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1. A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family. Issue 12 (26th June 2018)

2. Device interaction between cardiac contractility modulation (CCM) and subcutaneous defibrillator (S‐ICD). (22nd September 2021)

4. High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature. Issue 1 (January 2015)

5. High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature. Issue 1 (January 2015)

6. Propofol dose and efficacy of defibrillation testing during implantation of subcutaneous implantable cardioverter‐defibrillators: A retrospective, single center cohort study. (9th December 2022)

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

9. Transgenic short-QT syndrome 1 rabbits mimic the human disease phenotype with QT/action potential duration shortening in the atria and ventricles and increased ventricular tachycardia/ventricular fibrillation inducibility. (28th November 2018)

10. Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing. Issue 5 (16th December 2020)