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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2006 1
2007 1
2008 5
2009 3
2010 1
2011 1
2012 3
2013 1
2014 1
2015 2
2016 1
2017 2
2018 7
2019 1
2020 2
2021 3
2022 6
2023 2
2024 1

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37 results

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Page 1
New Insights into the Identity of the DFNA58 Gene.
Nascimento LRD, Vieira-Silva GA, Kitajima JPFW, Batissoco AC, Lezirovitz K. Nascimento LRD, et al. Among authors: lezirovitz k. Genes (Basel). 2022 Dec 2;13(12):2274. doi: 10.3390/genes13122274. Genes (Basel). 2022. PMID: 36553541 Free PMC article.
Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing.
Chen H, Monga M, Fang Q, Slitin L, Neef J, Chepurwar SS, Netto RCM, Lezirovitz K, Tabith A Jr, Benseler F, Brose N, Kusch K, Wichmann C, Strenzke N, Vona B, Preobraschenski J, Moser T. Chen H, et al. Among authors: lezirovitz k. Protein Cell. 2024 Apr 1;15(4):305-312. doi: 10.1093/procel/pwad058. Protein Cell. 2024. PMID: 38066594 Free PMC article. No abstract available.
Hearing aid effectiveness on patients with chronic tinnitus and associated hearing loss.
Simonetti P, Vasconcelos LG, Gândara MR, Lezirovitz K, Medeiros ÍRT, Oiticica J. Simonetti P, et al. Among authors: lezirovitz k. Braz J Otorhinolaryngol. 2022 Nov-Dec;88 Suppl 3(Suppl 3):S164-S170. doi: 10.1016/j.bjorl.2022.03.002. Epub 2022 May 20. Braz J Otorhinolaryngol. 2022. PMID: 35729042 Free PMC article. Clinical Trial.
Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss.
Batissoco AC, Pedroso-Campos V, Pardono E, Sampaio-Silva J, Sonoda CY, Vieira-Silva GA, da Silva de Oliveira Longati EU, Mariano D, Hoshino ACH, Tsuji RK, Jesus-Santos R, Abath-Neto O, Bento RF, Oiticica J, Lezirovitz K. Batissoco AC, et al. Among authors: lezirovitz k. Hum Genet. 2022 Apr;141(3-4):519-538. doi: 10.1007/s00439-021-02372-2. Epub 2021 Oct 1. Hum Genet. 2022. PMID: 34599368
Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing.
Soares de Lima Y, Chiabai M, Shen J, Córdoba MS, Versiani BR, Benício ROA, Pogue R, Mingroni-Netto RC, Lezirovitz K, Pic-Taylor A, Mazzeu JF, Oliveira SF. Soares de Lima Y, et al. Among authors: lezirovitz k. Hear Res. 2018 Dec;370:181-188. doi: 10.1016/j.heares.2018.10.008. Epub 2018 Oct 16. Hear Res. 2018. PMID: 30390570
Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A).
Kobayashi GS, Vieira-Silva GA, Varella-Branco E, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni-Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. Kobayashi GS, et al. Among authors: lezirovitz k. Stem Cell Res. 2023 Sep;71:103181. doi: 10.1016/j.scr.2023.103181. Epub 2023 Aug 9. Stem Cell Res. 2023. PMID: 37595341 Free article.
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58.
Lezirovitz K, Vieira-Silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Pedroso-Campos V, Nascimento LR, Sonoda CY, Borges VM, Vasconcelos LG, Beck RMO, Grasel SS, Jagger DJ, Grillet N, Bento RF, Mingroni-Netto RC, Oiticica J. Lezirovitz K, et al. Hum Mol Genet. 2020 Jun 3;29(9):1520-1536. doi: 10.1093/hmg/ddaa075. Hum Mol Genet. 2020. PMID: 32337552 Free PMC article.
37 results