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Page 1
Cu(II) Binding Increases the Soluble Toxicity of Amyloidogenic Light Chains.
Russo R, Romeo M, Schulte T, Maritan M, Oberti L, Barzago MM, Barbiroli A, Pappone C, Anastasia L, Palladini G, Diomede L, Ricagno S. Russo R, et al. Among authors: pappone c. Int J Mol Sci. 2022 Jan 16;23(2):950. doi: 10.3390/ijms23020950. Int J Mol Sci. 2022. PMID: 35055136 Free PMC article.
Commentary: Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada Syndrome.
Monasky MM, Ciconte G, Anastasia L, Pappone C. Monasky MM, et al. Among authors: pappone c. Front Physiol. 2017 Dec 12;8:1056. doi: 10.3389/fphys.2017.01056. eCollection 2017. Front Physiol. 2017. PMID: 29311983 Free PMC article. No abstract available.
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: pappone c. Front Physiol. 2018 Aug 10;9:1088. doi: 10.3389/fphys.2018.01088. eCollection 2018. Front Physiol. 2018. PMID: 30147658 Free PMC article. Review.
GM1 Ganglioside Promotes Osteogenic Differentiation of Human Tendon Stem Cells.
Bergante S, Creo P, Piccoli M, Ghiroldi A, Menon A, Cirillo F, Rota P, Monasky MM, Ciconte G, Pappone C, Randelli P, Anastasia L. Bergante S, et al. Among authors: pappone c. Stem Cells Int. 2018 Aug 23;2018:4706943. doi: 10.1155/2018/4706943. eCollection 2018. Stem Cells Int. 2018. PMID: 30210549 Free PMC article.
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. Among authors: pappone c. 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: pappone c. 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: pappone c. Europace. 2019 Oct 1;21(10):1550-1558. doi: 10.1093/europace/euz186. Europace. 2019. PMID: 31292628
261 results