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Your search keyword '"van Tintelen, J. Peter"' showing total 26 results

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26 results on '"van Tintelen, J. Peter"'

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3. Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration

4. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

5. Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome

7. Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients

9. Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers

12. The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics

13. The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus

14. Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers

18. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers

19. Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy

20. Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

24. The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

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