Karina Lezirovitz

Tätigkeit: Forscher

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Artikel 29

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2022-05-15

Hearing aid effectiveness on patients with chronic tinnitus and associated hearing loss

Karina Lezirovitz, Jeanne Oiticica
2022-01-15

Correction to: Genetic etiology of non-syndromic hearing loss in Latin America

Karina Lezirovitz
2021-07-02

Cochlea cell-specific marker expression upon in vitro Hes1 knockdown

Ana C Batissoco, Karina Lezirovitz, Daniela B. Zanatta, Luciana Dos Reis Vasques, Bryan E Strauss, Regina Celia Mingroni Netto, Ricardo Ferreira Bento, Jeanne Oiticica
2021-05-06

Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss

Karina Lezirovitz, Regina Celia Mingroni Netto
2021-10-01

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss

Ana C Batissoco, Diego C B Mariano, Osorio Abath Neto, Ricardo Ferreira Bento, Jeanne Oiticica, Karina Lezirovitz
2021-10-15

Genetic etiology of non-syndromic hearing loss in Latin America

Karina Lezirovitz
2020-04-13

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

Janaína C Rodrigues, André Luis Lacerda Bachi, Jônatas do Bussador Amaral, Karina Lezirovitz
2018-06-07

Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss

Angela Ballesteros, Karina Lezirovitz, Regina Celia Mingroni Netto
2018-10-16

Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing

Jun Shen, Robert Pogue, Regina Celia Mingroni Netto, Karina Lezirovitz, Aline Pic-Taylor, Silviene F Oliveira
2018-12-04

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

Karina Lezirovitz, Regina Celia Mingroni Netto
2018-12-01

Polyethylene Glycol fusion associated with anti-oxidants: A new promise in the treatment of traumatic paralysis

Karina Lezirovitz
2017-11-01

Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2

Karina Lezirovitz, Jeanne Oiticica
2017-10-17

Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family

Osorio Abath Neto, Jeanne Oiticica, Karina Lezirovitz
2016-03-18

Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results.

Karina Lezirovitz, Bryan E Strauss, Regina Celia Mingroni Netto, Jeanne Oiticica, Ricardo Ferreira Bento
2015-04-30

Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family.

Karina Lezirovitz, Jeanne Oiticica, Carla Rosenberg, Regina Celia Mingroni Netto
2014-10-01

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family

Karina Lezirovitz, Regina Celia Mingroni Netto
2013-01-15

7q36 deletion and 9p22 duplication: effects of a double imbalance

Karina Lezirovitz
2012-08-01

MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization

Karina Lezirovitz
2011-12-06

Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion

Sigmar Stricker, Eva Klopocki, Charlotte W Ockeloen, Karina Lezirovitz, Regina Celia Mingroni Netto, Aleksander Jamsheer, Hitesh Shah, Ingo Kurth, Outi Mäkitie, Stylianos Antonarakis, Stefan Mundlos, Denise Horn, Anna Rajab
2009-05-22

Novel OTOF mutations in Brazilian patients with auditory neuropathy

Karina Lezirovitz, Regina Celia Mingroni Netto
2009-01-21

A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21

Karina Lezirovitz, Paulo A Otto, Regina Celia Mingroni Netto
2009-02-01

Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling

Karina Lezirovitz, Regina Celia Mingroni Netto
2009-03-04

Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes

Silvana Santos, Karina Lezirovitz, Paulo A Otto, Mayana Zatz
2008-09-01

Study of a Brazilian family presenting non-syndromic hearing loss with mitochondrial inheritance

Karina Lezirovitz
2008-12-01

A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects

Silvana Santos, Karina Lezirovitz, Regina Celia Mingroni Netto, Paulo A Otto, John Marius Opitz
2008-05-08

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

Silvana Santos, Karina Lezirovitz, Mayana Zatz
2008-05-21

A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3.

Karina Lezirovitz, Paulo A Otto, Regina Celia Mingroni Netto
2006-03-20

Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment"

Karina Lezirovitz, Paulo A Otto, Regina Celia Mingroni Netto
2005-05

Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13

Mayana Zatz, Agnes Lumi Nishimura, Silvana Santos, Karina Lezirovitz

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