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■ Search Result - Abbreviation : LQT1

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Abbreviation: LQT1
Appearance Frequency: 112 time(s)
Long forms: 29

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
long QT syndrome type 1
(63 times)
Cardiology
(26 times)
LQT2 (6 times)
LQTS (6 times)
EADs (4 times)
2000 Long QT syndrome: ionic basis and arrhythmia mechanism in long QT syndrome type 1.
LQTS type 1
(17 times)
Cardiology
(12 times)
LQTS (16 times)
LQT2 (5 times)
LQT3 (2 times)
2004 Temporal repolarization lability differences among genotyped patients with the long QT syndrome.
long-QT type 1
(4 times)
Cardiology
(2 times)
LMC (2 times)
APD (1 time)
DA (1 time)
2008 Phenotypic variability in Caucasian and Japanese patients with matched LQT1 mutations.
long QT1
(3 times)
Cardiology
(2 times)
APD (2 times)
AP (1 time)
APD90 (1 time)
2004 Electrophysiologic effects of nicorandil on the guinea pig long QT1 syndrome model.
25-lead electrocardiograms in nine asymptomatic KCNQ1 mutation carriers
(1 time)
Cardiology
(1 time)
--- 2008 Electrocardiographic interventricular dispersion of repolarization during autonomic adaptation in LQT1 subtype of long QT syndrome.
located on chromosome 7 and KVLQT1
(1 time)
Medicine
(1 time)
--- 1996 The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biology.
location of mutations across KCNQ1
(1 time)
Cardiology
(1 time)
LQTS (1 time)
2009 Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
long QT syndrome due to KCNQ1
(1 time)
Cardiology
(1 time)
--- 2001 [T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].
long QT syndrome genes, namely, KCNQ1
(1 time)
Genetics, Medical
(1 time)
SNPs (1 time)
2004 Single nucleotide polymorphism map of five long-QT genes.
10  long QT syndrome genotypes in KCNQ1
(1 time)
Gynecology
(1 time)
--- 2019 Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study.
11  long-QT1 syndrome
(1 time)
Cardiology
(1 time)
--- 2002 Differentiation between LQT1 and LQT2 patients and unaffected subjects using 24-hour electrocardiographic recordings.
12  LQT genes have been identified: KVLQT1
(1 time)
Medicine
(1 time)
LQT (1 time)
QTc (1 time)
1998 Genetics, molecular mechanisms and management of long QT syndrome.
13  LQT has been identified on chromosome 11p15.5
(1 time)
Biology
(1 time)
LQT (1 time)
1995 Readjusting the localization of long QT syndrome gene on chromosome 11p15.
14  LQT loci on chromosomes 11
(1 time)
Cell Biology
(1 time)
LQT (1 time)
1995 A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.
15  LQT syndrome type 1
(1 time)
Science
(1 time)
ECG (1 time)
hERG (1 time)
Ks (1 time)
2012 Modulation of hERG potassium channel gating normalizes action potential duration prolonged by dysfunctional KCNQ1 potassium channel.
16  LQT1 but not in control patients during epinephrine
(1 time)
Cardiology
(1 time)
LQTS (1 time)
SD-DeltaRR (1 time)
2005 Response of beat-by-beat QT variability to sympathetic stimulation in the LQT1 form of congenital long QT syndrome.
17  LQT3 are caused by mutations in KCNQ1
(1 time)
Cardiology
(1 time)
LQTS (1 time)
2015 Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction.
18  LQTS associated with missense variants in KCNQ1
(1 time)
Chemistry
(1 time)
ECG (1 time)
LQTS (1 time)
2022 Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes.
19  LQTS caused by the KCNQ1 potassium channel gene mutations
(1 time)
Cardiology
(1 time)
HR (1 time)
LQTS (1 time)
2003 Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
20  LQTS due to mutation of the KCNQ1 gene
(1 time)
Genetics, Medical
(1 time)
BWS (1 time)
LQTS (1 time)
SRS (1 time)
2013 Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p.
21  LQTS genes; KCNQ1/KVLQT1
(1 time)
Cardiology
(1 time)
HR (1 time)
LQTS (1 time)
microV-TWA (1 time)
2003 Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndrome.
22  LQTS genotypes included type 1
(1 time)
Cardiology
(1 time)
AED (1 time)
ICD (1 time)
LCSD (1 time)
2015 Automated external defibrillator rescues among children with diagnosed and treated long QT syndrome.
23  LQTS have been mapped to chromosome 11p15.5
(1 time)
Cardiology
(1 time)
LQTS (1 time)
SSCP (1 time)
1998 New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
24  LQTS-associated genes KCNQ1
(1 time)
Natural Science Disciplines
(1 time)
LQTS (1 time)
MP (1 time)
NPSs (1 time)
2018 Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use.
25  LQTS-causing channel genes, KCNQ1
(1 time)
Cardiology
(1 time)
CPVT (1 time)
2004 Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.
26  LQTS-causing mutations in KCNQ1
(1 time)
Cardiology
(1 time)
LQTS (1 time)
2005 Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
27  LQTS-causing potassium channel genes: KCNQ1
(1 time)
Medicine
(1 time)
LQTS (1 time)
2003 Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.
28  LQTS-susceptibility genes: KCNQ1
(1 time)
Cardiology
(1 time)
LQTS (1 time)
2009 Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
29  LQTS: KCNQ1
(1 time)
Cardiology
(1 time)
LQT4 (1 time)
2005 Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects.