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Genetic testing in early-onset atrial fibrillation.
- Published in:
- European Heart Journal, 2024, v. 45, n. 34, p. 3111, doi. 10.1093/eurheartj/ehae298
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- Publication type:
- Article
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.
- Published in:
- Human Genetics, 2000, v. 106, n. 6, p. 614, doi. 10.1007/s004390000308
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- Publication type:
- Article
Is it safe to give birth with an activated implantable cardioverter–defibrillator: A multicentre observational study.
- Published in:
- BJOG: An International Journal of Obstetrics & Gynaecology, 2024, v. 131, n. 9, p. 1290, doi. 10.1111/1471-0528.17777
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- Publication type:
- Article
The genetic basis of ventricular arrhythmias in structurally normal hearts.
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- Journal of Practical Electrocardiology, 2019, v. 28, n. 3, p. 177, doi. 10.13308/j.issn.2095-9354.2019.03.005
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- Publication type:
- Article
遗传性原发性心律失常综合征患者的风险评估.
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- Journal of Practical Electrocardiology, 2018, v. 27, n. 3, p. 175, doi. 10.13308/j.issn.2095-9354.2018.03.004
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- Publication type:
- Article
Risk stratification of patients with primary arrhythmia syndrome.
- Published in:
- Journal of Practical Electrocardiology, 2018, v. 27, n. 3, p. 169, doi. 10.13308/j.issn.2095-9354.2018.03.002
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- Publication type:
- Article
Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias.
- Published in:
- Frontiers in Physiology, 2012, v. 3, p. 1, doi. 10.3389/fphys.2012.00346
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- Publication type:
- Article
How do hypertrophic cardiomyopathy mutationsaffect myocardial function in carriers with normalwall thickness? Assessment with cardiovascularmagnetic resonance.
- Published in:
- Journal of Cardiovascular Magnetic Resonance (BioMed Central), 2010, v. 12, p. 13, doi. 10.1186/1532-429X-12-13
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- Publication type:
- Article
Long-term reliability of the phospholamban (PLN) p.(Arg14del) risk model in predicting major ventricular arrhythmia: a landmark study.
- Published in:
- EP: Europace, 2024, v. 26, n. 4, p. 1, doi. 10.1093/europace/euae069
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- Publication type:
- Article
Insights into adherence to medication and lifestyle recommendations in an international cohort of patients with catecholaminergic polymorphic ventricular tachycardia.
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- EP: Europace, 2024, v. 26, n. 2, p. 1, doi. 10.1093/europace/euae044
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- Article
The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview.
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- EP: Europace, 2023, v. 25, n. 11, p. 1, doi. 10.1093/europace/euad336
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- Publication type:
- Article
Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome.
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- EP: Europace, 2023, v. 25, n. 11, p. 1, doi. 10.1093/europace/euad319
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- Publication type:
- Article
Manual vs. automatic assessment of the QT-interval and corrected QT.
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- EP: Europace, 2023, v. 25, n. 9, p. 1, doi. 10.1093/europace/euad213
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- Publication type:
- Article
Arrhythmogenic vulnerability of re-entrant pathways in post-infarct ventricular tachycardia assessed by advanced computational modelling.
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- EP: Europace, 2023, v. 25, n. 9, p. 1, doi. 10.1093/europace/euad198
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- Publication type:
- Article
Risk stratification of sudden cardiac death: a review.
- Published in:
- EP: Europace, 2023, v. 25, n. 8, p. 1, doi. 10.1093/europace/euad203
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- Publication type:
- Article
Successful defibrillation testing in patients undergoing elective subcutaneous implantable cardioverter-defibrillator generator replacement.
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- EP: Europace, 2023, v. 25, n. 7, p. 1, doi. 10.1093/europace/euad184
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- Article
RYR2-ryanodinopathies: from calcium overload to calcium deficiency.
- Published in:
- EP: Europace, 2023, v. 25, n. 6, p. 1, doi. 10.1093/europace/euad156
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- Publication type:
- Article
Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2.
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- EP: Europace, 2023, v. 25, n. 5, p. 1, doi. 10.1093/europace/euad094
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- Publication type:
- Article
Non-invasive stereotactic arrhythmia radiotherapy for ventricular tachycardia: results of the prospective STARNL-1 trial.
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- EP: Europace, 2023, v. 25, n. 3, p. 1015, doi. 10.1093/europace/euad020
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- Publication type:
- Article
Reduction in long-term mortality using remote device monitoring in a large real-world population of patients with implantable defibrillators.
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- EP: Europace, 2023, v. 25, n. 3, p. 969, doi. 10.1093/europace/euac280
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- Publication type:
- Article
Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia.
- Published in:
- 2023
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- Publication type:
- journal article
Effectiveness and safety of mexiletine in patients at risk for (recurrent) ventricular arrhythmias: a systematic review.
- Published in:
- 2022
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- Publication type:
- journal 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
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey.
- Published in:
- 2022
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- Publication type:
- journal article
Comparing clinical performance of current implantable cardioverter-defibrillator implantation recommendations in arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- 2022
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- Publication type:
- journal article
Life-threatening arrhythmias with autosomal recessive TECRL variants.
- Published in:
- 2021
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- journal article
Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing.
- Published in:
- 2021
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- Publication type:
- journal article
Complications related to elective generator replacement of the subcutaneous implantable defibrillator.
- Published in:
- 2021
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- Publication type:
- journal article
Using registries to predict outcome: the implantable cardioverter-defibrillator in long QT syndrome.
- Published in:
- 2019
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- Publication type:
- journal article
Support vector machine-based assessment of the T-wave morphology improves long QT syndrome diagnosis.
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- 2018
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- Publication type:
- journal article
Device orientation of a leadless pacemaker and subcutaneous implantable cardioverter-defibrillator in canine and human subjects and the effect on intrabody communication.
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- 2018
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- Publication type:
- journal article
Therapeutic approaches for Long QT syndrome type 3: an update.
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- 2018
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- Publication type:
- editorial
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.
- Published in:
- 2017
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- Publication type:
- journal article
Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy.
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- 2016
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- Publication type:
- journal article
Improving usual care after sudden death in the young with focus on inherited cardiac diseases (the CAREFUL study): a community-based intervention study.
- Published in:
- 2016
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- Publication type:
- journal article
Inherited ion channel diseases: a brief review.
- Published in:
- 2015
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- Publication type:
- journal article
Early mortality in prophylactic implantable cardioverter-defibrillator recipients: development and validation of a clinical risk score.
- Published in:
- 2014
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- Publication type:
- Journal Article
Andersen-Tawil syndrome, scarier for the doctor than for the patient? Who, when, and how to treat.
- Published in:
- 2013
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- Publication type:
- Journal Article
Andersen–Tawil syndrome, scarier for the doctor than for the patient? Who, when, and how to treat.
- Published in:
- EP: Europace, 2013, v. 15, n. 12, p. 1690, doi. 10.1093/europace/eut326
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- Publication type:
- Article
Ventricular dysfunction in a family with long QT syndrome type 3.
- Published in:
- 2013
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- Publication type:
- Journal Article
Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome.
- Published in:
- EP: Europace, 2011, v. 13, n. 7, p. 968, doi. 10.1093/europace/eur011
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- Publication type:
- Article
TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.
- Published in:
- Journal of Cardiovascular Development & Disease (JCDD), 2023, v. 10, n. 11, p. 455, doi. 10.3390/jcdd10110455
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- Publication type:
- Article
Clinical utility gene card for: Long-QT Syndrome (types 1-13).
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1, doi. 10.1038/ejhg.2013.28
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- Article
Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 4031, doi. 10.3390/ijms24044031
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- Publication type:
- Article
Left Axis Deviation in Brugada Syndrome: Vectorcardiographic Evaluation during Ajmaline Provocation Testing Reveals Additional Depolarization Abnormalities.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 2, p. 484, doi. 10.3390/ijms22020484
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- Publication type:
- Article
Multimodal explainable artificial intelligence identifies patients with non-ischaemic cardiomyopathy at risk of lethal ventricular arrhythmias.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-65357-x
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- Article
Optimal echocardiographic assessment of myocardial dysfunction for arrhythmic risk stratification in phospholamban mutation carriers.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2022, v. 23, n. 11, p. 1492, doi. 10.1093/ehjci/jeab178
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- Publication type:
- Article
Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imaging.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2019, v. 20, n. 1, p. 92, doi. 10.1093/ehjci/jey047
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- Publication type:
- Article
Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14).
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 1, doi. 10.1038/ejhg.2010.243
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- Publication type:
- Article
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 7, p. 820, doi. 10.1038/ejhg.2011.33
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- Publication type:
- Article