| | Title | Authors / Editors | Date |
|
unige:34666 |
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice |
Fokstuen, Siv; Munoz, Analia; Melacini, Paola; Iliceto, Sabino; ... Blouin, Jean-Louis |
2011 |
|
unige:19696 |
Incidence of atrial fibrillation after percutaneous closure of patent foramen ovale and small atrial septal defects in patients presenting with cryptogenic stroke |
Bonvini, Robert; Sztajzel, Roman; Dorsaz, Pierre-André; Righini, Marc Philip; ... Sztajzel, Juan |
2010 |
|
unige:1810 |
The role of the sizing balloon in selection of the patent foramen ovale closure device size |
Alibegovic, Jasmina; Bonvini, Robert; Sigwart, Ulrich; Dorsaz, P A.; ... Verine, Vitali |
2008 |
|
unige:872 |
Coronary myocardial bridge: an innocent bystander? |
Bonvini, Robert; Alibegovic, Jasmina; Perret, Xavier; Keller, Pierre-Frédéric; ... Sigwart, Ulrich |
2008 |
|
unige:1055 |
A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy |
Fokstuen, Siv; Lyle, Robert; Munoz, Analia; Gehrig, Corinne; ... Blouin, Jean-Louis |
2008 |
|
unige:54910 |
Percutaneous closure of a residual ventricular septal defect in a challenging patient |
Aitsiselmi, Amina; Bonvini, Robert F; Aggoun, Yacine; Sigwart, Ulrich |
2006 |
|
unige:9174 |
L'apport de la génétique moléculaire en cardiologie clinique : l'exemple de la cardiomyopathie hypertrophique |
Fokstuen, Siv; Blouin, Jean-Louis; Lyle, Robert; Lerch, René; ... Sigwart, Ulrich |
2005 |
|
unige:39524 |
Prise en charge de l’insuffisance cardiaque terminale |
Schnetzler, Bruno; Reverdin, Stéphane; Sunthorn, Henri; Kalangos, Afksendiyos; Sigwart, Ulrich |
2005 |
Sigwart, Ulrich
add all
remove all
