Hasil Pencarian - Berardo Rinaldi

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  1. 1
    Correction to: Incidental finding of APC deletion in a child: double trouble or double chance? – a case report

    Correction to: Incidental finding of APC deletion in a child: double trouble or double chance? – a case report oleh Erica Rosina, Berardo Rinaldi, Rosamaria Silipigni, Luca Bergamaschi, Giovanna Gattuso, Stefano Signoroni, Silvana Guerneri, Alessandra Carnevali, Paola Giovanna Marchisio, Donatella Milani

    Diterbitkan 2021-09-01
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  2. 2
    Incidental finding of APC deletion in a child: double trouble or double chance? – a case report

    Incidental finding of APC deletion in a child: double trouble or double chance? – a case report oleh Erica Rosina, Berardo Rinaldi, Rosamaria Silipigni, Luca Bergamaschi, Giovanna Gattuso, Stefano Signoroni, Silvana Guerneri, Alessandra Carnevali, Paola Giovanna Marchisio, Donatella Milani

    Diterbitkan 2021-02-01
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  3. 3
    Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force

    Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force oleh Berardo Rinaldi, Alessandro Vaisfeld, Sergio Amarri, Chiara Baldo, Giuseppe Gobbi, Pamela Magini, Erto Melli, Giovanni Neri, Francesca Novara, Tommaso Pippucci, Romana Rizzi, Annarosa Soresina, Laura Zampini, Orsetta Zuffardi, Marco Crimi

    Diterbitkan 2017-04-01
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  4. 4
    Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literature

    Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literature oleh Irene Picciolli, Angelo Ratti, Berardo Rinaldi, Anwar Baban, Maria Iascone, Gaia Francescato, Alessia Cappelleri, Monia Magliozzi, Antonio Novelli, Giovanni Parlapiano, Anna Maria Colli, Nicola Persico, Stefano Carugo, Fabio Mosca, Maria Francesca Bedeschi

    Diterbitkan 2024-08-01
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  5. 5
    X-linked neonatal-onset epileptic encephalopathy associated with a gain-of-function variant p.R660T in GRIA3.

    X-linked neonatal-onset epileptic encephalopathy associated with a gain-of-function variant p.R660T in GRIA3. oleh Jia-Hui Sun, Jiang Chen, Fernando Eduardo Ayala Valenzuela, Carolyn Brown, Diane Masser-Frye, Marilyn Jones, Leslie Patron Romero, Berardo Rinaldi, Wenhui Laura Li, Qing-Qing Li, Dan Wu, Benedicte Gerard, Erin Thorpe, Allan Bayat, Yun Stone Shi

    Diterbitkan 2021-06-01
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