(Q73885519)

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Long QT syndrome

scientific article published on 01 May 2000

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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Europe PubMed Central

Long QT syndrome (English)

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

G M Vincent

1

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7 November 2019

publication date

1 May 2000

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Cardiology clinics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

18

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Europe PubMed Central

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7 November 2019

2

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

309-325

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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

1 reference

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7 January 2021

based on heuristic

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Mechanisms in adrenergic dependent onset of torsades de pointes

1 reference

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7 January 2021

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Clinical relevance of cardiac arrhythmias generated by afterdepolarizations. Role of M cells in the generation of U waves, triggered activity and torsade de pointes.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of M cells in acquired long QT syndrome, U waves, and torsade de pointes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Optical Mapping of Drug-Induced Polymorphic Arrhythmias and Torsade de Pointes in the Isolated Rabbit Heart

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Efficacy of left cardiac sympathectomy in the treatment of patients with the long QT syndrome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Nicorandil suppresses a hump on the monophasic action potential and torsade de pointes in a patient with idiopathic long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The long QT syndrome and torsade de pointes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism of arrhythmogenicity of the short-long cardiac sequence that precedes ventricular tachyarrhythmias in the long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Electrophysiological mechanism of the characteristic electrocardiographic morphology of torsade de pointes tachyarrhythmias in the long-QT syndrome: detailed analysis of ventricular tridimensional activation patterns

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Diabetic autonomic neuropathy and the heart.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Time- and rate-dependent alterations of the QT interval precede the onset of torsade de pointes in patients with acquired QT prolongation.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Long QT Genotype Can Be Identified by ECG Phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Early afterdepolarizations: mechanism of induction and block. A role for L-type Ca2+ current

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The surdo-cardiac syndrome: three new cases of congenital deafness with syncopal attacks and Q-T prolongation in the electrocardiogram

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Rate-dependent prolongation of cardiac action potentials by a methanesulfonanilide class III antiarrhythmic agent. Specific block of rapidly activating delayed rectifier K+ current by dofetilide

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

QT interval prolongation and sudden cardiac death in diabetic autonomic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal response to exercise, face immersion, and isoproterenol in children with the long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The long QT syndrome: a prospective international study

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Electrocardiographic and electrophysiologic studies in patients with torsades de pointe--role of monophasic action potentials

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Low penetrance in the long-QT syndrome: clinical impact

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management part III

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Electrophysiological mechanisms in a canine model of erythromycin-associated long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes. Mechanism of action

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac sympathetic innervation and the sudden infant death syndrome. A possible pathogenetic link

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Pathogenesis and therapy of the idiopathic long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Cellular basis for the ECG features of the LQT1 form of the long-QT syndrome: effects of beta-adrenergic agonists and antagonists and sodium channel blockers on transmural dispersion of repolarization and torsade de pointes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsade des pointes in LQT2 and LQT3 models of the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The inward rectification mechanism of the HERG cardiac potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular basis of the long-QT syndrome associated with deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Rate adaptation of QT intervals during and after exercise in children with congenital long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning of a membrane protein that induces a slow voltage-gated potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term (subacute) potassium treatment in congenital HERG-related long QT syndrome (LQTS2)

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Electrophysiologic mechanisms of the long QT interval syndromes and torsade de pointes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Heterogeneity in the inherited long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Mode of onset of torsade de pointes in congenital long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevention of torsade de pointes in the congenital long QT syndrome: use of a pause prevention pacing algorithm.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation of a heart potassium channel by protein kinase A and C

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The congenital long QT syndromes in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional distribution of right and left stellate innervation to the ventricles. Production of neurogenic electrocardiographic changes by unilateral alteration of sympathetic tone

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Potassium channels: basic aspects, functional roles, and medical significance

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of Early Afterdepolarization in Familial Long QTU Syndrome and Torsade de Pointes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Sudden Cardiac Death

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8651%2805%2970143-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0733-8651(05)70143-0

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10849875%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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