Laurence Campens
- ORCID iD
- 0000-0002-5045-2449
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- Journal Article
- A1
- open access
Multimodality 3D image fusion with live fluoroscopy reduces radiation dose during catheterization of congenital heart defects
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Evaluation of a nurse-led multi-component transition program for adolescents with congenital heart disease
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- Journal Article
- open access
Serum calcification propensity T50 associates with disease severity in patients with pseudoxanthoma elasticum
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- Journal Article
- A2
- open access
The coronavirus disease pandemic among adult congenital heart disease patients and the lessons learnt : results of a prospective multicenter European registry
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- Journal Article
- A1
- open access
The hammock sign in computed tomography as a detection aid for bicuspid aortic valves
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How to measure the aorta in the setting of genetic aortic disease
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Aortic annulus S-curve : implications for transcatheter aortic valve replacement and related procedures, part 1
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Calcium-induced infolding of a self-expanding transcatheter aortic valve in type 1 bicuspid aortic valve stenosis
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- Journal Article
- A1
- open access
Serum calcification propensity T50 associates with disease severity in patients with pseudoxanthoma elasticum
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Clinical and subclinical findings in heterozygous ABCC6 carriers : results from a Belgian cohort and clinical practice guidelines
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- Journal Article
- A1
- open access
Clinical outcome of COVID-19 in patients with adult congenital heart disease
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- Journal Article
- A1
- open access
Propionyl-L-carnitine for intermittent claudication
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QRS duration during follow-up of tetralogy of fallot : how valuable is it? Analysis of ECG changes in relation to pulmonary valve implantation
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- Journal Article
- A1
- open access
Pregnancy outcome in thoracic aortic disease data from the Registry Of Pregnancy And Cardiac disease
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- Journal Article
- A1
- open access
MEK1/2 inhibition in murine heart and aorta after oral administration of refametinib supplemented drinking water
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A new dimension in patent foramen ovale size estimation
(2020) ECHOCARDIOGRAPHY - A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES. 37(7). p.1049-1055 -
Marfan syndrome
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Looking for the missing links : challenges in the search for genotype-phenotype correlation in Marfan syndrome
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Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome : a randomized, double-blind clinical trial
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Dissection of genotypic and cardiovascular phenotypic features of heritable connective tissue disorders
(2016) -
Marfan syndrome and related heritable thoracic aortic aneurysms and dissections
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Intrinsic cardiomyopathy in Marfan syndrome: results from in- and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans
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- Journal Article
- A1
- open access
Gene panel sequencing in heritable thoracic aortic disorders and related entities: results of comprehensive testing in a cohort of 264 patients
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Propionyl-L-carnitine for intermittent claudication: a cochrane review
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Mutation detection rate and - characteristics in thoracic aortic aneurysm (TAA) related disorders: results from next generation sequencing (NGS) panel testing
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Reference values for echocardiographic assessment of the diameter of the aortic root and ascending aorta spanning all age categories
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Een expeditie stroomafwaarts uit het linkerventrikel: verslag van het Lentesymposium georganiseerd door het Hartcentrum UZ Gent en de Dienst Cardiologie UZ Antwerpen op 21 maart 2013, Gent
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- Journal Article
- A1
- open access
Absence of cardiovascular manifestations in a haploinsufficient TGFBR1 mouse model
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New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections
(2013) POLSKIE ARCHIWUM MEDYCYNY WEWNETRZNEJ-POLISH ARCHIVES OF INTERNAL MEDICINE. 123(12). p.693-700 -
Marfan related cardiomyopathy: an in vivo and in vitro study of the fbn1C1039G/+ mouse model
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Normal values for ascending aortic diameters with 2D echocardiography
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Screening en beleid bij erfelijke thoracale aorta aneurysmata en dissecties
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Characterization of cardiovascular involvement in pseudoxanthoma elasticum families
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Mechanische kleppen en anticoagulatie tijdens de zwangerschap
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Genes in thoracic aortic aneurysms/dissections : do they matter?
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Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2
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- Journal Article
- A1
- open access
Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD
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Impaired vascular elasticity and diastolic dysfunction in pseudoxanthoma elasticum
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Impaired vascular elasticity and diastolic dysfunction in pseudoxanthoma elasticum
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Accuracy of oscillometric determination of the ankle-brachial index as screening method for peripheral artery disease
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Propionyl-L-carnitine for intermittent claudication (protocol)
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Erfelijke vormen van thoracale aorta-aneurysma's en -dissecties : diagnostiek en beleid
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Left ventricular dysfunction in a mouse model of Marfan syndrome
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Oorzaken en behandeling van aortadilatatie bij het bicuspide-aortaklepsyndroom