US
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice | Journal of medical genetics |  | 2011 | 676 | 0 | ||
| Incidence of atrial fibrillation after percutaneous closure of patent foramen ovale and small atrial septal defects in patients presenting with cryptogenic stroke | European journal of cardiovascular prevention & rehabilitation | | 2010 | 616 | 0 | ||
| A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy | Human mutation | | 2008 | 758 | 0 | ||
| The role of the sizing balloon in selection of the patent foramen ovale closure device size | Experimental and clinical cardiology | | 2008 | 643 | 0 | ||
| Coronary myocardial bridge: an innocent bystander? | Heart and vessels |  | 2008 | 709 | 317 | ||
| Percutaneous closure of a residual ventricular septal defect in a challenging patient | Acute cardiac care | | 2006 | 466 | 0 | ||
| L'apport de la génétique moléculaire en cardiologie clinique : l'exemple de la cardiomyopathie hypertrophique | Revue médicale suisse | | 2005 | 577 | 1 | ||
| Prise en charge de l'insuffisance cardiaque terminale | Revue médicale suisse | | 2005 | 507 | 0 |
