47 results on '"Mulder, Barbara Jm"'
Search Results
2. Contemporary survival of adults with congenital heart disease
3. Individualised prediction of pulmonary homograft durability in tetralogy of Fallot
4. 2020 ESC Guidelines for the management of adult congenital heart disease The Task Force for the management of adult congenital heart disease of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Adult Congenital Heart Disease (ISACHD)
5. The Effect of Resveratrol on Aortic Function in Patients with Marfan Syndrome – Rationale and Design of the Resvcue Marfan Trial.
6. Final comment on the debate article “ICD implantation as primary prevention in systemic RV”
7. Serial follow-up of biventricular function, exercise capacity and NT-proBNP measurements in repaired tetralogy of Fallot: is there a role for MR stress imaging?
8. Intra-observer and interobserver variability of biventricular function, volumes and mass in patients with congenital heart disease measured by CMR imaging
9. Surgical versus percutaneous treatment of aortic coarctation: new standards in an era of transcatheter repair
10. Adults with congenital heart disease: Patients’ knowledge and concerns about inheritance
11. Opportunities in pulmonary valve replacement
12. Non-vitamin K antagonist oral anticoagulants in adults with a Fontan circulation: are they safe
13. C Identification of the major genetic contributors to tetralogy of fallot
14. Renal cystic disease in the Fbn1C1039G/+ Marfan mouse is associated with enhanced aortic aneurysm formation
15. Losartan therapy in adults with Marfan syndrome: study protocol of the multi-center randomized controlled COMPARE trial
16. Evaluating the systemic right ventricle by CMR: the importance of consistent and reproducible delineation of the cavity
17. Aortic microcalcification is associated with elastin fragmentation in Marfan syndrome
18. A propensity score-adjusted analysis of clinical outcomes after pulmonary valve replacement in tetralogy of Fallot
19. Chance of surgery in adult congenital heart disease
20. Aortopathies in adult congenital heart disease and genetic aortopathy syndromes: management strategies and indications for surgery
21. Clinical and psychological characteristics predict future healthcare use in adults with congenital heart disease
22. Management of Pregnancy in Marfan Syndrome, Ehlers–Danlos Syndrome and Other Heritable Connective Tissue Disorders
23. Diagnosis and genetics of Marfan syndrome
24. A propensity score-adjusted analysis of clinical outcomes after pulmonary valve replacement in tetralogy of Fallot
25. Illness perceptions of adults with congenital heart disease and their predictive value for quality of life two years later
26. Erratum
27. Patients with a congenital heart defect and Type D personality feel functionally more impaired, report a poorer health status and quality of life, but use less healthcare
28. Current and future pharmacological treatment strategies with regard to aortic disease in Marfan syndrome
29. Treatment of Congenital Heart Disease: risk-reducing Measures in Young Adults
30. Serial follow-up of biventricular function, exercise capacity and NT-proBNP measurements in repaired tetralogy of Fallot: is there a role for MR stress imaging?
31. ALK2 mutation in a patient with Down's syndrome and a congenital heart defect
32. Interventional and surgical treatment of cardiac arrhythmias in adults with congenital heart disease
33. DOPPLER ECHOCARDIOGRAPHY AFTER BENTALL PROCEDURE COMPARED TO AN ISOLATED AORTIC VALVE PROSTHESES
34. AORTIC DISTENSIBILITY IS A PREDICTOR FOR AORTIC EVENTS IN PATIENTS WITH MARFAN SYNDROME: A 12 YEAR-SURVIVAL ANALYSIS
35. ATHEROSCLEROSIS PROGRESSION IN ADULT POST-COARCTECTOMY PATIENTS
36. Atherosclerosis in Patients With Cyanotic Congenital Heart Disease
37. Intra-observer and interobserver variability of biventricular function, volumes and mass in patients with congenital heart disease measured by CMR imaging
38. Bosentan in mild pulmonary hypertension
39. Evaluating the systemic right ventricle by CMR: the importance of consistent and reproducible delineation of the cavity
40. Relation between exercise-induced hypertension and sustained hypertension in adult patients after successful repair of aortic coarctation
41. The potential role of plasma neurohormones in the follow-up of unoperated or physiologically repaired congenitally corrected transposition of the great arteries
42. Illness perceptions of adults with congenital heart disease and their predictive value for quality of life two years later.
43. Individualised prediction of pulmonary homograft durability in tetralogy of Fallot.
44. Renal cystic disease in the Fbn1 C1039G/+ Marfan mouse is associated with enhanced aortic aneurysm formation.
45. Current state of risk stratification for sudden cardiac death in adults with congenital heart disease.
46. Aortic microcalcification is associated with elastin fragmentation in Marfan syndrome.
47. Adult patients with pulmonary arterial hypertension due to congenital heart disease: a review on advanced medical treatment with bosentan.
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