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Lezirovitz, Karina
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1

Waardenburg Syndrome: The Contribution of Next-Generation S..:

Bertani-Torres, William ; Lezirovitz, Karina ; Alencar-Coutinho, Danillo...
Audiology Research.  14 (2023)  1 - p. 9-25 , 2023
Link: https://doi.org/10.3390/..
 
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2

Ca2+ binding to the C2E domain of otoferlin is required for..:

Chen, Han ; Monga, Mehar ; Fang, Qinghua...
Protein & Cell.  15 (2023)  4 - p. 305-312 , 2023
Link: https://doi.org/10.1093/..
 
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3

Generation of four induced pluripotent stem cells lines fro..:

Kobayashi, Gerson S. ; Vieira-Silva, Gleiciele A. ; Varella-Branco, Elisa...
Stem Cell Research.  71 (2023)  - p. 103181 , 2023
Link: https://doi.org/10.1016/..
 
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4

New Insights into the Identity of the DFNA58 Gene:

Nascimento, Larissa Reis do ; Vieira-Silva, Gleiciele Alice ; Kitajima, João Paulo Fumio Whitaker..
Genes.  13 (2022)  12 - p. 2274 , 2022
Link: https://doi.org/10.3390/..
 
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5

Hearing aid effectiveness on patients with chronic tinnitus..:

Simonetti, Patricia ; Vasconcelos, Laura Garcia ; Gândara, Mara Rocha...
Brazilian Journal of Otorhinolaryngology.  88 (2022)  - p. S164-S170 , 2022
Link: https://doi.org/10.1016/..
 
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6

Correction to: Genetic etiology of non-syndromic hearing lo..:

Lezirovitz, Karina ; Mingroni-Netto, Regina Célia
Human Genetics.  , 2022
Link: https://doi.org/10.1007/..
 
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7

Genetic etiology of non-syndromic hearing loss in Latin Ame..:

Lezirovitz, Karina ; Mingroni-Netto, Regina Célia
Human Genetics.  , 2021
Link: https://doi.org/10.1007/..
 
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8

Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A v..:

Bueno, André S. ; Nunes, Kelly ; Dias, Alex M. M....
European Journal of Human Genetics.  30 (2021)  1 - p. 13-21 , 2021
Link: https://doi.org/10.1038/..
 
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9

Molecular and genetic characterization of a large Brazilian..:

Batissoco, Ana Carla ; Pedroso-Campos, Vinicius ; Pardono, Eliete...
Human Genetics.  , 2021
Link: https://doi.org/10.1007/..
 
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10

New Insights on the Effect of TNF Alpha Blockade by Gene Si..:

Rodrigues, Janaína C. ; Bachi, André L. L. ; Silva, Gleiciele A. V....
International Journal of Molecular Sciences.  21 (2020)  8 - p. 2692 , 2020
Link: https://doi.org/10.3390/..
 
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11

A rare genomic duplication in 2p14 underlies autosomal domi..:

Oiticica, Jeanne ; Mingroni-Netto, Regina C ; Bento, Ricardo F...
Human Molecular Genetics.  29 (2020)  9 - p. 1520-1536 , 2020
Link: https://doi.org/10.1093/..
 
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12

Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian ..:

Nonose, Renata Watanabe ; Lezirovitz, Karina ; de Mello Auricchio, Maria Teresa Balester...
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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13

Polyethylene glycol fusion associated with antioxidants: A ..:

Salomone, Raquel ; Jácomo, Alfredo Luiz ; Nascimento, Silvia Bona do...
Head & Neck.  40 (2018)  7 - p. 1489-1497 , 2018
Link: https://doi.org/10.1002/..
 
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14

Syndromic hearing loss molecular diagnosis: Application of ..:

Soares de Lima, Yasmin ; Chiabai, Marcela ; Shen, Jun...
Hearing Research.  370 (2018)  - p. 181-188 , 2018
Link: https://doi.org/10.1016/..
 
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15

Characterization of a novel MYO3A missense mutation associa..:

Dantas, Vitor G. L. ; Raval, Manmeet H. ; Ballesteros, Angela...
Scientific Reports.  8 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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