
August 29, 2022
[Spinocerebellar ataxia type 8 in Russian patients]
E P Nuzhnyi, N Yu Abramycheva, I A Chkhartishvili, et al.
Bulletin of Experimental Biology and Medicine
|
October 19, 2019
Effect of Mutations in SOD1 and C9orf72 Genes on Autophagy in Lymphomonocytes in Myotrophic Lateral Sclerosis
I A Kochergin, Yu A Shpilyukova, E V Lysogorskaia, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|
February 28, 2020
[Epigenetic regulation of clinical manifestations of Friedreich's disease]
E P Nuzhny, N Yu Abramycheva, N S Nikolaeva, et al.
Bulletin of Experimental Biology and Medicine
|
September 29, 2020
C9orf72 Gene Expression in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Yu A Shpilyukova, E Yu Fedotova, N Yu Abramycheva, et al.
Stem Cell Research
|
January 19, 2019
Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease
E V Grigor'eva, T B Malankhanova, A Surumbayeva, et al.
Page
of 2