26 results on '"van Tintelen, J. Peter"'
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2. Integrating Exercise Into Personalized Ventricular Arrhythmia Risk Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy
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
6. Abstract 19832: De Novo Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Are Rare and Associated With Large Deletions
7. Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients
8. Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis
9. Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers
10. Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy
11. Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy
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
15. Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy
16. Pregnancy, cardiomyopathies, and genetics
17. Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 yearsʼ experience
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
21. Counsel the genotype, treat the phenotype
22. Familial dilated cardiomyopathy: another risk factor for anthracycline-induced cardiotoxicity?
23. Lamin A/C-related cardiac disease and pregnancy
24. The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening
25. DNA Analysis in Inherited Cardiomyopathies: Current Status and Clinical Relevance
26. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics
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