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1. Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. Issue 7 (5th July 2016)

2. Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. Issue 7 (July 2016)

3. Identifying sex-based differences in heart failure with preserved ejection fraction. (31st December 2022)

4. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Issue 4 (28th July 2020)