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「"Bastiaenen R "[Author]」の検索結果

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Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentation.

The narrow-sense and common single nucleotide polymorphism heritability of early repolarization.

Electrocardiographic differentiation between 'benign T-wave inversion' and arrhythmogenic right ventricular cardiomyopathy.

Pulmonary embolism and infarction with a paradoxical thrombus visualised in both atria.

A Fibrillating Left Atrial Appendage During Sinus Rhythm.

The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy.

Apical ballooning (takotsubo) syndrome with concurrent ST-segment elevation myocardial infarction.

Reply: Are T-Inversions in Chest Leads Always Benign?

Anterior T-Wave Inversion in Young White Athletes and Nonathletes: Prevalence and Significance.

Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

The Ventricular Ectopic QRS Interval (VEQSI): Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy in Patients with Incomplete Disease Expression.

Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy.

Echocardiographic Assessment of Mantle Radiation Mitral Stenosis.

Feasibility and Efficacy of Simultaneous Pulmonary Vein Isolation and Cavotricuspid Isthmus Ablation using Cryotherapy.

Prevalence of electrocardiographic anomalies in young individuals: relevance to a nationwide cardiac screening program.

Clinical Usefulness, Angiographic Characteristics and Safety Evaluation of Intracoronary Acetylcholine Provocation Testing Among 921 Consecutive Caucasian Patients with Unobstructed Coronary Arteries.

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes.

Clinical significance of electrocardiographic right ventricular hypertrophy in athletes: comparison with arrhythmogenic right ventricular cardiomyopathy and pulmonary hypertension.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

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