Arthur A. M. Wilde

发表

Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications.

A. Zwinderman, Y. Pinto, A. Wilde, 2013, International journal of cardiology.

Ventricular fibrillation in MYH7-related hypertrophic cardiomyopathy before onset of ventricular hypertrophy.

I. V. van Langen, I. Christiaans, Ronald H. Lekanne dit Deprez, 2009, Heart rhythm.

Multifocal Ectopic Purkinje-related Premature Contractions a New Scn5a-related Cardiac Channelopathy

F. Charpentier, Y. Coudière, C. Thauvin-Robinet, 2022 .

Genetic basis of hypertrophic cardiomyopathy

S. Ommen, T. Spelsberg, I. Christiaans, 2010 .

Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood.

M. P. van den Berg, C. Bezzina, A. Wilde, 2005, Journal of the American College of Cardiology.

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy

I. van der Made, E. Creemers, P. Postema, 2018, European heart journal.

clinical aspects of type 3 long-Qt syndrome an international Multicenter study

Derick R. Peterson, E. Kaufman, J. Towbin, 2016 .

clinical aspects of type 3 long-Qt syndrome an international Multicenter study

Derick R. Peterson, E. Kaufman, J. Towbin, 2016 .

clinical aspects of type 3 long-Qt syndrome an international Multicenter study

Derick R. Peterson, E. Kaufman, J. Towbin, 2016 .

clinical aspects of type 3 long-Qt syndrome an international Multicenter study

Derick R. Peterson, E. Kaufman, J. Towbin, 2016 .

clinical aspects of type 3 long-Qt syndrome an international Multicenter study

Derick R. Peterson, E. Kaufman, J. Towbin, 2016 .

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

F. Fellmann, A. Sajantila, Arthur A. M. Wilde, 2023 .

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

I. V. Van Gelder, A. Wilde, M. Rook, 1999, Cardiovascular research.

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Voltage – Dependent L-Type Calcium Channel

R. Brugada, A. Wilde, Arthur A. M. Wilde, 2011 .

Ventricular tachycardia in the infarcted, Langendorff-perfused human heart: role of the arrangement of surviving cardiac fibers.

A. Wilde, T. Opthof, R. Coronel, 1990, Journal of the American College of Cardiology.

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Kevin Knight, D. O’Regan, Y. Pinto, 2023, medRxiv.

Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death Single-Center

Yolan J. Reckman, P. Postema, N. Lahrouchi, 2017 .

Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases

A. Wilde, M. P. van den Berg, M. Ackerman, 2018, Circulation. Genomic and precision medicine.

Loss-of-function Sodium Channel Mutations in Infancy a Pattern Unfolds Article See P 14

P. Chockalingam, Arthur A. M. Wilde, 2022 .

Combined effects of hypoxia, hyperkalemia and acidosis on membrane action potential and excitability of guinea-pig ventricular muscle.

D Durrer, M J Janse, A. Wilde, 1984, Journal of molecular and cellular cardiology.

The brisk-standing-test for long QT syndrome in prepubertal school children: defining normal.

T. Delhaas, A. Wilde, P. Postema, 2018, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

ECG determinants in adult patients with chronic right ventricular pressure overload caused by congenital heart disease: relation with plasma neurohormones and MRI parameters

A. Wilde, E. E. van der Wall, B. Mulder, 2002, Heart.

Homozygous premature truncation of the HERG protein : the human HERG knockout.

A. Wilde, T. Hoorntje, N. Sreeram, 1999, Circulation.

Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period

E. Hoogerwaard, E. Bakker, Arthur A. M. Wilde, 1997, Journal of Neurology.