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The long QT syndromes: genetic basis and clinical implications
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
The long QT syndromes: genetic basis and clinical implications
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
author name string
C E Chiang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
D M Roden
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
language of work or name
English
0 references
publication date
1 July 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
published in
Journal of the American College of Cardiology
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
volume
36
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
page(s)
1-12
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
cites work
Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death
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Functional distribution of right and left stellate innervation to the ventricles. Production of neurogenic electrocardiographic changes by unilateral alteration of sympathetic tone
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Electrical alternation of the T-wave: Clinical and experimental evidence of its relationship with the sympathetic nervous system and with the long Q-T syndrome
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The long Q-T syndrome
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Idiopathic long QT syndrome: progress and questions
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Crossref
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7 January 2021
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The long QT syndrome: a prospective international study
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Crossref
reference URL
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7 January 2021
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Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
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Crossref
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7 January 2021
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Locus heterogeneity of autosomal dominant long QT syndrome
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the hminK gene cause long QT syndrome and suppress IKs function
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of the long-QT syndrome associated with deafness.
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
KCNE1 mutations cause jervell and Lange-Nielsen syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
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Crossref
reference URL
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Low penetrance in the long-QT syndrome: clinical impact
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
The long QT syndrome: ion channel diseases of the heart
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of genetic heterogeneity in the long QT syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A recessive variant of the Romano-Ward long-QT syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family of potassium channel genes related to eag in Drosophila and mammals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutation in the pore region of HERG causes familial long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human delta1261 mutation of the HERG potassium channel results in a truncated protein that contains a subunit interaction domain and decreases the channel expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous premature truncation of the HERG protein : the human HERG knockout.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A minK-HERG complex regulates the cardiac potassium current I(Kr)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Drug-induced torsades de pointes in one patient with congenital long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. Online
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular mechanism for an inherited cardiac arrhythmia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A single Na(+) channel mutation causing both long-QT and Brugada syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Subunit composition of minK potassium channels.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Involvement of IsK-associated K+ channel in heart rate control of repolarization in a murine engineered model of Jervell and Lange-Nielsen syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new form of long QT syndrome associated with syndactyly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT syndrome associated with syndactyly identified in females
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome. LQTS Investigators
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
QT dispersion: an indication of arrhythmia risk in patients with long QT intervals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cellular basis for the normal T wave and the electrocardiographic manifestations of the long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Quantitative analysis of T wave abnormalities and their prognostic implications in the idiopathic long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The long QT syndrome with impaired atrioventricular conduction: a malignant variant in infants.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The electrophysiological mechanism of ventricular arrhythmias in the long QT syndrome. Tridimensional mapping of activation and recovery patterns
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic criteria for the long QT syndrome. An update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Combined use of beta-adrenergic blocking agents and long-term cardiac pacing for patients with the long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dispersion of the QT interval. A marker of therapeutic efficacy in the idiopathic long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of congenital long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The automatic implantable cardioverter-defibrillator in young patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early afterdepolarization abolished by potassium channel opener in a patient with idiopathic long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900716-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0735-1097(00)00716-6
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
PubMed ID
10898405
1 reference
stated in
Europe PubMed Central
PubMed ID
10898405
retrieved
30 July 2017
ResearchGate publication ID
12421638
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