20182019

Research output per year

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Fingerprint Dive into the research topics where Valeria Borrelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants

Monasky, M. M., Micaglio, E., Vicedomini, G., Locati, E. T., Ciconte, G., Giannelli, L., Giordano, F., Crisà, S., Vecchi, M., Borrelli, V., Ghiroldi, A., D'Imperio, S., Resta, C. D., Benedetti, S., Ferrari, M., Santinelli, V., Anastasia, L. & Pappone, C., Oct 1 2019, In : Europace. 21, 10, p. 1550-1558 9 p.

Research output: Contribution to journalArticle

  • Genotype–phenotype correlation in a family with brugada syndrome harboring the novel p.Gln371* Nonsense variant in the scn5a gene

    Monasky, M. M., Micaglio, E., Giachino, D., Ciconte, G., Giannelli, L., Locati, E. T., Ramondini, E., Cotugno, R., Vicedomini, G., Borrelli, V., Ghiroldi, A., Anastasia, L. & Pappone, C., Nov 2019, In : International Journal of Molecular Sciences. 20, 22, 5522.

    Research output: Contribution to journalArticle

    Open Access
  • New electromechanical substrate abnormalities in high-risk patients with Brugada syndrome

    Pappone, C., Mecarocci, V., Manguso, F., Ciconte, G., Vicedomini, G., Sturla, F., Votta, E., Mazza, B., Pozzi, P., Borrelli, V., Anastasia, L., Micaglio, E., Locati, E., Monasky, M. M., Lombardi, M., Calovic, Z. & Santinelli, V., Nov 19 2019, In : Heart Rhythm.

    Research output: Contribution to journalArticle

  • Non-invasive assessment of the arrhythmogenic substrate in Brugada syndrome using signal-averaged electrocardiogram: Clinical implications from a prospective clinical trial

    Ciconte, G., Santinelli, V., Vicedomini, G., Borrelli, V., Monasky, M. M., Micaglio, E., Giannelli, L., Negro, G., Giordano, F., Mecarocci, V., Mazza, B. C., Locati, E., Anastasia, L., Calovic, Z. & Pappone, C., Dec 1 2019, In : Europace. 21, 12, p. 1900-1910 11 p.

    Research output: Contribution to journalArticle

  • Novel scn5a p.W697x nonsense mutation segregation in a family with brugada syndrome

    Micaglio, E., Monasky, M. M., Resta, N., Bagnulo, R., Ciconte, G., Gianelli, L., Locati, E. T., Vicedomini, G., Borrelli, V., Ghiroldi, A., Anastasia, L., Benedetti, S., Di Resta, C., Ferrari, M. & Pappone, C., Oct 1 2019, In : International Journal of Molecular Sciences. 20, 19, 4920.

    Research output: Contribution to journalArticle

    Open Access