Detalhe da pesquisa
1.
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical management.
Hum Mutat;
43(9): 1333-1342, 2022 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35819174
2.
Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse: Relation to Mitral Regurgitation, Ventricular Remodeling, and Arrhythmia.
Circulation;
143(18): 1763-1774, 2021 05 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33706538
3.
Robustness and relevance of predictive score in sudden cardiac death for patients with Brugada syndrome.
Eur Heart J;
42(17): 1687-1695, 2021 05 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33289793
4.
Mental stress test: a rapid, simple, and efficient test to unmask long QT syndrome.
Europace;
20(12): 2014-2020, 2018 12 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29688407
5.
CDK10/cyclin M is a protein kinase that controls ETS2 degradation and is deficient in STAR syndrome.
Proc Natl Acad Sci U S A;
110(48): 19525-30, 2013 Nov 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24218572
6.
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.
Nat Commun;
15(1): 3380, 2024 Apr 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38643172
7.
Outcome of patients with early repolarization pattern and syncope.
Heart Rhythm;
19(8): 1306-1314, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35395407
8.
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Nat Genet;
54(3): 232-239, 2022 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35210625
9.
Dose response to nadolol in congenital long QT syndrome.
Heart Rhythm;
18(8): 1377-1383, 2021 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33905813
10.
ZNF217 confers resistance to the pro-apoptotic signals of paclitaxel and aberrant expression of Aurora-A in breast cancer cells.
Mol Cancer;
9: 291, 2010 Nov 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21059223
11.
Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies.
ESC Heart Fail;
7(4): 1520-1533, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32356610
12.
Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmia.
Heart Rhythm;
17(5 Pt A): 743-749, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31790831
13.
Number of electrocardiogram leads in the diagnosis of spontaneous Brugada syndrome.
Arch Cardiovasc Dis;
113(3): 152-158, 2020 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31787523
14.
Clinical presentation and follow-up of women affected by Brugada syndrome.
Heart Rhythm;
16(2): 260-267, 2019 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30193851
15.
Brugada syndrome: Diagnosis, risk stratification and management.
Arch Cardiovasc Dis;
110(3): 188-195, 2017 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28139454
16.
Clinical Yield of Familial Screening After Sudden Death in Young Subjects: The French Experience.
Circ Arrhythm Electrophysiol;
10(9)2017 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28912206
17.
18F-Fluorodeoxyglucose Positron Emission Tomography for the Detection of Myocardial Inflammation in Arrhythmogenic Left Ventricular Cardiomyopathy.
Circ Cardiovasc Imaging;
15(7): e014065, 2022 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35770631
18.
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity.
Heart Rhythm;
14(10): 1442-1448, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28666944
19.
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.
J Am Coll Cardiol;
70(3): 358-370, 2017 Jul 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28705318
20.
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Nat Genet;
54(5): 735, 2022 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35474365