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Year Number of Results
2019 2
2020 1
2021 7
2022 1
2024 0

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11 results

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Page 1
Brugada Syndrome: Warning of a Systemic Condition?
D'Imperio S, Monasky MM, Micaglio E, Ciconte G, Anastasia L, Pappone C. D'Imperio S, et al. Front Cardiovasc Med. 2021 Oct 15;8:771349. doi: 10.3389/fcvm.2021.771349. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34722688 Free PMC article. Review.
The antithetic role of ceramide and sphingosine-1-phosphate in cardiac dysfunction.
Cirillo F, Piccoli M, Ghiroldi A, Monasky MM, Rota P, La Rocca P, Tarantino A, D'Imperio S, Signorelli P, Pappone C, Anastasia L. Cirillo F, et al. Among authors: d imperio s. J Cell Physiol. 2021 Jul;236(7):4857-4873. doi: 10.1002/jcp.30235. Epub 2021 Jan 11. J Cell Physiol. 2021. PMID: 33432663 Review.
Alterations of the Sialylation Machinery in Brugada Syndrome.
Ghiroldi A, Ciconte G, Creo P, Tarantino A, Melgari D, D'Imperio S, Piccoli M, Cirillo F, Micaglio E, Monasky MM, Frosio A, Locati ET, Vicedomini G, Rivolta I, Pappone C, Anastasia L. Ghiroldi A, et al. Among authors: d imperio s. Int J Mol Sci. 2022 Oct 29;23(21):13154. doi: 10.3390/ijms232113154. Int J Mol Sci. 2022. PMID: 36361941 Free PMC article.
Brugada syndrome genetics is associated with phenotype severity.
Ciconte G, Monasky MM, Santinelli V, Micaglio E, Vicedomini G, Anastasia L, Negro G, Borrelli V, Giannelli L, Santini F, de Innocentiis C, Rondine R, Locati ET, Bernardini A, Mazza BC, Mecarocci V, Ćalović Ž, Ghiroldi A, D'Imperio S, Benedetti S, Di Resta C, Rivolta I, Casari G, Petretto E, Pappone C. Ciconte G, et al. Among authors: d imperio s. Eur Heart J. 2021 Mar 14;42(11):1082-1090. doi: 10.1093/eurheartj/ehaa942. Eur Heart J. 2021. PMID: 33221895 Free PMC article.
Role of sialidase Neu3 and ganglioside GM3 in cardiac fibroblasts activation.
Ghiroldi A, Piccoli M, Creo P, Cirillo F, Rota P, D'Imperio S, Ciconte G, Monasky MM, Micaglio E, Garatti A, Aureli M, Carsana EV, Menicanti L, Pappone C, Anastasia L. Ghiroldi A, et al. Among authors: d imperio s. Biochem J. 2020 Sep 18;477(17):3401-3415. doi: 10.1042/BCJ20200360. Biochem J. 2020. PMID: 32869836 Free 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: d imperio s. Europace. 2019 Oct 1;21(10):1550-1558. doi: 10.1093/europace/euz186. Europace. 2019. PMID: 31292628
Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.
Monasky MM, Micaglio E, Ciconte G, Rivolta I, Borrelli V, Ghiroldi A, D'Imperio S, Binda A, Melgari D, Benedetti S, Mitrovic P, Anastasia L, Mecarocci V, Ćalović Ž, Casari G, Pappone C. Monasky MM, et al. Among authors: d imperio s. Int J Mol Sci. 2021 Apr 29;22(9):4700. doi: 10.3390/ijms22094700. Int J Mol Sci. 2021. PMID: 33946750 Free PMC article.
11 results