(Q38118161)

29 August 2017

title

Genetic etiology and evaluation of sudden cardiac death (English)

1 reference

29 August 2017

3

Patrick T Ellinor

1 reference

29 August 2017

4

Steven A Lubitz

1 reference

29 August 2017

2

Saagar Mahida

1 reference

29 August 2017

1

Elena Dolmatova

1 reference

29 August 2017

publication date

1 August 2013

1 reference

Current cardiology reports

29 August 2017

published in

1 reference

29 August 2017

volume

15

1 reference

29 August 2017

issue

8

1 reference

29 August 2017

page(s)

389

1 reference

Heart Disease and Stroke Statistics--2013 Update: A Report From the American Heart Association

29 August 2017

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Long-term follow-up of patients with short QT syndrome

21 January 2018

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Short QT syndrome: from bench to bedside.

21 January 2018

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Short QT syndrome: pharmacological treatment

21 January 2018

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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

21 January 2018

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The prevalence of Brugada ECG in adult patients in a large university hospital in the western United States

21 January 2018

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Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study

21 January 2018

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Prevalence and mortality of the Brugada-type electrocardiogram in one city in Japan.

21 January 2018

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21 January 2018

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Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry

21 January 2018

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Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry.

21 January 2018

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Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

21 January 2018

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Natural history of Brugada syndrome: insights for risk stratification and management

21 January 2018

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Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

21 January 2018

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The early repolarization normal variant electrocardiogram: correlates and consequences

21 January 2018

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Familial sudden cardiac death associated with a terminal QRS abnormality on surface 12-lead electrocardiogram in the index case

21 January 2018

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Ventricular fibrillation in a patient with prominent J (Osborn) waves and ST segment elevation in the inferior electrocardiographic leads: a Brugada syndrome variant?

21 January 2018

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Clinical characteristics of patients with spontaneous or inducible ventricular fibrillation without apparent heart disease presenting with J wave and ST segment elevation in inferior leads

21 January 2018

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Characterization of J wave in a patient with idiopathic ventricular fibrillation.

21 January 2018

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The early repolarization pattern in the general population: clinical correlates and heritability

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

21 January 2018

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21 January 2018

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

21 January 2018

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Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

21 January 2018

1 reference

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Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical practice. Hypertrophic obstructive cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Hypertrophic cardiomyopathy in 2012

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical profile and significance of delayed enhancement in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Myocardial Scar Visualized by Cardiovascular Magnetic Resonance Imaging Predicts Major Adverse Events in Patients With Hypertrophic Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Prognostic significance of myocardial fibrosis in hypertrophic cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Idiopathic cardiomyopathy in the United States, 1970-1982.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Truncations of titin causing dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

The mutations associated with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Right ventricular dysplasia: a report of 24 adult cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Right ventricular cardiomyopathy and sudden death in young people

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Natural history and risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Arrhythmogenic right ventricular dysplasia: a United States experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Sudden death in the young: what do we know about it and how to prevent?

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Expression and function of dipeptidyl-aminopeptidase-like protein 6 as a putative beta-subunit of human cardiac transient outward current encoded by Kv4.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Recurrent cardiac events in patients with idiopathic ventricular fibrillation, excluding patients with the Brugada syndrome

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Malignant entity of idiopathic ventricular fibrillation and polymorphic ventricular tachycardia initiated by premature extrasystoles originating from the right ventricular outflow tract

21 January 2018

1 reference

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Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Genetic variation in SCN10A influences cardiac conduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic

21 January 2018

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Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease

21 January 2018

1 reference

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Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Genetics and cardiovascular disease: a policy statement from the American Heart Association.

21 January 2018

1 reference

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Age- and Training-Dependent Development of Arrhythmogenic Right Ventricular Cardiomyopathy in Heterozygous Plakoglobin-Deficient Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0389-8

Heritability of early repolarization: a population-based study

21 January 2018

1 reference

12 December 2020

Incidence and predictors of implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary prevention

1 reference

12 December 2020

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

1 reference

12 December 2020

Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome

1 reference

12 December 2020

Prevention of sudden cardiac death

1 reference

12 December 2020

2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

1 reference

12 December 2020

Low penetrance in the long-QT syndrome: clinical impact

1 reference

12 December 2020

Determinants of Sudden Cardiac Death in Individuals With the Electrocardiographic Pattern of Brugada Syndrome and No Previous Cardiac Arrest

1 reference

12 December 2020

Familial polymorphic ventricular arrhythmias: a quarter century of successful medical treatment based on serial exercise-pharmacologic testing

1 reference

12 December 2020

Long-term follow-up of idiopathic ventricular fibrillation ablation: a multicenter study

1 reference

12 December 2020

RS-T segment elevation in mid- and left precordial leads as a normal variant

1 reference

12 December 2020

A previously undescribed congenital malformation of the heart: almost total absence of the myocardium of the right ventricle

1 reference

12 December 2020

Genetic screening and risk assessment in hypertrophic cardiomyopathy

1 reference

12 December 2020

Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands

1 reference

12 December 2020

Relation between severity of left-ventricular hypertrophy and prognosis in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Gating Properties of SCN5A Mutations and the Response to Mexiletine in Long-QT Syndrome Type 3 Patients

1 reference

12 December 2020

Prevalence of the brugada syndrome in an apparently healthy population

1 reference

12 December 2020

Systematic Assessment of Patients With Unexplained Cardiac Arrest

1 reference

12 December 2020

Effect of clinical phenotype on yield of long QT syndrome genetic testing

1 reference

12 December 2020

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

1 reference

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Cardiac arrest during long-distance running races

1 reference

12 December 2020

Molecular genetics of cardiomyopathy: changing times, shifting paradigms

1 reference

12 December 2020

10.1007/S11886-013-0389-8

Identifiers

DOI

1 reference

Dimensions Publication ID

29 August 2017

1005360088

0 references

1 reference