檢索結果 - Franzè, Annamaria

GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss. 由 Iossa, Sandra, Marciano, Elio, Franzé, Annamaria

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X-Linked Sensorineural Hearing Loss: A Literature Review 由 Corvino, Virginia, Apisa, Pasqualina, Malesci, Rita, Laria, Carla, Auletta, Gennaro, Franzé, Annamaria

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Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage? 由 Vuckovic, Dragana, Dallapiccola, Bruno, Franzè, Annamaria, Mauri, Lucia, Perrone, Maria Dolores, Gasparini, Paolo

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Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing 由 Auletta, Gennaro, Franzè, Annamaria, Laria, Carla, Piccolo, Carmine, Papa, Carmine, Riccardi, Pasquale, Pisani, Davide, Sarnelli, Angelo, Del Vecchio, Valeria, Malesci, Rita, Marciano, Elio

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Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population 由 Iossa, Sandra, Morello, Giovanna, Esposito, Teresa, Corvino, Virginia, Giannini, Pasquale, Salvato, Raffaella, Cavaliere, Michele, Panetti, Maria, Panetti, Giuseppe, Piantedosi, Bruno, Gianfrancesco, Fernando, Marciano, Elio, Franzè, Annamaria

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Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019 由 Malesci, Rita, Del Vecchio, Valeria, Bruzzese, Dario, Burattini, Ernesto, Auletta, Gennaro, Errichiello, Monica, Fetoni, Anna Rita, Franzè, Annamaria, Laria, Carla, Toscano, Fabiana, Caso, Antonio, Marciano, Elio

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Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 由 Vuckovic, Dragana, Mezzavilla, Massimo, Cocca, Massimiliano, Morgan, Anna, Brumat, Marco, Catamo, Eulalia, Concas, Maria Pina, Biino, Ginevra, Franzè, Annamaria, Ambrosetti, Umberto, Pirastu, Mario, Gasparini, Paolo, Girotto, Giorgia

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NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing Loss 由 Landolfi, Emma, Continisio, Grazia Isabella, Del Vecchio, Valeria, Serra, Nicola, Burattini, Ernesto, Conson, Massimiliano, Marciano, Elio, Laria, Carla, Franzè, Annamaria, Caso, Antonio, Fetoni, Anna Rita, Malesci, Rita

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Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 由 Morgan, Anna, Vuckovic, Dragana, Krishnamoorthy, Navaneethakrishnan, Rubinato, Elisa, Ambrosetti, Umberto, Castorina, Pierangela, Franzè, Annamaria, Vozzi, Diego, La Bianca, Martina, Cappellani, Stefania, Di Stazio, Mariateresa, Gasparini, Paolo, Girotto, Giorgia

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Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic s... 由 Esposito, Gabriella, Testa, Francesco, Zacchia, Miriam, Crispo, Anna Alessia, Di Iorio, Valentina, Capolongo, Giovanna, Rinaldi, Luca, D’Antonio, Marcella, Fioretti, Tiziana, Iadicicco, Pasquale, Rossi, Settimio, Franzè, Annamaria, Marciano, Elio, Capasso, Giovanbattista, Simonelli, Francesca, Salvatore, Francesco

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Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 由 Iossa, Sandra, Costa, Valerio, Corvino, Virginia, Auletta, Gennaro, Barruffo, Luigi, Cappellani, Stefania, Ceglia, Carlo, Cennamo, Giovanni, D’Adamo, Adamo Pio, D’Amico, Alessandra, Di Paolo, Nilde, Forte, Raimondo, Gasparini, Paolo, Laria, Carla, Lombardo, Barbara, Malesci, Rita, Vitale, Andrea, Marciano, Elio, Franzè, Annamaria

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