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S A Klyushnikov

Showing results (1-10 of 8) with videos related to

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Biochemistry. Biokhimiia|November 27, 2018
Molecular Pathogenesis in Huntington's DiseaseS N Illarioshkin, S A Klyushnikov, V A Vigont, et al.
European Journal of Neurology|October 29, 2000
Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical featuresS N Illarioshkin, G K Bagieva, S A Klyushnikov, 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.
Cerebellum & Ataxias|January 16, 2016
ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxiaM I Shadrina, M V Shulskaya, S A Klyushnikov, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 19, 2019
[Diagnostic algorithm for autosomal recessive ataxia]E P Nuzhnyi, N Yu Abramycheva, S A Klyushnikov, et al.
Journal of Neurology|July 1, 1996
Spinocerebellar ataxia type 1 in RussiaS N Illarioshkin, P A Slominsky, I V Ovchinnikov, et al.
Stem Cell Research|June 25, 2021
Generation of induced pluripotent stem cell line RCPCMi008-A derived from patient with spinocerebellar ataxia 17L D Shuvalova, A V Davidenko, A V Eremeev, et al.
Mitochondrion|January 24, 2021
Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypesI O Bychkov, Y S Itkis, P G Tsygankova, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Biochemistry. Biokhimiia|November 27, 2018
Molecular Pathogenesis in Huntington's DiseaseS N Illarioshkin, S A Klyushnikov, V A Vigont, et al.
European Journal of Neurology|October 29, 2000
Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical featuresS N Illarioshkin, G K Bagieva, S A Klyushnikov, 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.
Cerebellum & Ataxias|January 16, 2016
ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxiaM I Shadrina, M V Shulskaya, S A Klyushnikov, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 19, 2019
[Diagnostic algorithm for autosomal recessive ataxia]E P Nuzhnyi, N Yu Abramycheva, S A Klyushnikov, et al.
Journal of Neurology|July 1, 1996
Spinocerebellar ataxia type 1 in RussiaS N Illarioshkin, P A Slominsky, I V Ovchinnikov, et al.
Stem Cell Research|June 25, 2021
Generation of induced pluripotent stem cell line RCPCMi008-A derived from patient with spinocerebellar ataxia 17L D Shuvalova, A V Davidenko, A V Eremeev, et al.
Mitochondrion|January 24, 2021
Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypesI O Bychkov, Y S Itkis, P G Tsygankova, et al.
Pageof 1