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Brugada Syndrome: Oligogenic or Mendelian Disease?
Monasky MM, Micaglio E, Ciconte G, Pappone C. Monasky MM, et al. Among authors: micaglio e. Int J Mol Sci. 2020 Mar 1;21(5):1687. doi: 10.3390/ijms21051687. Int J Mol Sci. 2020. PMID: 32121523 Free PMC article. Review.
Calcium in Brugada Syndrome: Questions for Future Research.
Monasky MM, Pappone C, Piccoli M, Ghiroldi A, Micaglio E, Anastasia L. Monasky MM, et al. Among authors: micaglio e. Front Physiol. 2018 Aug 10;9:1088. doi: 10.3389/fphys.2018.01088. eCollection 2018. Front Physiol. 2018. PMID: 30147658 Free PMC article. Review.
SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis.
Micaglio E, Monasky MM, Ciconte G, Vicedomini G, Conti M, Mecarocci V, Giannelli L, Giordano F, Pollina A, Saviano M, Crisà S, Borrelli V, Ghiroldi A, D'Imperio S, Di Resta C, Benedetti S, Ferrari M, Santinelli V, Anastasia L, Pappone C. Micaglio E, et al. Front Genet. 2019 Feb 15;10:50. doi: 10.3389/fgene.2019.00050. eCollection 2019. Front Genet. 2019. PMID: 30828344 Free PMC article.
Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene.
Monasky MM, Micaglio E, Ciconte G, Benedetti S, Di Resta C, Vicedomini G, Borrelli V, Ghiroldi A, Piccoli M, Anastasia L, Santinelli V, Ferrari M, Pappone C. Monasky MM, et al. Among authors: micaglio e. Front Physiol. 2019 May 28;10:666. doi: 10.3389/fphys.2019.00666. eCollection 2019. Front Physiol. 2019. PMID: 31191357 Free PMC article.
Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.
Monasky MM, Micaglio E, Vicedomini G, Locati ET, Ciconte G, Giannelli L, Giordano F, Crisà S, Vecchi M, Borrelli V, Ghiroldi A, D'Imperio S, Di Resta C, Benedetti S, Ferrari M, Santinelli V, Anastasia L, Pappone C. Monasky MM, et al. Among authors: micaglio e. Europace. 2019 Oct 1;21(10):1550-1558. doi: 10.1093/europace/euz186. Europace. 2019. PMID: 31292628
Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome.
Micaglio E, Monasky MM, Resta N, Bagnulo R, Ciconte G, Giannelli L, Locati ET, Vicedomini G, Borrelli V, Ghiroldi A, Anastasia L, Benedetti S, Di Resta C, Ferrari M, Pappone C. Micaglio E, et al. Int J Mol Sci. 2019 Oct 4;20(19):4920. doi: 10.3390/ijms20194920. Int J Mol Sci. 2019. PMID: 31590245 Free PMC article.
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 MM, Micaglio E, Giannelli L, Negro G, Giordano F, Mecarocci V, Mazza BC, Locati E, Anastasia L, Calovic Z, Pappone C. Ciconte G, et al. Among authors: micaglio e. Europace. 2019 Dec 1;21(12):1900-1910. doi: 10.1093/europace/euz295. Europace. 2019. PMID: 31647530
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 MM, Lombardi M, Calovic Z, Santinelli V. Pappone C, et al. Among authors: micaglio e. Heart Rhythm. 2020 Apr;17(4):637-645. doi: 10.1016/j.hrthm.2019.11.019. Epub 2019 Nov 19. Heart Rhythm. 2020. PMID: 31756528 Free article.
53 results