Detalhe da pesquisa
1.
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation
; 142(4): 324-338, 2020 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32429735
2.
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition.
Circulation
; 141(6): 429-439, 2020 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31941373
3.
Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).
Europace
; 21(5): 796-802, 2019 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30590530
4.
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
Eur Heart J
; 39(31): 2879-2887, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30059973
5.
A platelet P-selectin test predicts adverse cardiovascular events in patients with acute coronary syndromes treated with aspirin and clopidogrel.
Platelets
; 25(8): 612-8, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24433232
6.
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
7.
The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.
Eur J Hum Genet
; 28(1): 17-22, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31534214
8.
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families.
Circ Genom Precis Med
; 13(6): e002911, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33164571
9.
Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome.
J Am Coll Cardiol
; 73(14): 1756-1765, 2019 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30975291
10.
Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome.
Heart Rhythm
; 16(10): 1468-1474, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31284050
11.
Detection of P2Y(14) protein in platelets and investigation of the role of P2Y(14) in platelet function in comparison with the EP(3) receptor.
Thromb Haemost
; 100(2): 261-70, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18690346
12.
Characteristics of Patients with Spontaneous Versus Drug-Induced Brugada Electrocardiogram: Sub-Analysis From the SABRUS.
Circ Arrhythm Electrophysiol
; 16(1): e011360, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36595628
13.
Fever-related arrhythmic events in the multicenter Survey on Arrhythmic Events in Brugada Syndrome.
Heart Rhythm
; 15(9): 1394-1401, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29649615
14.
Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients.
Heart Rhythm
; 15(10): 1457-1465, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29908370
15.
Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).
Heart Rhythm
; 15(5): 716-724, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29325976
16.
Sudden death and cardiac arrest without phenotype: the utility of genetic testing.
Trends Cardiovasc Med
; 27(3): 207-213, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27692676
17.
Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?
Heart Rhythm
; 14(4): 583-589, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27919765
18.
Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients.
Circ Arrhythm Electrophysiol
; 10(12)2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29254945
19.
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.
J Am Coll Cardiol
; 69(17): 2134-2145, 2017 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28449774
20.
Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?
Circ Arrhythm Electrophysiol
; 10(8)2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28794082