Lezirovitz K[au] - Search Results

Year	Number of Results
2005	1
2006	3
2007	1
2008	5
2009	4
2010	1
2011	2
2012	3
2013	1
2014	1
2015	2
2016	2
2017	2
2018	7
2019	1
2020	2
2021	4
2022	5

1

Cochlea cell-specific marker expression upon in vitro Hes1 knockdown.

Batissoco AC, Lezirovitz K, Zanatta DB, Hemza CRML, Vasques LR, Strauss BE, Mingroni-Netto RC, Haddad LA, Bento RF, Oiticica J. Batissoco AC, et al. Among authors: lezirovitz k. Braz J Med Biol Res. 2021 May 17;54(7):e10579. doi: 10.1590/1414-431X2020e10579. eCollection 2021. Braz J Med Biol Res. 2021. PMID: 34008754 Free PMC article.

2

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.

3

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

4

Genetic etiology of non-syndromic hearing loss in Latin America.

Lezirovitz K, Mingroni-Netto RC. Lezirovitz K, et al. Hum Genet. 2022 Apr;141(3-4):539-581. doi: 10.1007/s00439-021-02354-4. Epub 2021 Oct 15. Hum Genet. 2022. PMID: 34652575 Review.

5

New Insights on the Effect of TNF Alpha Blockade by Gene Silencing in Noise-Induced Hearing Loss.

Rodrigues JC, Bachi ALL, Silva GAV, Rossi M, do Amaral JB, Lezirovitz K, de Brito R. Rodrigues JC, et al. Among authors: lezirovitz k. Int J Mol Sci. 2020 Apr 13;21(8):2692. doi: 10.3390/ijms21082692. Int J Mol Sci. 2020. PMID: 32294929 Free PMC article.

6

Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects.

Nonose RW, Lezirovitz K, de Mello Auricchio MTB, Batissoco AC, Yamamoto GL, Mingroni-Netto RC. Nonose RW, et al. Among authors: lezirovitz k. BMC Med Genet. 2018 May 8;19(1):73. doi: 10.1186/s12881-018-0585-x. BMC Med Genet. 2018. PMID: 29739340 Free PMC article.

7

Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans.

Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni-Netto RC. Dias AMM, et al. Among authors: lezirovitz k. J Hum Genet. 2019 Mar;64(3):257-260. doi: 10.1038/s10038-018-0546-4. Epub 2018 Dec 4. J Hum Genet. 2019. PMID: 30514912

8

fosI Is a New Integron-Associated Gene Cassette Encoding Reduced Susceptibility to Fosfomycin.

Pelegrino Kde O, Campos JC, Sampaio SC, Lezirovitz K, Seco BM, Pereira Mde O, Rocha DA, Jové T, Nicodemo AC, Sampaio JL. Pelegrino Kde O, et al. Among authors: lezirovitz k. Antimicrob Agents Chemother. 2015 Nov 9;60(1):686-8. doi: 10.1128/AAC.02437-15. Print 2016 Jan. Antimicrob Agents Chemother. 2015. PMID: 26552984 Free PMC article.

9

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 May 20:S1808-8694(22)00040-4. doi: 10.1016/j.bjorl.2022.03.002. Online ahead of print. Braz J Otorhinolaryngol. 2022. PMID: 35729042 Free article.

10

Polyethylene glycol fusion associated with antioxidants: A new promise in the treatment of traumatic facial paralysis.

Salomone R, Jácomo AL, Nascimento SBD, Lezirovitz K, Hojaij FC, Costa HJZR, Bento RF. Salomone R, et al. Among authors: lezirovitz k. Head Neck. 2018 Jul;40(7):1489-1497. doi: 10.1002/hed.25122. Epub 2018 Mar 9. Head Neck. 2018. PMID: 29522265

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