Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology
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
Published in BMC medical genetics (23.09.2015)
Published in BMC medical genetics (23.09.2015)
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Hearing preservation and cochlear implants according to inner ear approach: multicentric evaluation
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
Published in Brazilian journal of otorhinolaryngology (01.03.2015)
Published in Brazilian journal of otorhinolaryngology (01.03.2015)
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Genetics of Deafness
Sartorato, Edi Lúcia, Friderici, Karen, Del Castillo, Ignacio
Published in Genetics Research International (01.01.2012)
Published in Genetics Research International (01.01.2012)
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Molecular study in Brazilian cochlear implant recipients
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
Published in American journal of medical genetics. Part A (15.07.2007)
Published in American journal of medical genetics. Part A (15.07.2007)
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Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients
Lopes, Karen de Carvalho, Sartorato, Edi Lúcia, da Silva-Costa, Sueli M, de Macedo Adamov, Nadya Soares, Ganança, Fernando Freitas
Published in Otology & neurotology (01.09.2016)
Published in Otology & neurotology (01.09.2016)
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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)
Martins, Fábio Tadeu Arrojo, Miranda, Paulo Maurício do Amor Divino, Fernandes, Marcela Scabello Amaral, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia
Published in Molecular vision (21.07.2017)
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Published in Molecular vision (21.07.2017)
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Interaction between audiology and genetics in the study of a family: the complexity of molecular diagnosis and genetic counseling
Hoffmann, Flavia Maria Rodrigues, Rodrigues, Patrícia Fernandes, dos Santos, Teresa Maria Momensohn, Sartorato, Edi Lucia, Maciel-Guerra, Andréa Trevas, Matas, Carla Gentile, de Moraes, Vanessa Cristine Sousa
Published in Brazilian journal of otorhinolaryngology (01.09.2008)
Published in Brazilian journal of otorhinolaryngology (01.09.2008)
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Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy
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
Published in Molecular vision (13.08.2016)
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Published in Molecular vision (13.08.2016)
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Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry
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
Published in BMC medical genetics (26.05.2016)
Published in BMC medical genetics (26.05.2016)
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Single Nucleotide Polymorphisms of the GJB2 and GJB6 Genes Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss
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
Published in BioMed research international (01.01.2015)
Published in BioMed research international (01.01.2015)
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Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform
Martins, Fábio Tadeu Arrojo, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lúcia
Published in BMC medical genetics (24.10.2013)
Published in BMC medical genetics (24.10.2013)
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Etiologic and diagnostic evaluation: algorithm for severe to profound sensorineural hearing loss in Brazil
Ramos, Priscila Zonzini, de Moraes, Vanessa Cristine Sousa, Svidnicki, Maria Carolina Costa Melo, Soki, Marcelo Naoki, Castilho, Arthur Menino, Sartorato, Edi Lúcia
Published in International journal of audiology (01.11.2013)
Published in International journal of audiology (01.11.2013)
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Programa de saúde auditiva em neonatos que permaneceram em UTI e/ou cuidados intermediários
Colella-Santos, Maria Francisca, Sartorato, Edi Lucia, Tazinazzio, Tatiana Guilhermino, Françozo, Maria de Fátima de Campos, Couto, Christiane Marques do, Castilho, Arthur Menino, Rosa, Izilda Rodrigues Machado, Lima, Maria Cecilia Marconi Pinheiro, Marba, Sérgio Tadeu Martins
Published in Brazilian journal of otorhinolaryngology (01.12.2013)
Published in Brazilian journal of otorhinolaryngology (01.12.2013)
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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
de Moraes, Vanessa Cristine Sousa, dos Santos, Nathalia Zocal Pereira, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lúcia
Published in International journal of pediatric otorhinolaryngology (01.03.2013)
Published in International journal of pediatric otorhinolaryngology (01.03.2013)
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Differentiating Leber Hereditary Optic Neuropathy from Normal-Tension Glaucoma
Souto, Fernanda Maria Silveira, de Vasconcellos, José Paulo Cabral, de Melo, Mônica Barbosa, Sartorato, Edi Lúcia, Moura, Frederico Castelo
Published in Neuro-ophthalmology (Amsterdam : Aeolus Press. 1980) (04.03.2017)
Published in Neuro-ophthalmology (Amsterdam : Aeolus Press. 1980) (04.03.2017)
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Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy
Amaral-Fernandes, Marcela Scabello, Marcondes, Ana Maria, do Amor Divino Miranda, Paulo Maurício, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia
Published in Molecular vision (07.12.2011)
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Published in Molecular vision (07.12.2011)
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Genetic and audiologic study in elderly with sensorineural hearing loss
Martins, Kelly, Fontenele, Marília, Câmara, Silva, Sartorato, Edi Lúcia
Published in CoDAS (São Paulo) (2013)
Published in CoDAS (São Paulo) (2013)
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Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment
de Moraes, Vanessa Cristine Sousa, Alexandrino, Fabiana, Andrade, Paula Baloni, Câmara, Marília Fontenele, Sartorato, Edi Lúcia
Published in Biochemical and biophysical research communications (03.04.2009)
Published in Biochemical and biophysical research communications (03.04.2009)
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