A zebrafish platform for genetic and chemical screening to improve diagnosis, risk estimation and treatment of cardiovascular manifestations in Marfan syndrome.

A lifespan perspective on accelerated aging in patients with Congenital Heart Disease using clinical, (epi)genetic and inflammation markers

Doctoral project Regina Le Roux

Exploration of avenues for Precision Medicine in Heritable Thoracic Aortic Diseases

From Mice to Humans: Elucidating Cardiovascular Complications of Marfan Syndrome

TRANSITION WITH A HEART: A nurse-led multi-component transition program for adolescents with congenital heart disease - from development to evaluation

Unraveling the pathophysiology of myocardial disease in Marfan syndrome

Using a zebrafish model to improve diagnosis, risk estimation and treatment of cardiovascular manifestations of Marfan syndrome.

Contribution of immune cells to vascular wall damage and dissection in Marfan syndrome

Advancing Personalized Care in Heritable Thoracic Aortic Diseases

An integrated translational platform to improve the management and outcome of rare heritable connective tissue disease

Contribution of immune cells to vascular wall damage and dissection in Marfan syndrome

From gene to aortic dissection - detailed study of the etiology and pathogenesis and of cardiovascular characteristics of inheritable thoracic aortic aneurysms and dissections

Paving the way to precision medicine in childhood-onset diseases: A lifespan perspective on accelerated aging using the epigenetic clock

Study of the genetic basis and molecular pathogenesis of cardiovascular manifestations in heritable thoracic aortic aneurysms

Unraveling the mechanisms that drive cardiovascular manifestations in Marfan syndrome using mouse models

Using advanced fluid dynamics modelling for cardiovascular phenotyping of zebrafish models

Using Zebrafish as a novel tool to Improve the Diagnosis and Outcome of Marfan Syndrome

Aortic dissection and intramural hematoma: disruption of the biological-mechanical equilibrium?

Human stem cell-derived models to unveil mechanisms of impaired myocardial function in Marfan Syndrome