Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.
about
KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channelProperties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmiasCellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndromeVentricular repolarization measures for arrhythmic risk stratificationThe history, hotspots, and trends of electrocardiogramGenetics of inherited primary arrhythmia disordersNeuronal and Cardiovascular Potassium Channels as Therapeutic Drug Targets: Promise and PitfallsLong-QT syndrome: from genetics to managementMolecular pathogenesis of long QT syndrome type 1Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriersRight 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 syndromeElectrophysiological mechanisms of long and short QT syndromes.Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations.Regulation of KCNQ/Kv7 family voltage-gated K+ channels by lipids.New criteria of indication and selection of patients to cochlear implant.Inherited diseases of the inner ear in man in the light of studies on the mousePROFOUND CHILDHOOD DEAFNESS.Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.Left cardiac sympathetic denervation in long QT syndrome patients.Andersen syndrome autosomal dominant in three generations.QTc dispersion measurement for risk of syncope in patients with aortic stenosis.Familial qt prolongation and risk of sudden death.Perioperative management of long QT syndrome in a child with congenital heart disease.The clinical significance of QTc dispersion measurement for risk of syncope in patients with aortic stenosis.Long QT syndrome: first and fatal events provoked by hemodialysis.KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.Role of early afterdepolarization in familial long QTU syndrome and torsade de pointes.GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).Novel compound heterozygous mutations in the KCNQ1 gene associated with autosomal recessive long QT syndrome (Jervell and Lange-Nielsen syndrome).PITUITARY TUMOR, QT PROLONGATION AND VENTRICULAR ARRHYTHMIA.Left stellate ganglionectomy for the long Q-T interval syndrome: nine-year follow-up of a patient.Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.Mouse models of long QT syndrome.Congenital myocardial sympathetic dysinnervation (CMSD)--a structural defect of idiopathic long QT syndrome.Identification 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 epilepsyChannelopathies: Brugada syndrome, long QT syndrome, short QT syndrome, and CPVT.
P2860
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P2860
Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.
description
1957 nî lūn-bûn
@nan
1957 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1957 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1957年の論文
@ja
1957年論文
@yue
1957年論文
@zh-hant
1957年論文
@zh-hk
1957年論文
@zh-mo
1957年論文
@zh-tw
1957年论文
@wuu
name
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@ast
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@en
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@nl
type
label
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@ast
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@en
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@nl
prefLabel
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@ast
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@en
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@nl
P1476
Congenital deaf-mutism, functi ...... Q-T interval and sudden death.
@en
P2093
LANGE-NIELSEN F
P356
10.1016/0002-8703(57)90079-0
P407
P577
1957-07-01T00:00:00Z