(Q37793374)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Johan Duflou

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Christopher Semsarian

series ordinal

4

object named as

Christopher Semsarian

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

author name string

Emily Tu

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

publication date

28 September 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

page(s)

201-208

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20875080%20AND%20SRC:MED&resulttype=core&format=json

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

14 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

Sudden unexplained death and injury in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

Cardiorespiratory findings in sudden unexplained/unexpected death in epilepsy (SUDEP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

New SCN5A mutation in a SUDEP victim with idiopathic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

Cardiac sodium channel gene variants and sudden cardiac death in women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

Cardiac sodium channel dysfunction in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

Lengthening of corrected QT during epileptic seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2010.00438.X