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Genetic testing for inherited arrhythmia syndromes and cardiomyopathies: results of the European Heart Rhythm Association survey.
- Published in:
- EP: Europace, 2024, v. 26, n. 9, p. 1, doi. 10.1093/europace/euae216
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- Article
Autopsy of all young sudden death cases is important to increase survival in family members left behind.
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- EP: Europace, 2024, v. 26, n. 6, p. 1, doi. 10.1093/europace/euae128
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- Publication type:
- Article
The role for ambulatory electrocardiogram monitoring in the diagnosis and prognostication of Brugada syndrome: a sub-study of the Rare Arrhythmia Syndrome Evaluation (RASE) Brugada study.
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- EP: Europace, 2024, v. 26, n. 5, p. 1, doi. 10.1093/europace/euae091
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- 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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- Publication type:
- Article
Yield of molecular autopsy in sudden cardiac death in athletes: data from a large registry in the UK.
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- EP: Europace, 2024, v. 26, n. 2, p. 1, doi. 10.1093/europace/euae029
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- Article
Is right ventricular outflow tract epicardial substrate ablation the standard of care in high-risk Brugada syndrome?
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- EP: Europace, 2024, v. 26, n. 1, p. 1, doi. 10.1093/europace/euae020
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- Article
From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies.
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- EP: Europace, 2023, v. 25, n. 8, p. 1, doi. 10.1093/europace/euad180
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- Article
Should lethal arrhythmias in hypertrophic cardiomyopathy be predicted using non-electrophysiological methods?
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- EP: Europace, 2023, v. 25, n. 5, p. 1, doi. 10.1093/europace/euad045
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- Article
Implantable loop recorders in Brugada syndrome.
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- EP: Europace, 2023, v. 25, n. 2, p. 775, doi. 10.1093/europace/euac149
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- Publication type:
- Article
European Society of Cardiology quality indicators for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed in collaboration with the European Heart Rhythm Association of the European Society of Cardiology
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- EP: Europace, 2023, v. 25, n. 1, p. 199, doi. 10.1093/europace/euac114
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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
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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- journal article
Brugada syndrome and arrhythmogenic cardiomyopathy: overlapping disorders of the connexome?
- Published in:
- 2021
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- Publication type:
- journal article
Diagnosis, family screening, and treatment of inherited arrhythmogenic diseases in Europe: results of the European Heart Rhythm Association Survey.
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- 2020
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- Publication type:
- journal article
Diagnostic yield of hypertrophic cardiomyopathy in first-degree relatives of decedents with idiopathic left ventricular hypertrophy.
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- 2020
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- Publication type:
- journal article
Electrocardiographic differentiation between 'benign T-wave inversion' and arrhythmogenic right ventricular cardiomyopathy.
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- 2019
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- Publication type:
- journal article
Proof of concept study of a novel pacemapping algorithm as a basis to guide ablation of ventricular arrhythmias.
- Published in:
- 2018
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- Publication type:
- journal article
Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- 2016
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- Publication type:
- journal article
Author's reply: To PMID 24585884.
- Published in:
- 2015
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- Publication type:
- commentary
Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions.
- Published in:
- EP: Europace, 2014, v. 16, n. 12, p. 1706, doi. 10.1093/europace/euu037
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- Publication type:
- Article
The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths.
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- EP: Europace, 2014, v. 16, n. 6, p. 899, doi. 10.1093/europace/eut329
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- Publication type:
- Article
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
- Published in:
- 2013
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- Publication type:
- Journal Article
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
- Published in:
- EP: Europace, 2013, v. 15, n. 10, p. 1389
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- Publication type:
- Article
Familial cardiological evaluation in sudden arrhythmic death syndrome: essential but challenging.
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- EP: Europace, 2013, v. 15, n. 7, p. 924, doi. 10.1093/europace/eut060
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- Publication type:
- Article
Acquired long QT syndrome: as risky as congenital long QT syndrome?
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- EP: Europace, 2012, v. 14, n. 3, p. 310, doi. 10.1093/europace/eur372
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- Publication type:
- Article
Benign or malignant, early or delayed: the changing face of early repolarization.
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- EP: Europace, 2012, v. 14, n. 1, p. 5, doi. 10.1093/europace/eur326
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- Publication type:
- Article
Prevalence of the type 1 Brugada electrocardiogram in Caucasian patients with suspected coronary spasm.
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- EP: Europace, 2011, v. 13, n. 11, p. 1625, doi. 10.1093/europace/eur205
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- Publication type:
- Article
Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity.
- Published in:
- 2022
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- Publication type:
- journal article
Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, p. 17, doi. 10.1111/epi.13232
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- Publication type:
- Article
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy.
- Published in:
- 2019
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- Publication type:
- journal article
337: MUTATIONS IN CALMODULIN AND VENTRICULAR TACHYCARDIA, SYNCOPE AND SUDDEN CARDIAC DEATH.
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- Cardiovascular Journal of Africa, 2013, v. 24, n. 1, p. 280
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- Publication type:
- Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1409, doi. 10.1038/ng1113-1409b
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- Publication type:
- Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
- Published in:
- Nature Genetics, 2013, v. 45, n. 9, p. 1044, doi. 10.1038/ng.2712
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- Publication type:
- Article
Hourly variability in outflow tract ectopy as a predictor of its site of origin.
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- Journal of Cardiovascular Electrophysiology, 2022, v. 33, n. 1, p. 7, doi. 10.1111/jce.15295
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- Article
Cheek smear analysis as a prognostic tool in children with arrhythmogenic cardiomyopathy.
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- Cardiology in the Young, 2022, v. 32, p. S51
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- Publication type:
- Article
Cheek smear analysis as a prognostic tool in children with arrhythmogenic cardiomyopathy.
- Published in:
- Cardiology in the Young, 2022, v. 32, n. S2, p. S51, doi. 10.1017/S1047951122001950
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- Publication type:
- Article
Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0078511
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- Article
Brugada syndrome: can polygenic risk scores help the clinician?
- Published in:
- European Heart Journal, 2024, v. 45, n. 26, p. 2333, doi. 10.1093/eurheartj/ehae364
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- Publication type:
- Article
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.
- Published in:
- European Heart Journal, 2023, v. 44, n. 35, p. 3357, doi. 10.1093/eurheartj/ehad418
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- Article
Device-related complications in subcutaneous versus transvenous ICD: a secondary analysis of the PRAETORIAN trial.
- Published in:
- European Heart Journal, 2022, v. 43, n. 47, p. 4872, doi. 10.1093/eurheartj/ehac496
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- Publication type:
- Article
2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed by the task force for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death of the European Society of Cardiology (ESC) Endorsed by the Association for European Paediatric and Congenital Cardiology (AEPC)
- Published in:
- European Heart Journal, 2022, v. 43, n. 40, p. 3997, doi. 10.1093/eurheartj/ehac262
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- Publication type:
- Article
Explaining the unexplained: applying genetic testing after cardiac arrest and sudden death.
- Published in:
- European Heart Journal, 2022, v. 43, n. 32, p. 3082, doi. 10.1093/eurheartj/ehac172
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- Publication type:
- Article
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics.
- Published in:
- European Heart Journal, 2022, v. 43, n. 20, p. 1901, doi. 10.1093/eurheartj/ehab895
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- Publication type:
- Article
European Cardiac Arrhythmia Genetics (ECGen) Focus Group.
- Published in:
- European Heart Journal, 2022, v. 43, n. 20, p. 1891, doi. 10.1093/eurheartj/ehab698
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- Article
Application of artificial intelligence to the electrocardiogram.
- Published in:
- European Heart Journal, 2021, v. 42, n. 46, p. 4717, doi. 10.1093/eurheartj/ehab649
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- Publication type:
- Article
Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway?
- Published in:
- European Heart Journal, 2021, v. 42, n. 11, p. 1073, doi. 10.1093/eurheartj/ehaa1051
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- Publication type:
- Article
Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine.
- Published in:
- European Heart Journal, 2020, v. 41, n. 5, p. 614, doi. 10.1093/eurheartj/ehaa041
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- Publication type:
- Article
Genetic susceptibility and the Brugada syndrome.
- Published in:
- European Heart Journal, 2019, v. 40, n. 37, p. 3094, doi. 10.1093/eurheartj/ehz448
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- Publication type:
- Article
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.
- Published in:
- European Heart Journal, 2019, v. 40, n. 35, p. 2964, doi. 10.1093/eurheartj/ehz311
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- Publication type:
- Article
A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2013, v. 24, n. 5, p. 562, doi. 10.1111/jce.12068
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- Publication type:
- Article