Detalhe da pesquisa
1.
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
2.
Percutaneous left atrial appendage occlusion: impact on left atrial deformation indices.
Int J Cardiovasc Imaging
; 39(2): 359-367, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322264
3.
Renal denervation prevents subclinical atrial fibrillation in patients with hypertensive heart disease: Randomized, sham-controlled trial.
Heart Rhythm
; 19(11): 1765-1773, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35781044
4.
Who are the long-QT syndrome patients who receive an implantable cardioverter-defibrillator and what happens to them?: data from the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry.
Circulation
; 122(13): 1272-82, 2010 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-20837891
5.
NOS1AP is a genetic modifier of the long-QT syndrome.
Circulation
; 120(17): 1657-63, 2009 Oct 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-19822806
6.
The genetic basis of long QT and short QT syndromes: a mutation update.
Hum Mutat
; 30(11): 1486-511, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19862833
7.
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.
Cardiovasc Res
; 77(4): 687-94, 2008 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18029407
8.
Renal Denervation in High-risk Patients with Hypertension.
Heart Int
; 13(2): 12-16, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-36274824
9.
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population.
Stem Cell Res
; 39: 101510, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31398660
10.
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene.
Stem Cell Res
; 36: 101416, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30878014
11.
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.
Circulation
; 116(21): 2366-75, 2007 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-17984373
12.
Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy.
Hum Genet
; 124(1): 57-61, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18560893
13.
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.
Circulation
; 112(17): 2602-10, 2005 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-16246960
14.
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?
Circ Cardiovasc Genet
; 9(4): 330-9, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27531917
15.
Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome.
Circulation
; 109(15): 1826-33, 2004 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-15051644
16.
Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.
Cardiovasc J Afr
; 26(2): 63-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25940119
17.
Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients.
Annu Int Conf IEEE Eng Med Biol Soc
; 2015: 294-7, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26736258
18.
Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1.
J Am Coll Cardiol
; 65(4): 367-374, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25634836
19.
Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population.
Int J Neuropsychopharmacol
; 3(4): 327-331, 2000 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11343612
20.
Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population.
Annu Int Conf IEEE Eng Med Biol Soc
; 2014: 6671-4, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25571526