G E Rudenskaya

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Venues

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

Scientific reports

BMC neurology

Research Centre for Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Research Centre for Medical Genetics Nov 08 1990

Russia

Chief Researcher :: Genetic Counseling Department

Publications

G E Rudenskaya, Daria Guseva, Olga Mironovich, V A Kadnikova, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Oxana P Ryzhkova
[Developmental and epileptic encephalopathy produced by the ATP1A2 mutation]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 124 (6) (2024)
G E Rudenskaya, Daria Guseva, Olga Mironovich, V A Kadnikova, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Oxana P Ryzhkova
[Developmental and epileptic encephalopathy produced by the ATP1A2 mutation]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 124 (6) (2024)
G E Rudenskaya, A S Kuchina, V A Kadnikova, Oxana P Ryzhkova
[A case of spastic paraplegia with SPG4 and SPG3 associated mutations]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 123 (5) (2023)
G E Rudenskaya, M S Petukhova, Viktoriia V Zabnenkova, Tatiana B Cherevatova, Oxana P Ryzhkova
[Early-onset familial Alzheimer's disease with spastic paraparesis associated with PSEN1 gene]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 123 (11) (2023)
G E Rudenskaya, Fedor A Konovalov, Sergey Nikolaevich Illarioshkin, Olga A Shchagina
[Gerstmann-Sträussler disease: a familial case with common PRNP mutation and atypical features]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 123 (2) (2023)
G E Rudenskaya, I G Sermyagina, Alena Chukhrova, E L Dadali, Ekaterina R Tolmacheva, Olga A Shchagina
[Diversity of CACNA1A-related disorders]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 121 (12) (2022)
G E Rudenskaya, E A Shestopalova, V A Kadnikova, Olga A Shchagina
[Atypical spastic paraplegia type 4 due to p.Arg499His mutation in SPAST gene]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 122 (3) (2022)
G E Rudenskaya, Daria Guseva, Olga Mironovich, V A Kadnikova, E L Dadali, I F Komar'kov, Olga G Novoselova, Oxana P Ryzhkova
[AP4-assocated hereditary spastic paraplegias]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 121 (2) (2021)
G E Rudenskaya, V A Kadnikova, L A Bessonova, Peter A Sparber, Sergey Kurbatov, Olga Mironovich, Fedor A Konovalov, Oxana P Ryzhkova
[Autosomal dominant spastic paraplegias]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 121 (5) (2021)
G E Rudenskaya, V A Kadnikova, Oxana P Ryzhkova, L A Bessonova, E L Dadali, Daria Guseva, Tatiana Vladimirovna Markova, D N Khmelkova, Olga A Shchagina
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families. BMC neurology 20 (1) (2020)
V A Kadnikova, G E Rudenskaya, Anna A Stepanova, I G Sermyagina, Oxana P Ryzhkova
Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia. Scientific reports 9 (1) (2019)

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Publication Activity (10 Years)

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G E Rudenskaya