Cardiac channel molecular autopsy for sudden unexpected death in epilepsy (Q38417008)

2 September 2017

title

Cardiac channel molecular autopsy for sudden unexpected death in epilepsy (English)

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2 September 2017

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Michael J Ackerman

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2 September 2017

Jonathan N Johnson

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2 September 2017

David J Tester

series ordinal

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2 September 2017

Nancy E Bass

series ordinal

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2 September 2017

publication date

15 April 2010

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Journal of Child Neurology

2 September 2017

published in

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2 September 2017

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2 September 2017

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2 September 2017

page(s)

916-921

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

2 September 2017

cites work

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https://api.crossref.org/works/10.1177%2F0883073809343722

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

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/10.1177%2F0883073809343722

A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Sudden cardiac death with apparently normal heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Sudden death in patients without structural heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Cardiac channelopathies: it's in the genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Postmortem molecular screening in unexplained sudden death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Postmortem long QT syndrome genetic testing for sudden unexplained death in the young

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

New SCN5A mutation in a SUDEP victim with idiopathic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Report of the American Epilepsy Society and the Epilepsy Foundation joint task force on sudden unexplained death in epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809343722

21 January 2018

Identifiers

DOI

10.1177/0883073809343722

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2 September 2017

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