Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases. (Q37793374)

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14 February 2020

title

Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases (English)

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14 February 2020

1 reference

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14 February 2020

1 reference

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14 February 2020

Christopher Semsarian

series ordinal

object named as

Christopher Semsarian

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14 February 2020

Emily Tu

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14 February 2020

publication date

28 September 2010

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14 February 2020

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14 February 2020

volume

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14 February 2020

issue

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14 February 2020

page(s)

201-208

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Sudden death in epilepsy: a study of incidence in a young cohort with epilepsy and learning difficulty.

14 February 2020

cites work

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Sudden unexplained death and injury in epilepsy

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Incidence and risk factors in sudden unexpected death in epilepsy: a prospective cohort study

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Sudden unexpected death in epilepsy: a review of incidence and risk factors

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Sudden unexpected death in epilepsy (SUDEP): update and reflections.

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

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

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SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome

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

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

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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

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Mutations in the hminK gene cause long QT syndrome and suppress lKs function

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

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

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

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Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

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Mutations in alpha-actinin-2 cause hypertrophic cardiomyopathy: a genome-wide analysis

21 January 2018

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Post-mortem pathologic and genetic studies in "dead in bed syndrome" cases in type 1 diabetes mellitus

21 January 2018

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New SCN5A mutation in a SUDEP victim with idiopathic epilepsy

21 January 2018

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

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Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes

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Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

21 January 2018

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Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.

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

21 January 2018

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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

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Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants

21 January 2018

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Cardiac sodium channel gene variants and sudden cardiac death in women

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Cardiac sodium channel dysfunction in sudden infant death syndrome.

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

21 January 2018

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Pathologic cardiac repolarization in pharmacoresistant epilepsy and its potential role in sudden unexpected death in epilepsy: A case-control study

21 January 2018

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