Detalhe da pesquisa
1.
Reduced Ejection Fraction in Elite Endurance Athletes: Clinical and Genetic Overlap With Dilated Cardiomyopathy.
Circulation
; 149(18): 1405-1415, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38109351
2.
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
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.
Effectiveness of the risk stratification proposed by the 2022 European Heart Rhythm Association Expert Consensus statement on arrhythmic mitral valve prolapse.
Am Heart J
; 266: 48-60, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595658
6.
Importance of exercise stress testing in evaluation of unexplained cardiac arrest survivor.
Neth Heart J
; 31(11): 444-451, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37347419
7.
A deep learning approach identifies new ECG features in congenital long QT syndrome.
BMC Med
; 20(1): 162, 2022 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35501785
8.
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
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.
Clinical characterization of the first Belgian SCN5A founder mutation cohort.
Europace
; 23(6): 918-927, 2021 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33221854
11.
Quality of life outcomes in cryoablation of atrial fibrillation-A literature review.
Pacing Clin Electrophysiol
; 44(10): 1756-1768, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34406664
12.
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
13.
Combining noninvasive risk stratification parameters improves the prediction of mortality and appropriate ICD shocks.
Ann Noninvasive Electrocardiol
; 24(1): e12604, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30265438
14.
QT correction across the heart rate spectrum, in atrial fibrillation and ventricular conduction defects.
Pacing Clin Electrophysiol
; 41(9): 1101-1108, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29928779
15.
Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers.
Ann Noninvasive Electrocardiol
; 23(5): e12548, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29709101
16.
Prognostic value of electrocardiographic time intervals and QT rate dependence in hypertrophic cardiomyopathy.
J Electrocardiol
; 51(6): 1077-1083, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30497734
17.
Inter- and intra-observer variability of visual fragmented QRS scoring in ischemic and non-ischemic cardiomyopathy.
J Electrocardiol
; 51(3): 549-554, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29275955
18.
The impact of changes in LVEF and renal function on the prognosis of ICD patients after elective device replacement.
Pacing Clin Electrophysiol
; 40(10): 1147-1159, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28857211
19.
Evaluation of Index of Cardio-Electrophysiological Balance (iCEB) as a New Biomarker for the Identification of Patients at Increased Arrhythmic Risk.
Ann Noninvasive Electrocardiol
; 21(3): 294-304, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26305685
20.
Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout.
Acta Cardiol
; 70(6): 747-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26717233