about
Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmiasGenetics of inherited primary arrhythmia disordersLong-QT syndrome: from genetics to managementMolecular pathogenesis of long QT syndrome type 1Molecular pathogenesis of long QT syndrome type 2Right ventricular monophasic action potentials in patients with long QT syndromeResponse of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndromeRegulation of KCNQ/Kv7 family voltage-gated K+ channels by lipids.Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeationKCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.Left stellate ganglionectomy for the long Q-T interval syndrome: nine-year follow-up of a patient.Mouse models of long QT syndrome.Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.Left ventricular mechanical dispersion by tissue Doppler imaging: a novel approach for identifying high-risk individuals with long QT syndrome.Identification of a possible pathogenic link between congenital long QT syndrome and epilepsyQTc: how long is too long?The prevalence and diagnostic/prognostic utility of sinus arrhythmia in the evaluation of congenital long QT syndromePharmacological and non-pharmacological management of the congenital long QT syndrome: the rationaleLong QT syndrome: a Korean single center study.Importance of QT interval in clinical practice.Evaluation and Management of Athletes With Long QT Syndrome.Cardiac arrhythmias misdiagnosed as epilepsyHereditary prolongation of QT interval . Study of two families.Hereditary prolongation of QT intervalSurdo-cardiac syndrome: incidence among children in schools for the deaf.Asystole 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.Prenylamine-induced ventricular tachycardia and syncope controlled by ventricular pacingInvasive electrophysiological study in the Jervell and Lange-Nielsen syndromeEpiglottitis and torsade de pointes tachycardiaAnalysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.Locus heterogeneity of autosomal dominant long QT syndrome.Molecular genetic aspects of the Romano-Ward long QT syndrome.Cardiac arrest: a rare complication of pallid syncope?Consanguinity, cardiac arrest, hearing impairment, and ECG abnormalities: counselling pitfalls in the Romano-Ward syndrome.Familial ventricular tachycardia: a report of four families.Dynamics of ventricular repolarisation in the congenital long QT syndromes.Study of left and right ventricular function in Romano-Ward syndrome.
P2860
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P2860
description
1964 nî lūn-bûn
@nan
1964 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1964 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1964年の論文
@ja
1964年論文
@yue
1964年論文
@zh-hant
1964年論文
@zh-hk
1964年論文
@zh-mo
1964年論文
@zh-tw
1964年论文
@wuu
name
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.
@ast
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.
@en
type
label
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.
@ast
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.
@en
prefLabel
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.
@ast
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.
@en
P1476
A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN
@en
P2093
P304
P577
1964-04-01T00:00:00Z