Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families. - Wikidata - awgldk - TriplyDB

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

http://www.wikidata.org/entity/Q33156318

about

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death Channelopathies Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions The molecular autopsy: should the evaluation continue after the funeral?Molecular autopsy in victims of inherited arrhythmias 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the Ion channel macromolecular complexes in cardiomyocytes: roles in sudden cardiac death Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy Part 10: Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Evaluating the role of Cardiac Genetics Nurses in inherited cardiac conditions services using a Maturity Matrix.Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study.Comparative study of CMR characteristics between arrhythmogenic right ventricular cardiomyopathy patients with/without syncope.Symptoms Before Sudden Arrhythmic Death Syndrome: A Nationwide Study Among the Young in Denmark.Inpatient detection of cardiac-inherited disease: the impact of improving family history taking Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.Long QT molecular autopsy in sudden infant death syndrome.Sudden cardiac death in the young (5-39 years) in the canton of Vaud, Switzerland.Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.Family-based associations in measures of psychological distress and quality of life in a cardiac screening clinic for inheritable cardiac diseases: a cross-sectional study Inherited cardiac arrhythmias: diagnosis, treatment, and prevention.Soccer and Sudden Cardiac Death in Young Competitive Athletes: A Review.Sudden Unexplained Death - Treating the Family.Genetic screening in sudden cardiac death in the young can save future lives Assessing the knowledge of sudden unexpected death in the young among Canadian medical students and recent graduates: a cross-sectional study Sudden unexplained cardiac arrest in apparently healthy children: a single-center experience The spectrum of epidemiology underlying sudden cardiac death.The investigation of sudden arrhythmic death syndrome (SADS)-the current approach to family screening and the future role of genomics and stem cell technology.Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations.Sudden Cardiac Death in the Young Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention The molecular autopsy: an indispensable step following sudden cardiac death in the young?Presymptomatic diagnosis of Fabry's disease: a case report.Cardiac gene defects can cause sudden cardiac death in young people.Sudden death in persons younger than 40 years of age: incidence and causes.The magnitude of sudden cardiac death in the young: a death certificate-based review in England and Wales.Cardiac channelopathies and sudden infant death syndrome.Reprogramming cellular identity for regenerative medicine.

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P2860

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

http://www.wikidata.org/entity/Q33156318

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European Heart Journal

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Chrysoula Dalageorgou

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Edward Rowland

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Michael Christiansen

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Petros Syrris

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Sian Hughes

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Steve Jeffery

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William J McKenna

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P2860

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

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10.1093/EURHEARTJ/EHN219

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Maria Teresa Tome Esteban

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5341761

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