Hasil Pencarian - Umberto Ambrosetti

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  1. 1
    TAS2R38 Genotype Does Not Affect SARS-CoV-2 Infection in Primary Ciliary Dyskinesia

    TAS2R38 Genotype Does Not Affect SARS-CoV-2 Infection in Primary Ciliary Dyskinesia oleh Gioia Piatti, Giorgia Girotto, Maria Pina Concas, Leonardo Braga, Umberto Ambrosetti, Mirko Aldè

    Diterbitkan 2024-08-01
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  2. 2
    Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss

    Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss oleh Chiara Chiereghin, Michela Robusto, Valentina Massa, Pierangela Castorina, Umberto Ambrosetti, Rosanna Asselta, Giulia Soldà

    Diterbitkan 2022-05-01
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  3. 3
    Psychometric properties of the Italian Tinnitus Functional Index (TFI)

    Psychometric properties of the Italian Tinnitus Functional Index (TFI) oleh Stefania Barozzi, Luca Del Bo, Silvia Passoni, Daniela Ginocchio, Luca Negri, Andrea Crocetti, Umberto Ambrosetti

    Diterbitkan 2020-06-01
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  4. 4
    Unilateral Sensorineural Hearing Loss in Children: Etiology, Audiological Characteristics, and Treatment

    Unilateral Sensorineural Hearing Loss in Children: Etiology, Audiological Characteristics, and Treatment oleh Mirko Aldè, Diego Zanetti, Umberto Ambrosetti, Eleonora Monaco, Anna Maria Gasbarre, Lorenzo Pignataro, Giovanna Cantarella, Stefania Barozzi

    Diterbitkan 2024-03-01
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  5. 5
    Diagnosis of congenital CMV infection via DBS samples testing and neonatal hearing screening: an observational study in Italy

    Diagnosis of congenital CMV infection via DBS samples testing and neonatal hearing screening: an observational study in Italy oleh Laura Pellegrinelli, Cristina Galli, Valeria Primache, Mirko Alde’, Enrico Fagnani, Federica Di Berardino, Diego Zanetti, Elena Pariani, Umberto Ambrosetti, Sandro Binda

    Diterbitkan 2019-07-01
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  6. 6
    SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa

    SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa oleh Chiara Chiereghin, Michela Robusto, Lucia Mauri, Paola Primignani, Pierangela Castorina, Umberto Ambrosetti, Stefano Duga, Stefano Duga, Rosanna Asselta, Rosanna Asselta, Giulia Soldà, Giulia Soldà

    Diterbitkan 2021-02-01
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  7. 7
    In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear.

    In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear. oleh Chiara Chiereghin, Michela Robusto, Morag A Lewis, Susana Caetano, Valentina Massa, Pierangela Castorina, Umberto Ambrosetti, Karen P Steel, Stefano Duga, Rosanna Asselta, Giulia Soldà

    Diterbitkan 2023-01-01
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  8. 8
    Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations

    Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy N... oleh Anna Morgan, Stefania Lenarduzzi, Stefania Cappellani, Vanna Pecile, Marcello Morgutti, Eva Orzan, Sara Ghiselli, Umberto Ambrosetti, Marco Brumat, Poornima Gajendrarao, Martina La Bianca, Flavio Faletra, Enrico Grosso, Fabio Sirchia, Alberto Sensi, Claudio Graziano, Marco Seri, Paolo Gasparini, Paolo Gasparini, Giorgia Girotto, Giorgia Girotto

    Diterbitkan 2018-12-01
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