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Brugada syndromeThe Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceJ-wave syndromes: Brugada and early repolarization syndromesBrugada Syndrome:Risk Stratification And ManagementTransient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndromeBrugada syndrome in the paediatric population: a comprehensive approach to clinical manifestations, diagnosis, and management.Effect of Wenxin Keli and quinidine to suppress arrhythmogenesis in an experimental model of Brugada syndrome.Variable electrocardiographic effects of short-term quinidine sulfate administration in Brugada syndrome.Arrhythmic storm responsive to quinidine in a patient with Brugada syndrome and vasovagal syncope.Monomorphic ventricular tachycardia due to Brugada syndrome successfully treated by hydroquinidine therapy in a 3-year-old child.Risk stratification and treatment of brugada syndrome.Risk Stratification and Therapeutic Approach in Brugada Syndrome.Brugada syndrome in the young: an assessment of risk factors predicting future events.Brugada Syndrome:Risk Stratification And Management.Empiric quinidine therapy for asymptomatic Brugada syndrome: time for a prospective registry.J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledgeSpecific therapy based on the genotype and cellular mechanism in inherited cardiac arrhythmias. Long QT syndrome and Brugada syndromeMechanisms of disease: current understanding and future challenges in Brugada syndrome.Electrophysiological basis and genetics of Brugada syndrome.Therapy for the Brugada syndrome.Brugada Syndrome: Clinical, Genetic, Molecular, Cellular, and Ionic Aspects.Electrical storms in Brugada syndrome: review of pharmacologic and ablative therapeutic options.Ionic basis of pharmacological therapy in Brugada syndrome.The genetic component of Brugada syndromeRole of late sodium current in modulating the proarrhythmic and antiarrhythmic effects of quinidineNovel Therapeutic Strategies for the Management of Ventricular Arrhythmias Associated with the Brugada SyndromeBrugada Syndrome and Early Repolarisation: Distinct Clinical Entities or Different Phenotypes of the Same Genetic Disease?Genetics of sudden death: focus on inherited channelopathies.Brugada syndrome: an update.Genetic biomarkers in Brugada syndrome.Brugada syndrome: a heterogeneous disease with a common ECG phenotype?Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy.Pharmacotherapy for inherited arrhythmia syndromes: mechanistic basis, clinical trial evidence and practical application.Advances in the pharmacologic treatment of ventricular arrhythmias.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Brugada syndrome in children - Stepping into unchartered territory.Drug Therapy For Preventing Ventricular Arrhythmia In Brugada syndrome: Do We Have The Answers Yet?Genetic testing in specific cardiomyopathies.In vivo human demonstration of phase 2 reentry.Brugada syndrome: Controversies in Risk stratification and Management.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Hydroquinidine therapy in Brugada syndrome.
@ast
Hydroquinidine therapy in Brugada syndrome.
@en
type
label
Hydroquinidine therapy in Brugada syndrome.
@ast
Hydroquinidine therapy in Brugada syndrome.
@en
prefLabel
Hydroquinidine therapy in Brugada syndrome.
@ast
Hydroquinidine therapy in Brugada syndrome.
@en
P2093
P1476
Hydroquinidine therapy in Brugada syndrome.
@en
P2093
Antoine Leenhardt
Bruno Cauchemez
Geneviève Jarry
Isabelle Denjoy
Jean-Luc Rey
Jean-Sylvain Hermida
Jérôme Clerc
Paul Milliez
Stefania Di Fusco
P304
P356
10.1016/J.JACC.2003.12.046
P407
P577
2004-05-01T00:00:00Z