Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology von Svidnicki, Maria Carolina Costa Melo, Silva-Costa, Sueli Matilde, Ramos, Priscila Zonzini, dos Santos, Nathalia Zocal Pereira, Martins, Fábio Tadeu Arrojo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Hearing preservation and cochlear implants according to inner ear approach: multicentric evaluation von Guimarães, Alexandre Caixeta, de Carvalho, Guilherme Machado, Duarte, Alexandre S.M., Bianchini, Walter A., Sarasty, Andrea Bravo, di Gregorio, Maria Fernanda, Zernotti, Mario Emilio, Sartorato, Edi Lúcia, Castilho, Arthur Menino

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A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene von Martins, Fábio Tadeu Arrojo, Ramos, Berenice Dias, Sartorato, Edi Lúcia

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Ménièreʼs Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients von Lopes, Karen de Carvalho, Sartorato, Edi Lúcia, da Silva-Costa, Sueli M, de Macedo Adamov, Nadya Soares, Ganança, Fernando Freitas

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Genetics of Deafness von Sartorato, Edi Lúcia, Friderici, Karen, Del Castillo, Ignacio

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Molecular study in Brazilian cochlear implant recipients von Christiani, Thalita Vitachi, Alexandrino, Fabiana, de Oliveira, Camila Andréa, Amantini, Regina Célia Bortoleto, Bevilacqua, Maria Cecília, Filho, Orozimbo Alves Costa, Porto, Paulo, Sartorato, a. Edi Lúcia

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Optimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON) von Martins, Fábio Tadeu Arrojo, Miranda, Paulo Maurício do Amor Divino, Fernandes, Marcela Scabello Amaral, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia

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Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform von Martins, Fábio Tadeu Arrojo, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy von Miranda, Paulo Maurício do Amôr Divino, Matilde da Silva-Costa, Sueli, Balieiro, Juliane Cristina, Fernandes, Marcela Scabello Amaral, Alves, Rogério Marins, Guerra, Andrea Trevas Maciel, Marcondes, Ana Maria, Sartorato, Edi Lúcia

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Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry von Alves, Rogério Marins, da Silva Costa, Sueli Matilde, do Amôr Divino Miranda, Paulo Mauricio, Ramos, Priscila Zonzini, Marconi, Thiago Gibbin, Santos Oliveira, Gisele, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Single Nucleotide Polymorphisms of the GJB2 and GJB6 Genes Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss von de Oliveira, Camila Andréa, da Silva-Costa, Sueli Matilde, Medrano, Ruan Felipe Vieira, de Carvalho, Gabriela Queila, de Oliveira, Flávia Marcorin, Grillo, Ana Paula, Sartorato, Edi Lúcia

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Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: Identification of two novel mutations in Brazilian patients von de Moraes, Vanessa Cristine Sousa, dos Santos, Nathalia Zocal Pereira, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Differentiating Leber Hereditary Optic Neuropathy from Normal-Tension Glaucoma von Souto, Fernanda Maria Silveira, de Vasconcellos, José Paulo Cabral, de Melo, Mônica Barbosa, Sartorato, Edi Lúcia, Moura, Frederico Castelo

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Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy von Amaral-Fernandes, Marcela Scabello, Marcondes, Ana Maria, do Amor Divino Miranda, Paulo Maurício, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia

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Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment von de Moraes, Vanessa Cristine Sousa, Alexandrino, Fabiana, Andrade, Paula Baloni, Câmara, Marília Fontenele, Sartorato, Edi Lúcia

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Genetic and audiologic study in elderly with sensorineural hearing loss von Martins, Kelly, Fontenele, Marília, Câmara, Silva, Sartorato, Edi Lúcia

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Searching for digenic inheritance in deaf Brazilian individuals using the multiplex ligation-dependent probe amplification technique von da Silva-Costa, Sueli M, Martins, Fábio Tadeu Arrojo, Pereira, Tânia, Pomilio, Mariza C A, Marques-de-Faria, Antonia Paula, Sartorato, Edi Lúcia

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Connexin mutations in Brazilian patients with skin disorders with or without hearing loss von Alexandrino, Fabiana, de Oliveira, Camila Andréa, Magalhães, Renata F., Florence, Michelle E.B., de Souza, Elemir M., Sartorato, Edi Lúcia

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G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome von Alexandrino, Fabiana, Sartorato, Edi Lúcia, Marques-de-Faria, Antonia Paula, Steiner, Carlos Eduardo

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Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness von Belintani Piatto, Vânia, Maria Goloni Bertollo, Eny, Lúcia Sartorato, Edi, Victor Maniglia, José

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