21 results on '"Mulder, Barbara J. M."'
Search Results
2. Histopathology of aortic complications in bicuspid aortic valve versus Marfan syndrome: relevance for therapy?
3. Losartan versus atenolol in the Marfan aorta—how to treat?
4. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
5. The Clinical and Molecular Relations Between Idiopathic Preterm Labor and Maternal Congenital Heart Defects
6. Right ventricular function declines after cardiac surgery in adult patients with congenital heart disease
7. A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q
8. The changing epidemiology of congenital heart disease
9. Intra-observer and interobserver variability of biventricular function, volumes and mass in patients with congenital heart disease measured by CMR imaging
10. Prevalence of congenital heart defects in neuroblastoma patients: a cohort study and systematic review of literature
11. Tetralogy of Fallot: in good shape?
12. Duchenne muscular dystrophy; a cardiomyopathy that can be prevented?
13. Interpretation Bias for Heart Sensations in Congenital Heart Disease and its Relation to Quality of Life
14. Diastolic dysfunction: a new additional criterion for optimal timing of pulmonary valve replacement in adult patient with tetralogy of Fallot?
15. Is fatigue in Marfan syndrome related to orthostatic intolerance?
16. Genes in congenital heart disease: atrioventricular valve formation
17. Cardiovascular magnetic resonance in a pregnant patient with absent pulmonary valve syndrome
18. Intracardiac echocardiography. A new tool in the cath lab
19. CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: Rationale, design, and first results
20. Cardiac imaging in the digital era: how can the technicians help us further
21. Heartbeat sensitivity in adults with congenital heart disease
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