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.
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
3.
A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy.
Eur Heart J
; 39(31): 2898-2907, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29718149
4.
Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome.
Circ Res
; 115(4): 460-9, 2014 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24963029
5.
Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan.
Circ J
; 84(11): 2124-2126, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33100286
6.
Channelopathies - emerging trends in the management of inherited arrhythmias.
Indian Pacing Electrophysiol J
; 15(1): 43-54, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25852242
7.
Genetic and clinical advances in congenital long QT syndrome.
Circ J
; 78(12): 2827-33, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25274057
8.
Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan.
Circ J
; 77(7): 1705-13, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23595086
9.
Rationale and design of the PRAETORIAN trial: a Prospective, RAndomizEd comparison of subcuTaneOus and tRansvenous ImplANtable cardioverter-defibrillator therapy.
Am Heart J
; 163(5): 753-760.e2, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22607851
10.
Seasonal and circadian distributions of cardiac events in genotyped patients with congenital long QT syndrome.
Circ J
; 76(9): 2112-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22785222
11.
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
12.
Risk determinants in individuals with a spontaneous type 1 Brugada ECG.
Circ J
; 75(4): 844-51, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21343656
13.
Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands.
Circ Genom Precis Med
; 14(5): e003222, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34461752
14.
Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndrome.
Europace
; 12(11): 1623-9, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20880952
15.
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
16.
Characteristics of bundle branch reentrant ventricular tachycardia with a right bundle branch block configuration: feasibility of atrial pacing.
Europace
; 11(9): 1208-13, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19661115
17.
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
18.
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
19.
Can common-type atrial flutter be a sign of an arrhythmogenic substrate in paroxysmal atrial fibrillation? Clinical and ablative consequences in patients with coexistent paroxysmal atrial fibrillation/atrial flutter.
Circulation
; 116(24): 2786-92, 2007 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18040030
20.
Influence of meals on variations of ST segment elevation in patients with Brugada syndrome.
J Cardiovasc Electrophysiol
; 19(1): 62-8, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17900254