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1. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study

2. Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies

3. Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family members

4. Sex-specific aspects of phospholamban cardiomyopathy: The importance and prognostic value of low-voltage electrocardiograms

6. Electrocardiographic Findings in Patients with Arrhythmogenic Cardiomyopathy and Right Bundle Branch Block Ventricular Tachycardia

7. The genetic architecture of Plakophilin 2 cardiomyopathy

8. Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy

9. Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmogenic right ventricular cardiomyopathy type 5

10. 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

12. Distinct molecular signature of phospholamban p.Arg14del arrhythmogenic cardiomyopathy

13. Flotillins in the intercalated disc are potential modulators of cardiac excitability

16. Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel

17. Phospholamban immunostaining is a highly sensitive and specific method for diagnosing phospholamban p.Arg14del cardiomyopathy

18. Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentation

19. Isolated Subepicardial Right Ventricular Outflow Tract Scar in Athletes With Ventricular Tachycardia

20. QRS prolongation after premature stimulation is associated with polymorphic ventricular tachycardia in nonischemic cardiomyopathy: Results from the Leiden Nonischemic Cardiomyopathy Study

21. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

22. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population

24. Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy

26. Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome

27. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy According to Revised 2010 Task Force Criteria With Inclusion of Non-Desmosomal Phospholamban Mutation Carriers

28. Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications

29. Left-dominant arrhythmogenic cardiomyopathy in a large family: Associated desmosomal or nondesmosomal genotype?

30. Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

31. Mortality Risk of Untreated Myosin-Binding Protein C–Related Hypertrophic Cardiomyopathy

32. Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

33. Genotype-Phenotype Analysis in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Follow-Up of a Large Series of Dutch Index-Patients and Family Members

34. Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

36. The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

37. Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene

40. Familial disease with a risk of sudden death: A longitudinal study of the psychological consequences of predictive testing for long QT syndrome

41. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

42. Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene

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