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The influence of GSTP1 A313G polymorphism on susceptibility, chemotherapy-related toxicity and prognosis of Hodgkin's lymphoma in Ukrainian patients.
Published in:
Biopolymers & Cell, 2012, v. 28, n. 1, p. 56, doi. 10.7124/bc.00002D
By:
- Kriachok, I. A.;
- Khranovska, N. M.;
- Svergun, N. M.;
- Filonenko, K. S.;
- Novosad, O. I.;
- Titorenko, I. B.;
- Martynchik, A. V.;
- Gubareva, H. O.;
- Kadnikova, T. V.;
- Aleksik, O. M.;
- Kushchevyy, E. V.;
- Pastushenko, I. V.
Publication type:
Article
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families.
Published in:
2020
By:
- Rudenskaya, G. E.;
- Kadnikova, V. A.;
- Ryzhkova, O. P.;
- Bessonova, L. A.;
- Dadali, E. L.;
- Guseva, D. S.;
- Markova, T. V.;
- Khmelkova, D. N.;
- Polyakov, A. V.
Publication type:
journal article
Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50911-9
By:
- Kadnikova, V. A.;
- Rudenskaya, G. E.;
- Stepanova, A. A.;
- Sermyagina, I. G.;
- Ryzhkova, O. P.
Publication type:
Article
A new case of infantile‐onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family.
Published in:
European Journal of Neurology, 2019, v. 26, n. 5, p. e61, doi. 10.1111/ene.13880
By:
- Chukhrova, A. L.;
- Akimova, I. A.;
- Shchagina, O. A.;
- Kadnikova, V. A.;
- Ryzhkova, O. P.;
- Polyakov, A. V.
Publication type:
Article
Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia.
Published in:
Russian Journal of Genetics, 2022, v. 58, n. 9, p. 1145, doi. 10.1134/S1022795422090113
By:
- Khidiyatova, I. M.;
- Saifullina, E. V.;
- Karunas, A. S.;
- Akhmetgaleyeva, A. F.;
- Kutlubaeva, R. F.;
- Smakova, L. A.;
- Lobov, S. L.;
- Polyakov, A. V.;
- Shchagina, O. A.;
- Kadnikova, V. A.;
- Ryzhkova, O. P.;
- Magzhanov, R. V.;
- Khusnutdinova, E. K.
Publication type:
Article
Spectrum of pathogenic variants and high prevalence of pathogenic BBS7 variants in Russian patients with Bardet-Biedl syndrome.
Published in:
Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1419025
By:
- Orlova, M.;
- Gundorova, P.;
- Kadnikova, V.;
- Polyakov, A.
Publication type:
Article

Found: 6

The influence of GSTP1 A313G polymorphism on susceptibility, chemotherapy-related toxicity and prognosis of Hodgkin's lymphoma in Ukrainian patients.

KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families.

Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia.

A new case of infantile‐onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family.

Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia.

Spectrum of pathogenic variants and high prevalence of pathogenic BBS7 variants in Russian patients with Bardet-Biedl syndrome.