Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
about
Functional effects of KCNE3 mutation and its role in the development of Brugada syndromeTransmural expression of transient outward potassium current subunits in normal and failing canine and human heartsSex differences in the mechanisms underlying long QT syndromeIonic mechanisms of arrhythmogenesisTransient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndromeAllitridi inhibits multiple cardiac potassium channels expressed in HEK 293 cellsProperties and molecular determinants of the natural flavone acacetin for blocking hKv4.3 channelsBrugada syndrome in the paediatric population: a comprehensive approach to clinical manifestations, diagnosis, and management.Drug-induced Brugada syndrome.Mode of onset of ventricular fibrillation in patients with early repolarization pattern vs. Brugada syndromePrognosis after implantation of cardioverter-defibrillators in Korean patients with Brugada syndrome.Risk stratification and treatment of brugada syndrome.[Ion channel diseases in children].[Brugada ECG].Clinical characterisation and long-term prognosis of women with Brugada syndrome.Molecular determinants of cardiac transient outward potassium current (I(to)) expression and regulationAbnormal repolarization as the basis for late potentials and fractionated electrograms recorded from epicardium in experimental models of Brugada syndrome.J wave syndromes.Genetics of sudden cardiac death.Distinctive electrophysiological characteristics of right ventricular out-flow tract cardiomyocytes.The electrocardiographic abnormalities in highly trained athletes compared to the genetic study related to causes of unexpected sudden cardiac death.Brugada syndrome and ischemia-induced ST-segment elevation. Similarities and differences.Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome.Brugada syndrome: from cell to bedsideRationale for the use of the terms J-wave syndromes and early repolarization.The J Wave Syndromes and their Role in Sudden Cardiac Death.Brugada phenocopy: A new electrocardiogram phenomenonMolecular genetics of arrhythmias and cardiovascular conditions associated with arrhythmias.Inherited arrhythmic disorders: long QT and Brugada syndromesMolecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis.Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome.ECG repolarization waves: their genesis and clinical implications.Unraveling the Enigma of Bangungut: Is Sudden Unexplained Nocturnal Death Syndrome (SUNDS) in the Philippines a Disease Allelic to the Brugada Syndrome?In silico Prediction of Sex-Based Differences in Human Susceptibility to Cardiac Ventricular TachyarrhythmiasMechanisms of disease: current understanding and future challenges in Brugada syndrome.Electrophysiological basis and genetics of Brugada syndrome.Basis for the Induction of Tissue-Level Phase-2 Reentry as a Repolarization Disorder in the Brugada SyndromeIonic and cellular mechanisms underlying the development of acquired Brugada syndrome in patients treated with antidepressants.Lack of Influence of the Androgen Receptor Gene CAG-Repeat Polymorphism on Clinical and Electrocardiographic Manifestations of the Brugada Syndrome in Man.
P2860
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P2860
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@en
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@nl
type
label
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@en
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@nl
prefLabel
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@en
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@nl
P2093
P50
P1433
P1476
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
@en
P2093
Andrew C Zygmunt
Jeffrey M Fish
Jonathan M Cordeiro
José M Di Diego
Robert J Goodrow
P304
P356
10.1161/01.CIR.0000032002.22105.7A
P407
P577
2002-10-01T00:00:00Z