Detalhe da pesquisa
1.
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
2.
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
3.
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Acta Cardiol
; 74(1): 53-58, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29513133
4.
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Hum Mol Genet
; 21(9): 2039-53, 2012 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22286171
5.
Decision Support System Detecting Patients at Risk of Prolonged QT and Associated Mortality.
Stud Health Technol Inform
; 310: 1378-1379, 2024 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38269655
6.
Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapse.
Int J Cardiol
; 274: 175-178, 2019 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30219255