Works by Borrelli, Valeria


Results: 23
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    Brugada syndrome genetics is associated with phenotype severity.

    Published in:
    European Heart Journal, 2021, v. 42, n. 11, p. 1082, doi. 10.1093/eurheartj/ehaa942
    By:
    • Ciconte, Giuseppe;
    • Monasky, Michelle M;
    • Santinelli, Vincenzo;
    • Micaglio, Emanuele;
    • Vicedomini, Gabriele;
    • Anastasia, Luigi;
    • Negro, Gabriele;
    • Borrelli, Valeria;
    • Giannelli, Luigi;
    • Santini, Francesca;
    • Innocentiis, Carlo de;
    • Rondine, Roberto;
    • Locati, Emanuela T;
    • Bernardini, Andrea;
    • Mazza, Beniamino C;
    • Mecarocci, Valerio;
    • Ćalović, Žarko;
    • Ghiroldi, Andrea;
    • D'Imperio, Sara;
    • Benedetti, Sara
    Publication type:
    Article
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    Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4700, doi. 10.3390/ijms22094700
    By:
    • Monasky, Michelle M.;
    • Micaglio, Emanuele;
    • Ciconte, Giuseppe;
    • Rivolta, Ilaria;
    • Borrelli, Valeria;
    • Ghiroldi, Andrea;
    • D'Imperio, Sara;
    • Binda, Anna;
    • Melgari, Dario;
    • Benedetti, Sara;
    • Mitrovic, Predrag;
    • Anastasia, Luigi;
    • Mecarocci, Valerio;
    • Ćalović, Žarko;
    • Casari, Giorgio;
    • Pappone, Carlo;
    • Knöll, Ralph
    Publication type:
    Article
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    Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome.

    Published in:
    International Journal of Molecular Sciences, 2020, v. 21, n. 16, p. 5902, doi. 10.3390/ijms21165902
    By:
    • Monasky, Michelle M.;
    • Micaglio, Emanuele;
    • Ciconte, Giuseppe;
    • Borrelli, Valeria;
    • Giannelli, Luigi;
    • Vicedomini, Gabriele;
    • Ghiroldi, Andrea;
    • Anastasia, Luigi;
    • Locati, Emanuela T.;
    • Benedetti, Sara;
    • Di Resta, Chiara;
    • Casari, Giorgio;
    • Pappone, Carlo
    Publication type:
    Article
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    Genotype–Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371* Nonsense Variant in the SCN5A Gene.

    Published in:
    International Journal of Molecular Sciences, 2019, v. 20, n. 22, p. 5522, doi. 10.3390/ijms20225522
    By:
    • Monasky, Michelle M.;
    • Micaglio, Emanuele;
    • Giachino, Daniela;
    • Ciconte, Giuseppe;
    • Giannelli, Luigi;
    • Locati, Emanuela T.;
    • Ramondini, Elisa;
    • Cotugno, Roberta;
    • Vicedomini, Gabriele;
    • Borrelli, Valeria;
    • Ghiroldi, Andrea;
    • Anastasia, Luigi;
    • Pappone, Carlo
    Publication type:
    Article
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    Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome.

    Published in:
    International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4920, doi. 10.3390/ijms20194920
    By:
    • Micaglio, Emanuele;
    • Monasky, Michelle M.;
    • Resta, Nicoletta;
    • Bagnulo, Rosanna;
    • Ciconte, Giuseppe;
    • Gianelli, Luigi;
    • Locati, Emanuela T.;
    • Vicedomini, Gabriele;
    • Borrelli, Valeria;
    • Ghiroldi, Andrea;
    • Anastasia, Luigi;
    • Benedetti, Sara;
    • Di Resta, Chiara;
    • Ferrari, Maurizio;
    • Pappone, Carlo
    Publication type:
    Article