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「"Behr ER "[Author]」の検索結果

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

Noncardiac genetic predisposition in sudden infant death syndrome.

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.

Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case Series.

Gender Differences in Patients with Brugada Syndrome and Arrhythmic Events: Data from a Survey on Arrhythmic Events in 678 Patients.

Diagnostic Yield of Genetic Testing in Young Athletes with T-wave Inversion.

Sudden Cardiac Death: Pharmacotherapy and Proarrhythmic Drugs: A Nationwide Cohort Study in Denmark.

Lack of genotype-phenotype correlation in families who had Brugada syndrome and sudden arrhythmic death syndrome with reported pathogenic SCN1B variants.

Fever-Related Arrhythmic Events in the Multicenter Survey on Arrhythmic Events in Brugada Syndrome (SABRUS).

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

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

Proof of concept study of a novel pacemapping algorithm as a basis to guide ablation of ventricular arrhythmias.

Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes.

Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

Obesity and sudden cardiac death in the young: Clinical and pathological insights from a large national registry.

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients.

Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort.

Sudden infant death syndrome and inherited cardiac conditions.

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