Alekseeva N - Search Results

1

Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.

Markova T, Alekseeva N, Lalayants M, Ryzhkova O, Shatokhina O, Galeeva N, Bliznetz E, Belov O, Chibisova S, Polyakov A, Tavartkiladze G. Markova T, et al. Among authors: alekseeva n. J Pers Med. 2022 Nov 4;12(11):1843. doi: 10.3390/jpm12111843. J Pers Med. 2022. PMID: 36579563 Free PMC article.

2

[Epidemiology of hearing loss in children of the first year of life].

Chibisova SS, Markova TG, Alekseeva NN, Yasinskaya AA, Tsygankova ER, Bliznetz EA, Polyakov AV, Tavartkiladze GA. Chibisova SS, et al. Among authors: alekseeva nn. Vestn Otorinolaringol. 2018;83(4):37-42. doi: 10.17116/otorino201883437. Vestn Otorinolaringol. 2018. PMID: 30113578 Russian.

3

[Hearing loss due to mutations or lack of the gene coding protein stereocillin].

Markova TG, Alekseeva NN, Mironovich OL, Bliznets EA, Lalayants MR, Polyakov AV, Tavartkiladze GA. Markova TG, et al. Among authors: alekseeva nn. Vestn Otorinolaringol. 2020;85(2):14-20. doi: 10.17116/otorino20208502114. Vestn Otorinolaringol. 2020. PMID: 32476383 Russian.

4

Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population.

Markova TG, Alekseeva NN, Mironovich OL, Galeeva NM, Lalayants MR, Bliznetz EA, Chibisova SS, Polyakov AV, Tavartkiladze GA. Markova TG, et al. Among authors: alekseeva nn. Int J Pediatr Otorhinolaryngol. 2020 Nov;138:110247. doi: 10.1016/j.ijporl.2020.110247. Epub 2020 Jul 19. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32705992

5

[Hearing loss due to mutations in the genes responsible for Usher syndrome].

Markova TG, Alekseeva NN, Belov OA, Chugunova TI, Tsygankova ER. Markova TG, et al. Among authors: alekseeva nn. Vestn Otorinolaringol. 2022;87(1):52-59. doi: 10.17116/otorino20228701152. Vestn Otorinolaringol. 2022. PMID: 35274893 Russian.

6

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: alekseeva nn. 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

7

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. Among authors: alekseeva n. Int J Mol Sci. 2022 Dec 12;23(24):15748. doi: 10.3390/ijms232415748. Int J Mol Sci. 2022. PMID: 36555390 Free PMC article.

8

[New method for analysis and visualization of the fine temporal structure of the transient evoked otoacoustic emission signal].

Belov OA, Alekseeva NN, Tavartkiladze GA. Belov OA, et al. Among authors: alekseeva nn. Vestn Otorinolaringol. 2014;(2):58-62. Vestn Otorinolaringol. 2014. PMID: 24781174 Russian.

9

[The experience gained by the Audiology Department with the organization of education, training, and enhancement of the skills for the performance of audiological screening of the newborn infants].

Alekseeva NN, Markova MV, Tsygankova EP, Tavartkiladze GA. Alekseeva NN, et al. Vestn Otorinolaringol. 2014;(3):80. Vestn Otorinolaringol. 2014. PMID: 25246218 Russian. No abstract available.

10

Involvement of Mast Cells in the Pathology of COVID-19: Clinical and Laboratory Parallels.

Budnevsky AV, Avdeev SN, Kosanovic D, Ovsyannikov ES, Savushkina IA, Alekseeva NG, Feigelman SN, Shishkina VV, Filin AA, Esaulenko DI, Perveeva IM. Budnevsky AV, et al. Among authors: alekseeva ng. Cells. 2024 Apr 19;13(8):711. doi: 10.3390/cells13080711. Cells. 2024. PMID: 38667325 Free PMC article.

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