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You searched for: Author/Creator Wilde, Arthur A.M.

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52. SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families. (December 2020)

53. SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers. (1st September 2018)

54. Sex- and age specific association of new-onset atrial fibrillation with in-hospital mortality in hospitalised COVID-19 patients. (April 2022)

55. ST-Segment Elevation and Fractionated Electrograms in Brugada Syndrome Patients Arise From the Same Structurally Abnormal Subepicardial RVOT Area but Have a Different Mechanism. (December 2015)

56. Sudden Cardiac Arrest and Rare Genetic Variants in the Community. (April 2016)

57. Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration. (January 2021)

58. The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity. Issue 5 (18th August 2017)

60. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy. (3rd November 2016)