Beatrijs Bartelds

Structural and functional genomics of the CPT1B gene for muscle-type carnitine palmitoyltransferase I in mammals.

Alterations in adult rat heart after neonatal dexamethasone therapy.

Cloning and expression of the liver and muscle isoforms of ovine carnitine palmitoyltransferase 1: residues within the N-terminus of the muscle isoform influence the kinetic properties of the enzyme.

Myocardial carnitine palmitoyltransferase I expression and long-chain fatty acid oxidation in fetal and newborn lambs.

Abnormal mitochondrial bioenergetics and heart rate dysfunction in mice lacking very-long-chain acyl-CoA dehydrogenase.

Persistent pulmonary hypertension of the newborn with transposition of the great arteries.

Gene expression profile in flow-associated pulmonary arterial hypertension with neointimal lesions.

Neonatal myocardial infarction or myocarditis?

Egr-1 expression during neointimal development in flow-associated pulmonary hypertension.

Mast cell inhibition improves pulmonary vascular remodeling in pulmonary hypertension.

Differential responses of the right ventricle to abnormal loading conditions in mice: pressure vs. volume load.

Sildenafil enhances systolic adaptation, but does not prevent diastolic dysfunction, in the pressure-loaded right ventricle.

Physiological interaction of heart and lung in thoracic irradiation.

Pulsatile haemodynamic parameters are predictors of survival in paediatric pulmonary arterial hypertension.

The role of disturbed blood flow in the development of pulmonary arterial hypertension: lessons from preclinical animal models.

Distinct loading conditions reveal various patterns of right ventricular adaptation.

A cornerstone of heart failure treatment is not effective in experimental right ventricular failure.

Effect of right ventricular outflow tract obstruction on right ventricular volumes and exercise capacity in patients with repaired tetralogy of fallot.

Sildenafil add-on therapy in paediatric pulmonary arterial hypertension, experiences of a national referral centre.

Ventricular remodelling after pulmonary valve replacement: comparison between pressure-loaded and volume-loaded right ventricles.

Sildenafil treatment in established right ventricular dysfunction improves diastolic function and attenuates interstitial fibrosis independent from afterload.

A critical role for Egr-1 during vascular remodelling in pulmonary arterial hypertension.

Clinical symptoms of right ventricular failure in experimental chronic pressure load are associated with progressive diastolic dysfunction.

Echocardiography in pediatric pulmonary arterial hypertension: early study on assessing disease severity and predicting outcome.

Right ventricular failure due to chronic pressure load: What have we learned in animal models since the NIH working group statement?

Pulmonary regurgitant volume is superior to fraction using background-corrected phase contrast MRI in determining the severity of regurgitation in repaired tetralogy of Fallot.

Erythropoietin Attenuates Pulmonary Vascular Remodeling in Experimental Pulmonary Arterial Hypertension through Interplay between Endothelial Progenitor Cells and Heme Oxygenase.

The Fontan circulation and the liver: A magnetic resonance diffusion-weighted imaging study.

Egr-1 identifies neointimal remodeling and relates to progression in human pulmonary arterial hypertension.

Serially Measured Uric Acid Levels Predict Disease Severity and Outcome in Pediatric Pulmonary Arterial Hypertension.