Detalhe da pesquisa
1.
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 148(25): 2029-2037, 2023 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37886885
2.
Insights into adherence to medication and lifestyle recommendations in an international cohort of patients with catecholaminergic polymorphic ventricular tachycardia.
Europace
; 26(2)2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38349347
3.
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.
Eur Heart J
; 44(35): 3357-3370, 2023 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37528649
4.
An International Multicenter Cohort Study on ß-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 145(5): 333-344, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34874747
5.
Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathies.
Genet Med
; 25(3): 100355, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36496179
6.
Heart rate variability in congenital central hypoventilation syndrome: relationships with hypertension and sinus pauses.
Pediatr Res
; 93(4): 1003-1009, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35882978
7.
Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region.
Eur Heart J
; 42(46): 4743-4755, 2021 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34505893
8.
Deep learning analysis of electrocardiogram for risk prediction of drug-induced arrhythmias and diagnosis of long QT syndrome.
Eur Heart J
; 42(38): 3948-3961, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34468739
9.
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 142(10): 932-947, 2020 09 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32693635
10.
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Genet Med
; 23(1): 47-58, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893267
11.
Computerized automated algorithm-based analyses of digitized paper ECGs in Brugada syndrome.
J Electrocardiol
; 69S: 61-66, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34563332
12.
Sex influences on ventricular repolarization duration in normal subjects and in type 1, 2 and 3 long QT syndrome patients: Different effect in acquired and congenital type 2 LQTS.
J Electrocardiol
; 62: 148-154, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32905894
13.
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest.
Eur Heart J
; 40(35): 2953-2961, 2019 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31145795
14.
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
15.
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
16.
Comparison of automated interval measurements by widely used algorithms in digital electrocardiographs.
Am Heart J
; 200: 1-10, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29898835
17.
The genetics underlying acquired long QT syndrome: impact for genetic screening.
Eur Heart J
; 37(18): 1456-64, 2016 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26715165
18.
A Common Mutation of Long QT Syndrome Type 1 in Japan.
Circ J
; 79(9): 2026-30, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26118460
19.
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.
Hum Mol Genet
; 21(12): 2759-67, 2012 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22422768
20.
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
Basic Res Cardiol
; 109(6): 446, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25341504