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2. Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia*

10. Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features

11. Recurrent and founder mutations in the Netherlands – Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy*

12. Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia*

21. The Netherlands Arrhythmogenic Cardiomyopathy Registry: design and status update.

22. Conductive reserve and arrhythmias

26. The Brugada Numbers (reply to letter)

29. Poster Session 4

30. Poster Session 2

31. Poster Session 1

32. Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy

33. Brugada syndrome

35. Ventriculaire ritmestoornissen.

37. Haplotype sharing test maps genes for familial cardiomyopathies.

38. Implantable cardioverter defibrillator recipients: quality of life in recipients with and without ICD shock delivery.

41. Presymptomatisch onderzoek na plotselinge hartdood in de familie

43. Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia.

45. Recommendations and cardiological evaluation of athletes with arrhythmias: Part 2.

46. Recommendations and cardiological evaluation of athletes with arrhythmias: Part 1.

47. Implantable cardioverter defibrillator recipients: quality of life in recipients with and without ICD shock delivery: a prospective study.

48. Proposed diagnostic criteria for the Brugada syndrome.

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