Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
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Andersen‐Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneityCongenital long QT syndromes: clinical features, molecular genetics and genetic testing.Ventricular ectopy during REM sleep: implications for nocturnal sudden cardiac death.Electrocardiogram in Andersen-Tawil syndrome. New electrocardiographic criteria for diagnosis of type-1 Andersen-Tawil syndrome.Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7).Primary periodic paralyses.Inherited arrhythmic disorders in Japan.Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent.Genetic defects in the hotspot of inwardly rectifying K(+) (Kir) channels and their metabolic consequences: a reviewKCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.Thyrotoxic Periodic Paralysis: Case Reports and an Up-to-Date Review of the Literature.The primary periodic paralyses: diagnosis, pathogenesis and treatment.Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndromeGene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies.In vivo and in vitro functional characterization of Andersen's syndrome mutations.Flecainide ameliorates arrhythmogenicity through NCX flux in Andersen-Tawil syndrome-iPS cell-derived cardiomyocytes.Phosphatidylinositol-4,5-bisphosphate is required for KCNQ1/KCNE1 channel function but not anterograde trafficking.Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.Electrophysiological mechanisms of ventricular arrhythmias in relation to Andersen-Tawil syndrome under conditions of reduced IK1: a simulation study.Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.Lack of Any Cardiac Involvement in a Patient with Andersen-Tawil Syndrome Associated with the c.574A→G Mutation in KCNJ2
P2860
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P2860
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@ast
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@en
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@nl
type
label
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@ast
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@en
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@nl
prefLabel
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@ast
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@en
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@nl
P2093
P1433
P1476
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
@en
P2093
Hideo Otani
Keiko Tsuji
Minoru Horie
Shozo Nakano
Tomohiko Ai
Yoshihiro Kubo
Yuichiro Fujiwara
P304
P356
10.1161/01.CIR.0000019906.35135.A3
P407
P577
2002-06-04T00:00:00Z