Výsledky vyhledávání - Franzè, Annamaria

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  1. 1
    GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss.

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

    Vydáno 2011
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  2. 2
    X-Linked Sensorineural Hearing Loss: A Literature Review

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

    Vydáno 2018
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  3. 3
    Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage?

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

    Vydáno 2015
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  4. 4
    Integrated Bimodal Fitting for Unilateral CI Users with Residual Contralateral Hearing

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

    Vydáno 2021
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  5. 5
    Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population

    Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population Autor 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

    Vydáno 2014
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  6. 6
    Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019

    Performance and characteristics of the Newborn Hearing Screening Program in Campania region (Italy) between 2013 and 2019 Autor 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

    Vydáno 2021
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  7. 7
    Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection

    Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection Autor 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

    Vydáno 2018
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  8. 8
    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

    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 Autor 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

    Vydáno 2022
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  9. 9
    Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss

    Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss Autor 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

    Vydáno 2018
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  10. 10
    Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants

    Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic s... Autor 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

    Vydáno 2017
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  11. 11
    Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss

    Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss Autor 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

    Vydáno 2015
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