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2020 1
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Page 1
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia.
Kistol D, Tsygankova P, Krylova T, Bychkov I, Itkis Y, Nikolaeva E, Mikhailova S, Sumina M, Pechatnikova N, Kurbatov S, Bostanova F, Migiaev O, Zakharova E. Kistol D, et al. Among authors: bostanova f. Int J Mol Sci. 2023 Jan 13;24(2):1597. doi: 10.3390/ijms24021597. Int J Mol Sci. 2023. PMID: 36675121 Free PMC article.
The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation.
Kovalskaia VA, Kungurtseva AL, Bostanova FM, Vasiliev PA, Tabakov VY, Orlova MD, Povolotskaya IS, Novoselova OG, Bikanov RA, Akhyamova MA, Tikhonovich YV, Popovich AV, Vitebskaya AV, Dadali EL, Ryzhkova OP. Kovalskaia VA, et al. Among authors: bostanova fm. Genes (Basel). 2024 Jan 29;15(2):180. doi: 10.3390/genes15020180. Genes (Basel). 2024. PMID: 38397171 Free PMC article.
Patients with Papillary Renal Cancer and Germline Duplication of MET Exons 5-21.
Mikhaylenko DS, Kuryakova NB, Bostanova FM, Zabnenkova VV, Ryzhkova OP, Volodin IV, Zaletaev DV, Pustoshilov DV, Kutsev SI, Strelnikov VV. Mikhaylenko DS, et al. Among authors: bostanova fm. Biomedicines. 2025 May 29;13(6):1329. doi: 10.3390/biomedicines13061329. Biomedicines. 2025. PMID: 40564049 Free PMC article.
Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia.
Kovalskaia VA, Cherevatova TB, Zinina EV, Shagina OA, Vorontsova EO, Matyushchenko GN, Demina NA, Petukhova MP, Markova TV, Guseva DM, Galkina VA, Anisimova IV, Stepanova AA, Chuhrova AL, Sharova MV, Bostanova FM, Voskanyan AE, Polyakov AV, Ryzhkova OP. Kovalskaia VA, et al. Among authors: bostanova fm. Orphanet J Rare Dis. 2026 Feb 5;21(1):45. doi: 10.1186/s13023-026-04211-x. Orphanet J Rare Dis. 2026. PMID: 41645317 Free PMC article.
11 results