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1.
Expression of Hv1 proton channels in myeloid-derived suppressor cells (MDSC) and its potential role in T cell regulation.
Proc Natl Acad Sci U S A
; 119(15): e2104453119, 2022 04 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35377790
2.
Common variants in SCN10A gene associated with Brugada syndrome.
Hum Mol Genet
; 31(2): 157-165, 2021 12 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-34312669
3.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-32893267
4.
Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Int J Mol Sci
; 22(13)2021 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34281161
5.
The Small Conductance Calcium-Activated Potassium Channel Inhibitors NS8593 and UCL1684 Prevent the Development of Atrial Fibrillation Through Atrial-Selective Inhibition of Sodium Channel Activity.
J Cardiovasc Pharmacol
; 76(2): 164-172, 2020 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-32453071
6.
Acquired short QT syndrome in a cancer patient treated with Toad.
Pacing Clin Electrophysiol
; 42(9): 1273-1275, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31037741
7.
A novel three base-pair deletion in domain two of the cardiac sodium channel causes Brugada syndrome.
J Electrocardiol
; 51(4): 667-673, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29997009
8.
Biophysical and molecular comparison of sodium current in cells isolated from canine atria and pulmonary vein.
Pflugers Arch
; 469(5-6): 703-712, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28243733
9.
Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome.
J Transl Med
; 15(1): 78, 2017 04 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-28427417
10.
Role of multimodality imaging in a patient with posterior left ventricular aneurysm and non-compaction: Review of the literature.
J Nucl Cardiol
; 29(3): 1091-1099, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33034035
11.
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.
Europace
; 24(8): 1307-1367, 2022 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35373836
12.
Rings and ovoid heart: OCIR. A new cardiomyopathy? Family genetic findings and multimodality imaging analysis. A rare cardiac phenotype and review of the literature.
J Nucl Cardiol
; 28(1): 359-366, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31897995
13.
A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
Europace
; 18(6): 897-904, 2016 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25829473
14.
Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome.
J Mol Cell Cardiol
; 68: 20-8, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24378566
15.
Gene and stem cell therapy for inherited cardiac arrhythmias.
Pharmacol Ther
; 256: 108596, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38301770
16.
Underlying mechanism of atrial fibrillation-associated Nppa-I137T mutation and cardiac effect of potential drug therapy.
Heart Rhythm
; 21(2): 184-196, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-37924963
17.
Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.
Circulation
; 125(1): 14-22, 2012 Jan 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-22090166
18.
Electrophysiologic characteristics and pharmacologic response of human cardiomyocytes isolated from a patient with hypertrophic cardiomyopathy.
Pacing Clin Electrophysiol
; 36(12): 1512-5, 2013 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-24117780
19.
Functional identification of hot-spot mutations in cardiac calcium channel genes associated with the J wave syndromes.
Philos Trans R Soc Lond B Biol Sci
; 378(1879): 20220286, 2023 06 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-37122210
20.
Mechanisms underlying the antiarrhythmic effect of ARumenamide-787 in experimental models of the J wave syndromes and hypothermia.
PLoS One
; 18(5): e0281977, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37159454