Correction to: Genetic etiology of non-syndromic hearing loss in Latin America von Lezirovitz, Karina, Mingroni-Netto, Regina Célia

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Genetic etiology of non-syndromic hearing loss in Latin America von Lezirovitz, Karina, Mingroni-Netto, Regina Célia

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Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss von Batissoco, Ana Carla, Pedroso-Campos, Vinicius, Pardono, Eliete, Sampaio-Silva, Juliana, Sonoda, Cindy Yukimi, Vieira-Silva, Gleiciele Alice, da Silva de Oliveira Longati, Estefany Uchoa, Mariano, Diego, Hoshino, Ana Cristina Hiromi, Tsuji, Robinson Koji, Jesus-Santos, Rafaela, Abath-Neto, Osório, Bento, Ricardo Ferreira, Oiticica, Jeanne, Lezirovitz, Karina

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Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss von Bueno, André S, Nunes, Kelly, Dias, Alex M M, Alves, Leandro U, Mendes, Beatriz C A, Sampaio-Silva, Juliana, Smits, Jeroen, Yntema, Helger G, Meyer, Diogo, Lezirovitz, Karina, Mingroni-Netto, Regina C

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Genetic heterogeneity in autosomal recessive hearing loss: a survey of Brazilian families von Antunes, Larissa Nascimento, Dias, Alex Marcel Moreira, Schiavo, Beatriz Cetalle, Mendes, Beatriz C A, Bertola, Debora Romeo, Lezirovitz, Karina, Mingroni-Netto, Regina Célia

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New Insights on the Effect of TNF Alpha Blockade by Gene Silencing in Noise-Induced Hearing Loss von Rodrigues, Janaína C, Bachi, André L L, Silva, Gleiciele A V, Rossi, Marcelo, do Amaral, Jonatas B, Lezirovitz, Karina, de Brito, Rubens

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Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2 von Massucci-Bissoli, Milene, Lezirovitz, Karina, Oiticica, Jeanne, Bento, Ricardo Ferreira

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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-hea... von Kobayashi, Gerson S., Vieira-Silva, Gleiciele A., Varella-Branco, Elisa, Moreira, Danielle P., Kitajima, João Paulo F.W., Hemza, Claudia R.M.L., Mingroni-Netto, Regina C., Lojudice, Fernando H., Oiticica, Jeanne, Bento, Ricardo F., Batissoco, Ana C., Lezirovitz, Karina

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Hearing aid effectiveness on patients with chronic tinnitus and associated hearing loss von Simonetti, Patricia, Vasconcelos, Laura Garcia, Gândara, Mara Rocha, Lezirovitz, Karina, Medeiros, Ítalo Roberto Torres de, Oiticica, Jeanne

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Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans von Dias, Alex Marcel Moreira, Lezirovitz, Karina, Nicastro, Fernanda Stávale, Mendes, Beatriz C A, Mingroni-Netto, Regina Célia

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Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants von Bertani-Torres, William, Lezirovitz, Karina, Alencar-Coutinho, Danillo, Pardono, Eliete, da Costa, Silvia Souza, Antunes, Larissa do Nascimento, de Oliveira, Judite, Otto, Paulo Alberto, Pingault, Véronique, Mingroni-Netto, Regina Célia

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Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing von Soares de Lima, Yasmin, Chiabai, Marcela, Shen, Jun, Córdoba, Mara S., Versiani, Beatriz R., Benício, Rosenelle O.A., Pogue, Robert, Mingroni-Netto, Regina Célia, Lezirovitz, Karina, Pic-Taylor, Aline, Mazzeu, Juliana F., Oliveira, Silviene F.

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Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects von Nonose, Renata Watanabe, Lezirovitz, Karina, de Mello Auricchio, Maria Teresa Balester, Batissoco, Ana Carla, Yamamoto, Guilherme Lopes, Mingroni-Netto, Regina Célia

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Novel OTOF mutations in Brazilian patients with auditory neuropathy von Romanos, Jihane, Kimura, Lilian, Fávero, Mariana Lopes, Izarra, Fernanda Attanasio R, de Mello Auricchio, Maria Teresa Balester, Batissoco, Ana Carla, Lezirovitz, Karina, Abreu-Silva, Ronaldo Serafim, Mingroni-Netto, Regina Célia

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Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea von Oiticica, Jeanne, Barboza-Junior, Luiz Carlos M, Batissoco, Ana Carla, Lezirovitz, Karina, Mingroni-Netto, Regina C, Haddad, Luciana A, Bento, Ricardo F

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c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family von Dantas, Vitor G L, Lezirovitz, Karina, Yamamoto, Guilherme L, Moura de Souza, Carolina Fischinger, Ferreira, Simone Gomes, Mingroni-Netto, Regina C

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Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13 von Macedo-Souza, Lucia I., Kok, Fernando, Santos, Silvana, Amorim, Simone C., Starling, Alessandra, Nishimura, Agnes, Lezirovitz, Karina, Lino, Angelina M. M., Zatz, Mayana

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MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization von de Oliveira Pelegrino, Karla, Sugayama, Sofia, Lezirovitz, Karina, Catelani, Ana Lúcia, Kok, Fernando, de Lourdes Chauffaille, Maria

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7q36 deletion and 9p22 duplication: effects of a double imbalance von Pelegrino, Karla de Oliveira, Sugayama, Sofia, Catelani, Ana Lúcia, Lezirovitz, Karina, Kok, Fernando, Chauffaille, Maria de Lourdes

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Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"? von Lezirovitz, Karina, Nicastro, Fernanda Stávale, Pardono, Eliete, Abreu-Silva, Ronaldo Serafim, Batissoco, Ana Carla, Neustein, Isaac, Spinelli, Mauro, Mingroni-Netto, Regina Célia

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