prof. dr. Julie De Backer
- ORCID iD
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0000-0001-8878-1507
- Bio (via ORCID)
- Julie De Backer is a cardiologist and clinical geneticist with a clinical and research interest in Heritable Thoracic Aortic Diseases (HTAD) and Adult Congenital Heart Disease (ACHD) working at the Ghent University Hospital in Belgium. She focuses on deep cardiovascular phenotyping in Marfan syndrome and related disorders and the relation to the genotype. Using genetically engineered animal models she and her team aim to identify new targets for better treatment and management. She is also involved in several multidisciplinary clinics for patients with HTAD and ACHD and in the development of adequate transition programs for these patients. She is an active member of several consortia and international societies in the field, including the European Reference Network for Rare Multisystemic Vasculair Disease and the Montalcino Aortic Consortium.
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The ‘Ten Commandments’ for the 2025 ESC Guidelines on Cardiovascular Disease and Pregnancy
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- Journal Article
- A1
- open access
Preventing cardiovascular complications in adults with congenital heart disease : predictors and outcomes of the levels of follow-up care
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Translating the latest 2025 ESC guidelines and consensus statement into acute cardiovascular care practice
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2025 ESC guidelines for the management of cardiovascular disease and pregnancy : developed by the task force on the management of cardiovascular disease and pregnancy of the European Society of Cardiology (ESC) endorsed by the European Society of Gynecology (ESG)
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The challenges of decision-making in managing women with prosthetic heart valves during pregnancy : a global concern
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- Journal Article
- A1
- open access
Perceived health, psychological distress and quality of life in 8415 adults with congenital heart disease from 32 countries
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- Journal Article
- A1
- open access
Novel aortic dissection model links endothelial dysfunction and immune infiltration
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- Journal Article
- A1
- open access
Differences in arterial events in vascular Ehlers-Danlos, Loeys-Dietz, and Marfan syndrome
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- Journal Article
- A1
- open access
Pregnancy outcomes in women with heritable thoracic aortic disease : data from the EORP ESC Registry of Pregnancy and Cardiac disease (ROPAC) III
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- Journal Article
- A1
- open access
Valve-sparing root replacement in bicuspid and tricuspid aortic valves : long-term outcomes into the second decade