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Auditory Phenotype of a Novel Missense Variant in the CEACAM16 Gene in a Large Russian Family With Autosomal Dominant Nonsyndromic Hearing Loss.
Markova TG, Alekseeva NN, Ryzhkova OP, Shatokhina OL, Orlova AA, Zabnenkova VV, Groznova OS, Sagaydak OV, Chibisova SS, Polyakov AV, Tavartkiladze GA. Markova TG, et al. Among authors: shatokhina ol. J Int Adv Otol. 2024 Mar 27;20(2):119-126. doi: 10.5152/iao.2024.231252. J Int Adv Otol. 2024. PMID: 39157884 Free PMC article.
Early audiological phenotype in patients with mutations in the USH2A gene.
Markova TG, Lalayants MR, Alekseeva NN, Ryzhkova OP, Shatokhina OL, Galeeva NM, Bliznetz EA, Weener ME, Belov OA, Chibisova SS, Polyakov AV, Tavartkiladze GA. Markova TG, et al. Among authors: shatokhina ol. Int J Pediatr Otorhinolaryngol. 2022 Jun;157:111140. doi: 10.1016/j.ijporl.2022.111140. Epub 2022 Apr 15. Int J Pediatr Otorhinolaryngol. 2022. PMID: 35452909
Spectrum of Genes for Non-GJB2-Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.
Shatokhina O, Galeeva N, Stepanova A, Markova T, Lalayants M, Alekseeva N, Tavarkiladze G, Markova T, Bessonova L, Petukhova M, Guseva D, Anisimova I, Polyakov A, Ryzhkova O, Bliznetz E. Shatokhina O, et al. Int J Mol Sci. 2022 Dec 12;23(24):15748. doi: 10.3390/ijms232415748. Int J Mol Sci. 2022. PMID: 36555390 Free PMC article.
[Developmental and epileptic encephalopathy produced by the ATP1A2 mutation].
Rudenskaya GE, Guseva DM, Shatokhina OL, Kadnikova VA, Filatova AY, Skoblov MY, Ryzhkova OP. Rudenskaya GE, et al. Among authors: shatokhina ol. Zh Nevrol Psikhiatr Im S S Korsakova. 2024;124(6):133-138. doi: 10.17116/jnevro2024124061133. Zh Nevrol Psikhiatr Im S S Korsakova. 2024. PMID: 39072579 Russian.
12 results