(Q36362468)

13 August 2017

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title

Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation (English)

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13 August 2017

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4

Günter Breithardt

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13 August 2017

Horst Wedekind

1

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13 August 2017

Eric Schulze-Bahr

2

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13 August 2017

Volker Debus

3

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13 August 2017

Bernd Brinkmann

5

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13 August 2017

Thomas Bajanowski

6

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13 August 2017

publication date

6 January 2006

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International Journal of Legal Medicine

13 August 2017

published in

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13 August 2017

volume

121

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13 August 2017

issue

4

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13 August 2017

page(s)

245-257

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The long QT syndrome in children. An international study of 287 patients

13 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

21 January 2018

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Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

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%2FS00414-005-0069-3

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%2FS00414-005-0069-3

Survivors of Out-of-Hospital Cardiac Arrest With Apparently Normal Heart: Need for Definition and Standardized Clinical Evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

Epidemiology of idiopathic cardiomyopathies in children and adolescents. A nationwide study in Finland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

Epidemiology of Hypertrophic Cardiomyopathy–Related Death

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00414-005-0069-3

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

21 January 2018

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12 December 2020

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

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12 December 2020

Apical hypertrophic cardiomyopathy: the continuing saga

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12 December 2020

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

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12 December 2020

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

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12 December 2020

Congenital heart disease and sudden death in the young

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12 December 2020

Familial dilated cardiomyopathy: from clinical presentation to molecular genetics.

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12 December 2020

Sudden death in children and adolescents

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12 December 2020

Sudden cardiac death in childhood.

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12 December 2020

Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene

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12 December 2020

Thrombosis and acute coronary-artery lesions in sudden cardiac ischemic death

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12 December 2020

The congenital long QT syndromes in childhood

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12 December 2020

The long QT syndromes: genetic basis and clinical implications

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12 December 2020

Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases

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12 December 2020

Sudden infant death syndrome: how significant are the cardiac channelopathies?

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12 December 2020

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

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12 December 2020

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

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12 December 2020

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

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12 December 2020

Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunitalphai2.

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12 December 2020

Sudden unexpected death in children and adolescents

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12 December 2020

Idiopathic ventricular fibrillation

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12 December 2020

Identification of infants destined to die unexpectedly during infancy: evaluation of predictive importance of prolonged apnoea and disorders of cardiac rhythm or conduction

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12 December 2020

The Brugada syndrome: clinical, electrophysiologic and genetic aspects.

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12 December 2020

Familial occurrence of right ventricular dysplasia: a study involving nine families

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12 December 2020

Arrhythmogenic right ventricular dysplasia: a United States experience

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12 December 2020

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

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12 December 2020

Brugada syndrome and sudden cardiac death in children

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12 December 2020

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

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12 December 2020

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

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12 December 2020

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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12 December 2020

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Short QT Syndrome: a familial cause of sudden death

1 reference

12 December 2020

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

1 reference

12 December 2020

De novo mutation in the SCN5A gene associated with early onset of sudden infant death

1 reference

12 December 2020

Dilated cardiomyopathy caused by plasma membrane carnitine transport defect

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12 December 2020

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

12 December 2020

Prevalence and clinical course of the juveniles with Brugada-type ECG in Japanese population

1 reference

12 December 2020

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

1 reference

12 December 2020

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

1 reference

12 December 2020

Prolongation of the QT interval and the sudden infant death syndrome.

1 reference

12 December 2020

Risk stratification in the long-QT syndrome.

1 reference

12 December 2020

Supraventricular tachycardia in children: Clinical features, response to treatment, and long-term follow-up in 217 patients

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12 December 2020

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

1 reference

12 December 2020

Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response

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12 December 2020

Radiofrequency ablation in children with asymptomatic Wolff-Parkinson-White syndrome

1 reference

12 December 2020

Novel Brugada SCN5A mutation causing sudden death in children

1 reference

12 December 2020

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

1 reference

12 December 2020

Sudden cardiac death in young people with apparently normal heart

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12 December 2020

Catecholinergic ventricular tachycardia in children

1 reference

12 December 2020

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

1 reference

12 December 2020

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

1 reference

12 December 2020

A molecular link between the sudden infant death syndrome and the long-QT syndrome

1 reference

12 December 2020

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

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12 December 2020

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

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12 December 2020

Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children

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12 December 2020

Right ventricular cardiomyopathy and sudden death in young people

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12 December 2020

10.1007/S00414-005-0069-3

Identifiers

DOI

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13 August 2017

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