Detalhe da pesquisa
1.
Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation.
Eur Heart J
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38751064
2.
Implantable loop recorders in patients with Brugada syndrome: the BruLoop study.
Eur Heart J
; 45(14): 1255-1265, 2024 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38445836
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.
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
5.
Effects of cohort, genotype, variant, and maternal ß-blocker treatment on foetal heart rate predictors of inherited long QT syndrome.
Europace
; 25(11)2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37975542
6.
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
7.
Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome.
Circulation
; 142(25): 2405-2415, 2020 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33073610
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.
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
10.
Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk.
Am J Physiol Heart Circ Physiol
; 318(6): H1357-H1370, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32196358
11.
Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study.
Am J Obstet Gynecol
; 222(3): 263.e1-263.e11, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31520628
12.
Partial Pericardial Agenesis Mimicking Arrhythmogenic Right Ventricular Cardiomyopathy.
Clin J Sport Med
; 30(5): e159-e162, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30893123
13.
From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2.
Eur Heart J
; 40(23): 1832-1836, 2019 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30753398
14.
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.
Eur Heart J
; 40(35): 2964-2975, 2019 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31170290
15.
For neonatal ECG screening there is no reason to relinquish old Bazett's correction.
Eur Heart J
; 39(31): 2888-2895, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29860404
16.
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
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.
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
19.
Prognostic Value of Multiplexed Assays of Variant Effect and Automated Patch-clamping for KCNH2-LQTS Risk Stratification.
medRxiv
; 2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38370760
20.
Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for Management.
JACC Clin Electrophysiol
; 8(3): 281-294, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35331422