Detalhe da pesquisa
1.
Brugada syndrome genetics is associated with phenotype severity.
Eur Heart J
; 42(11): 1082-1090, 2021 03 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33221895
2.
Alterations of the Sialylation Machinery in Brugada Syndrome.
Int J Mol Sci
; 23(21)2022 Oct 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36361941
3.
The antithetic role of ceramide and sphingosine-1-phosphate in cardiac dysfunction.
J Cell Physiol
; 236(7): 4857-4873, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432663
4.
Role of sialidase Neu3 and ganglioside GM3 in cardiac fibroblasts activation.
Biochem J
; 477(17): 3401-3415, 2020 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32869836
5.
Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel TTN Frameshift Mutation.
Int J Mol Sci
; 22(2)2021 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33445410
6.
Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.
Int J Mol Sci
; 22(9)2021 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33946750
7.
The omics of channelopathies and cardiomyopathies: what we know and how they are useful.
Eur Heart J Suppl
; 22(Suppl L): L105-L109, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33654474
8.
Right ventricular electromechanical abnormalities in Brugada syndrome: is this a cardiomyopathy?
Eur Heart J Suppl
; 22(Suppl E): E101-E104, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32523450
9.
Brugada Syndrome: Oligogenic or Mendelian Disease?
Int J Mol Sci
; 21(5)2020 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32121523
10.
Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome.
Int J Mol Sci
; 21(16)2020 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32824506
11.
Non-invasive assessment of the arrhythmogenic substrate in Brugada syndrome using signal-averaged electrocardiogram: clinical implications from a prospective clinical trial.
Europace
; 21(12): 1900-1910, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31647530
12.
Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.
Europace
; 21(10): 1550-1558, 2019 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31292628
13.
Epicardial ablation in genetic cardiomyopathies: a new frontier.
Eur Heart J Suppl
; 21(Suppl B): B61-B66, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30948952
14.
Novel JAG1 Deletion Variant in Patient with Atypical Alagille Syndrome.
Int J Mol Sci
; 20(24)2019 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31835735
15.
Genotype-Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371* Nonsense Variant in the SCN5A Gene.
Int J Mol Sci
; 20(22)2019 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31698696
16.
Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome.
Int J Mol Sci
; 20(19)2019 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31590245
17.
Cell-Based Therapies for Cardiac Regeneration: A Comprehensive Review of Past and Ongoing Strategies.
Int J Mol Sci
; 19(10)2018 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30332812
18.
Letter by Romani et al Regarding Article, "Extracellular Vesicles From Epicardial Fat Facilitate Atrial Fibrillation".
Circulation
; 144(18): e280-e281, 2021 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34723643
19.
Common modulators of Brugada syndrome phenotype do not affect SCN5A prognostic value.
Eur Heart J
; 42(13): 1273-1274, 2021 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33595071
20.
The C-terminus of the long AKAP13 isoform (AKAP-Lbc) is critical for development of compensatory cardiac hypertrophy.
J Mol Cell Cardiol
; 66: 27-40, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24161911