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Haz muscular apicobasal del ventrículo izquierdo, ¿un marcador de miocardiopatía hipertrófica?
- Published in:
- Archivos de Cardiología de México, 2021, v. 91, n. 4, p. 512, doi. 10.24875/ACM.20000423
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- Publication type:
- Article
Bases genéticas y moleculares del síndrome de Brugada mediado por canales de sodio.
- Published in:
- Archivos de Cardiología de México, 2013, v. 83, n. 4, p. 295, doi. 10.1016/j.acmx.2013.10.001
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- Publication type:
- Article
The potential anti-arrhythmic effect of SGLT2 inhibitors.
- Published in:
- Cardiovascular Diabetology, 2024, v. 23, n. 1, p. 1, doi. 10.1186/s12933-024-02312-0
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- Article
Biophysical and molecular comparison of sodium current in cells isolated from canine atria and pulmonary vein.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2017, v. 469, n. 5/6, p. 703, doi. 10.1007/s00424-017-1956-4
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- Publication type:
- Article
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.
- Published in:
- 2022
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- Publication type:
- journal article
A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
- Published in:
- 2016
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- Publication type:
- journal article
LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.
- Published in:
- EP: Europace, 2011, v. 13, n. 10, p. 1478, doi. 10.1093/europace/eur184
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- Publication type:
- Article
Editorial: Arrhythmias in women.
- Published in:
- Frontiers in Cardiovascular Medicine, 2024, p. 1, doi. 10.3389/fcvm.2024.1348878
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- Publication type:
- Article
Novel polygenetic variants evidenced in a patient with Jervell and Lange-Nielsen syndrome.
- Published in:
- Cardiology Journal, 2021, v. 28, n. 5, p. 786, doi. 10.5603/CJ.a2021.0063
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- Publication type:
- Article
Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 7108, doi. 10.3390/ijms22137108
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- Publication type:
- Article
Dystrophin Deficiency Causes Progressive Depletion of Cardiovascular Progenitor Cells in the Heart.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 5025, doi. 10.3390/ijms22095025
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- Publication type:
- Article
T Wave Safety Margin during the Process of ICD Implantation As a Novel Predictor of T Wave Oversensing.
- Published in:
- Frontiers in Physiology, 2017, p. 1, doi. 10.3389/fphys.2017.00659
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- Publication type:
- Article
Comparative Effectiveness of Acupuncture and Antiarrhythmic Drugs for the Prevention of Cardiac Arrhythmias: A Systematic Review and Meta-analysis of Randomized Controlled Trials.
- Published in:
- Frontiers in Physiology, 2017, p. 1, doi. 10.3389/fphys.2017.00358
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- Publication type:
- Article
Mechanisms underlying the antiarrhythmic effect of ARumenamide-787 in experimental models of the J wave syndromes and hypothermia.
- Published in:
- PLoS ONE, 2023, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0281977
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- Publication type:
- Article
A temporal window of vulnerability for development of atrial fibrillation with advancing heart failure.
- Published in:
- European Journal of Heart Failure, 2014, v. 16, n. 3, p. 271, doi. 10.1002/ejhf.28
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- Publication type:
- Article
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes.
- Published in:
- Stem Cells International, 2020, p. 1, doi. 10.1155/2020/8842398
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- Publication type:
- Article
A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased Ca<sub>V</sub>1.2 Channel Window Current, and Arrhythmogenesis.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106982
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- Publication type:
- Article
Identification of a Novel <i>De Novo</i> Mutation Associated with <i>PRKAG2</i> Cardiac Syndrome and Early Onset of Heart Failure
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064603
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- Publication type:
- Article
Maximum Diastolic Potential of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Depends Critically on I<sub>Kr</sub>.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040288
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- Publication type:
- Article
TBX18 gene induces adipose-derived stem cells to differentiate into pacemaker-like cells in the myocardial microenvironment.
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- International Journal of Molecular Medicine, 2016, v. 38, n. 5, p. 1403, doi. 10.3892/ijmm.2016.2736
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- Publication type:
- Article
Hypertension as a sequela in patients of SARS-CoV-2 infection.
- Published in:
- PLoS ONE, 2021, v. 16, n. 4, p. 1, doi. 10.1371/journal.pone.0250815
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- Publication type:
- Article
Acacetin suppresses the electrocardiographic and arrhythmic manifestations of the J wave syndromes.
- Published in:
- PLoS ONE, 2020, v. 15, n. 11, p. 1, doi. 10.1371/journal.pone.0242747
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- Publication type:
- Article
Genetics Bases of Cardiac Sodium Channel Mutations linked to Inherited Cardiac Arrhythmias.
- Published in:
- 2016
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- Publication type:
- Editorial
Ionic and Cellular Mechanisms Underlying the Development of Acquired Brugada Syndrome in Patients Treated with Antidepressants.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2012, v. 23, n. 4, p. 423, doi. 10.1111/j.1540-8167.2011.02196.x
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- Publication type:
- Article
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.
- Published in:
- Journal of Arrhythmia, 2022, v. 38, n. 4, p. 491, doi. 10.1002/joa3.12717
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- Publication type:
- Article
A carvedilol analogue, VK‐II‐86, prevents hypokalaemia‐induced ventricular arrhythmia through novel multi‐channel effects.
- Published in:
- British Journal of Pharmacology, 2022, v. 179, n. 11, p. 2713, doi. 10.1111/bph.15775
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- Publication type:
- Article
Electrophysiologic Characteristics and Pharmacologic Response of Human Cardiomyocytes Isolated from a Patient with Hypertrophic Cardiomyopathy.
- Published in:
- Pacing & Clinical Electrophysiology, 2013, v. 36, n. 12, p. 1512, doi. 10.1111/pace.12227
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- Publication type:
- Article
Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome.
- Published in:
- Pacing & Clinical Electrophysiology, 2010, v. 33, n. 3, p. 274, doi. 10.1111/j.1540-8159.2009.02642.x
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- Publication type:
- Article
Larger dispersion of I<sub>Na</sub> in female dog ventricle as a mechanism for gender-specific incidence of cardiac arrhythmias.
- Published in:
- Cardiovascular Research, 2009, v. 81, n. 1, p. 82, doi. 10.1093/cvr/cvn255
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- Publication type:
- Article
SCN5A Genetic Polymorphisms Associated With Increased Defibrillator Shocks in Brugada Syndrome.
- Published in:
- Journal of the American Heart Association, 2017, v. 6, n. 6, p. 1, doi. 10.1161/JAHA.116.005009
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- Publication type:
- Article
Neuronal Na<sub>v</sub>1.8 Channels as a Novel Therapeutic Target of Acute Atrial Fibrillation Prevention.
- Published in:
- Journal of the American Heart Association, 2016, v. 5, n. 11, p. 1, doi. 10.1161/JAHA.116.004050
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- Article
Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.
- Published in:
- 2016
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- Publication type:
- journal article
Common variants in SCN10A gene associated with Brugada syndrome.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 2, p. 157, doi. 10.1093/hmg/ddab217
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- Publication type:
- Article
Meta-Analysis of Risk Stratification of SCN5A With Brugada Syndrome: Is SCN5A Always a Marker of Low Risk?
- Published in:
- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00103
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- Publication type:
- Article
Pooled Analysis of Risk Stratification of Spontaneous Type 1 Brugada ECG: Focus on the Influence of Gender and EPS.
- Published in:
- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2018.01951
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- Publication type:
- Article
Gender Differences in Prognosis and Risk Stratification of Brugada Syndrome: A Pooled Analysis of 4,140 Patients From 24 Clinical Trials.
- Published in:
- Frontiers in Physiology, 2018, p. N.PAG, doi. 10.3389/fphys.2018.01127
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- Publication type:
- Article
Acquired short QT syndrome in a cancer patient treated with Toad.
- Published in:
- Pacing & Clinical Electrophysiology, 2019, v. 42, n. 9, p. 1273, doi. 10.1111/pace.13708
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- Publication type:
- Article
Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.
- Published in:
- Congenital Heart Disease, 2016, v. 11, n. 6, p. 683, doi. 10.1111/chd.12371
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- Publication type:
- Article
Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6).
- Published in:
- European Heart Journal, 2011, v. 32, n. 9, p. 1077, doi. 10.1093/eurheartj/ehr076
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- Publication type:
- Article
Role of multimodality imaging in a patient with posterior left ventricular aneurysm and non-compaction: Review of the literature.
- Published in:
- Journal of Nuclear Cardiology, 2022, v. 29, n. 3, p. 1091, doi. 10.1007/s12350-020-02365-0
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- Publication type:
- Article
Rings and ovoid heart: OCIR. A new cardiomyopathy? Family genetic findings and multimodality imaging analysis. A rare cardiac phenotype and review of the literature.
- Published in:
- 2021
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- Publication type:
- journal article
Erratum to: Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome.
- Published in:
- 2017
- By:
- Publication type:
- journal article