Letter: Digoxin immunoassay with use of [3H]digoxin vs. [125I]tyrosine-methyl-ester of digoxin

Familial Mahaim syndrome.

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Baroreflex sensitivity and heart rate variability in the identification of patients at risk for life-threatening arrhythmias: implications for clinical trials.

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Electrocardiographic features of inherited diseases that predispose to the development of cardiac arrhythmias, long QT syndrome, arrhythmogenic right ventricular cardiomyopathy/dysplasia, and Brugada syndrome.

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Journal of cardiovascular electrophysiology·2000

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: need for an international registry. Study Group on Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy of the Working Groups on Myocardial and Pericardial Disease and Arrhythmias of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the World Heart Federation.

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Reproducible Amyloid Typing by Data-Independent Acquisition Mass Spectrometry.

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Canadian journal of physiology and pharmacology·2026

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ACS omega·2026

Beyond GCP: developing a differentiated competency framework for principal investigators in innovative drug clinical trials in China.

Frontiers in medicine·2026

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ACS omega·2026

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International journal of pharmaceutics·2026

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Letter: Digoxin immunoassay with use of [3H]digoxin vs. [125I]tyrosine-methyl-ester of digoxin

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