about
QT interval and dispersion in primary autonomic failureLong-QT syndrome: from genetics to managementAn LQTS6 MiRP1 mutation suppresses pacemaker current and is associated with sinus bradycardiaAdrenergaically mediated ventricular fibrillation in probucol-treated dogs: roles of alpha and beta adrenergic receptorsRight ventricular monophasic action potentials in patients with long QT syndromeArrhythmogenic potential of diuretic induced hypokalaemia in patients with mild hypertension and ischaemic heart diseaseResponse of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndromeTorsades de pointes, a common arrhythmia, induced by medicationGene-specific paradoxical QT responses during rapid eye movement sleep in women with congenital long QT syndromeCardiac pacing in the long QT syndrome: review of available data and practical recommendations.Sleep-disordered breathing: effects on brain structure and function.Left cardiac sympathetic denervation in long QT syndrome patients.Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis.Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.Perioperative management of long QT syndrome in a child with congenital heart disease.QTc prolongation in apheresis platelet donors.KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.Left stellate ganglionectomy for the long Q-T interval syndrome: nine-year follow-up of a patient.Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.Congenital myocardial sympathetic dysinnervation (CMSD)--a structural defect of idiopathic long QT syndrome.Value of history-taking in syncope patients: in whom to suspect long QT syndrome?Depressive symptoms in the congenital long QT syndrome.Pharmacological and non-pharmacological management of the congenital long QT syndrome: the rationaleCongenital and drug-induced long-QT syndrome: an update.Video-Assisted Thoracoscopic Left Cardiac Sympathetic Denervation in Patients with Hereditary Ventricular Arrhythmias.Cardiac arrhythmias misdiagnosed as epilepsyAsystole in the prolonged QT syndromeA case of the cardio-auditory syndrome (long QT interval and profound deafness) diagnosed in the perinatal period and kept under surveillance for two years.Early afterdepolarization abolished by potassium channel opener in a patient with idiopathic long QT syndrome.Heterogeneity in the inherited long QT syndrome.Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.Molecular genetic aspects of the Romano-Ward long QT syndrome.Prenatal findings in patients with prolonged QT interval in the neonatal period.Neurological aspects of sinoatrial heart block.Recent trends in the management of life-threatening ventricular arrhythmiasStudy of left and right ventricular function in Romano-Ward syndrome.QT prolongation is associated with increased mortality in end stage liver disease.Cerebral blood flow velocity and vasomotor reactivity during autonomic challenges in heart failure.Evidence of a long QT founder gene with varying phenotypic expression in South African families.Abnormal myelin and axonal integrity in recently diagnosed patients with obstructive sleep apnea.
P2860
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P2860
description
1975 nî lūn-bûn
@nan
1975 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1975 թվականի մարտին հրատարակված գիտական հոդված
@hy
1975年の論文
@ja
1975年論文
@yue
1975年論文
@zh-hant
1975年論文
@zh-hk
1975年論文
@zh-mo
1975年論文
@zh-tw
1975年论文
@wuu
name
The long Q-T syndrome.
@ast
The long Q-T syndrome.
@en
type
label
The long Q-T syndrome.
@ast
The long Q-T syndrome.
@en
prefLabel
The long Q-T syndrome.
@ast
The long Q-T syndrome.
@en
P2093
P1476
The long Q-T syndrome.
@en
P2093
P304
P356
10.1016/0002-8703(75)90089-7
P407
P577
1975-03-01T00:00:00Z