(Q36791113)

16 August 2017

1 reference

title

Risk factors in sudden death in epilepsy (SUDEP): the quest for mechanisms (English)

1 reference

16 August 2017

Lina Nashef

1

1 reference

16 August 2017

Neeti Hindocha

series ordinal

2

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16 August 2017

Andrew Makoff

series ordinal

3

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16 August 2017

language of work or name

1 reference

13 April 2007

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16 August 2017

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16 August 2017

volume

48

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16 August 2017

issue

5

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16 August 2017

page(s)

859-871

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

16 August 2017

cites work

1 reference

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21 January 2018

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Single nucleotide polymorphism map of five long-QT genes.

21 January 2018

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First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

21 January 2018

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

21 January 2018

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Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

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Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy

21 January 2018

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A potassium channel mutation in neonatal human epilepsy

21 January 2018

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Oxygen desaturations triggered by partial seizures: implications for cardiopulmonary instability in epilepsy

21 January 2018

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Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

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Calcium-dependent inactivation of neuronal calcium channels

21 January 2018

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Ca2+-induced Ca2+ release supports the relay mode of activity in thalamocortical cells.

21 January 2018

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Sudden unexpected death in people with epilepsy: a pediatric perspective

21 January 2018

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

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Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels

21 January 2018

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

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SNP S1103Y in the cardiac sodium channel gene SCN5A is associated with cardiac arrhythmias and sudden death in a white family

21 January 2018

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KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

21 January 2018

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Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

21 January 2018

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Cloning and characterization of alpha1H from human heart, a member of the T-type Ca2+ channel gene family

21 January 2018

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KCNE2 modulates current amplitudes and activation kinetics of HCN4: influence of KCNE family members on HCN4 currents.

21 January 2018

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The cardiac sodium channel mRNA is expressed in the developing and adult rat and human brain.

21 January 2018

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Prospective cohort study of prone sleeping position and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Mortality of epilepsy in developed countries: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Identification and differential subcellular localization of the neuronal class C and class D L-type calcium channel alpha 1 subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sudden withdrawal of carbamazepine increases cardiac sympathetic activity in sleep

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sodium-channel defects in benign familial neonatal-infantile seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Central apnea and acute cardiac ischemia in a sheep model of epileptic sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Ryanodine receptor-mediated intracellular calcium release in rat cerebellar Purkinje neurones

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sudden unexpected death in epilepsy: a series of witnessed deaths.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Case-control study of SUDEP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Cardiac ryanodine receptor function and regulation in heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Cause-specific mortality in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

L-type calcium channels: the low down

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Molecular basis of an inherited epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Distinct subcellular localization of different sodium channel alpha and beta subunits in single ventricular myocytes from mouse heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Functional role of L-type Cav1.3 Ca2+ channels in cardiac pacemaker activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Partial cloning and differential expression of ryanodine receptor/calcium-release channel genes in human tissues including the hippocampus and cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

The MinK-related peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Ankyrin-based cardiac arrhythmias: a new class of channelopathies due to loss of cellular targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A cardiac arrhythmia syndrome caused by loss of ankyrin-B function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Differential distribution of four hyperpolarization-activated cation channels in mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Antiepileptic drug therapy and its management in sudden unexpected death in epilepsy: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Risk factors for sudden unexpected death in epilepsy: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Does cardiac conduction pathology contribute to sudden unexpected death in epilepsy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Heart rate and EKG changes in 102 seizures: analysis of influencing factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Isolation and characterization of cDNAs encoding human brain ankyrins reveal a family of alternatively spliced genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Novel vistas of calcium-mediated signalling in the thalamus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Carbamazepine affects autonomic cardiac control in patients with newly diagnosed epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Preoperative heart rate variability in relation to surgery outcome in refractory epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.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.1528-1167.2007.01082.X

Genetics of cardiac arrhythmias and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

MiRP1 modulates HCN2 channel expression and gating in cardiac myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Molecular cloning and expression of a human heart inward rectifier potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

KCNQ potassium channels: physiology, pathophysiology, and pharmacology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: implications for therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Cardiac arrhythmias in focal epilepsy: a prospective long-term study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Pacemaker channel dysfunction in a patient with sinus node disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Stillbirths, sudden infant deaths, and long-QT syndrome: puzzle or mosaic, the pieces of the Jigsaw are being fitted together

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Molecular characterization of a slowly gating human hyperpolarization-activated channel predominantly expressed in thalamus, heart, and testis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Long-term prognosis of seizures with onset in childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Postictal central apnea as a cause of SUDEP: evidence from near-SUDEP incident.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.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.1528-1167.2007.01082.X

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Mutations in EFHC1 cause juvenile myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sudden unexplained death in epilepsy (SUDEP) following previous seizure-related pulmonary oedema: case report and review of possible preventative treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Electrocardiograph QT lengthening associated with epileptiform EEG discharges--a role in sudden unexplained death in epilepsy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sudden unexpected death in epilepsy: is carbamazepine implicated?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

M-type KCNQ2-KCNQ3 potassium channels are modulated by the KCNE2 subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Heart rate variability in patients with epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.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.1528-1167.2007.01082.X

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Functional characterization and neuronal modeling of the effects of childhood absence epilepsy variants of CACNA1H, a T-type calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.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.1528-1167.2007.01082.X

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Sudden unexplained death in children with epilepsy: a cohort study with an eighteen-year follow-up.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Variability of antiepileptic medication taking behaviour in sudden unexplained death in epilepsy: hair analysis at autopsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Localization of Nav1.5 sodium channel protein in the mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Tissue and species distribution of mRNA for the IKr-like K+ channel, erg.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

Molecular diagnosis in a child with sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2007.01082.X

10.1111/J.1528-1167.2007.01082.X

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference