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Publications by Louise Harris

Striking in Vivo Phenotype of a Disease-Associated Human SCN5A Mutation Producing Minimal Changes in Vitro

Cardiovascular Medicine

English

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Genetic Variants in SCN5A Promoter Are Associated With Arrhythmia Phenotype Severity in Patients With Heterozygous Loss-Of-Function Mutation

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SCN5A Mutation Associated With Acute Myocardial Infarction

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Genotype-Phenotype Relationship and Risk Stratification in Loss-Of-Function SCN5A Mutation Carriers

Annals of Noninvasive Electrocardiology

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Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease

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R222Q Nav1.5 Mutation Associated With a New SCN5A-Related Cardiac Arrhythmia

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A Novel SCN5A Mutation Associated With Drug Induced Brugada Type ECG

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Changes in Phenotype and Differentiation Potential of Human Mesenchymal Stem Cells Aging in Vitro

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In Vitro and in Vivo Changes in Human Complement Caused by Silage

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Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient With Overlap Syndrome Due to the E1784K SCN5A Mutation

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Internal Medicine

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