Ghent University Academic Bibliography

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Bicuspid Aortic Valve in Heritable Thoracic Aortic Disease: Insights from the Montalcino Aortic Consortium

Kishan L. Asokan, Neha Muraly, Dongchuan Guo, Deep M. Shah, Ernesto C. Martinez, Elena Cervi, Julie De Backer (UGent) , Laura Muiño Mosquera (UGent) , Wannes Renders (UGent) , Alan C. Braverman, et al.

(2025)
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A European Delphi consensus on the management of abdominal aortic aneurysms in patients with heritable aortic diseases

Daniel Gil-Sala, Julie De Backer (UGent) , Isabelle Van Herzeele (UGent) , Gisela Teixidó-Tura, Anders Wanhainen, Sergi Bellmunt-Montoya, Nathalie Moreels (UGent) , Laura Muiño Mosquera (UGent) , Liesbeth Wildero - Van Wouwe (UGent) and [missing] Consensus Participants

(2025) EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY. 69(5). p.723-731
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Mitral annular disjunction in heritable thoracic aortic disease : insights from the Montalcino Aortic Consortium

Kishan L Asokan, Jennifer R Landes, Wannes Renders (UGent) , Laura Muiño Mosquera (UGent) , Julie De Backer (UGent) , David W Jantzen, Anji T Yetman, Gisela Teixido-Tura, Arturo Evangelista, Richmond Jeremy, et al.

(2024) JOURNAL OF THE AMERICAN HEART ASSOCIATION. 13(21).
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2024 ESC guidelines for the management of peripheral arterial and aortic diseases : developed by the task force on the management of peripheral arterial and aortic diseases of the European Society of Cardiology (ESC) endorsed by the European Association for Cardio-Thoracic Surgery (EACTS), the European Reference Network on Rare Multisystemic Vascular Diseases (VASCERN), and the European Society of Vascular Medicine (ESVM)

Lucia Mazzolai, Gisela Teixido-Tura, Stefano Lanzi, Vinko Boc, Eduardo Bossone, Marianne Brodmann, Alessandra Bura-Rivière, Julie De Backer (UGent) , Sebastien Deglise, Alessandro Della Corte, et al.

(2024) EUROPEAN HEART JOURNAL. 45(36). p.3538-3700
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HTAD patient pathway : strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) : a statement from the HTAD working group of VASCERN

Maryanne Caruana, Marieke J. Baars, Evy Bashiardes, Kalman Benke, Erik Björck, Andrei Codreanu, Elena de Moya Rubio, Julia Dumfarth, Arturo Evangelista, Maarten Groenink, et al.

(2023) EUROPEAN JOURNAL OF MEDICAL GENETICS. 66(1).
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Arrhythmia and impaired myocardial function in heritable thoracic aortic disease : an international retrospective cohort study

Anthony Demolder (UGent) , Lisa Bianco, Maryanne Caruana, Elena Cervi, Arturo Evangelista, Guillaume Jondeau, Lisa Lauren Buttigieg, Ángela López-Sainz, Elena Montañés Delmás, Alessandro Pini, et al.

(2022) EUROPEAN JOURNAL OF MEDICAL GENETICS. 65(6).
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Angiotensin receptor blockers and β blockers in Marfan syndrome : an individual patient data meta-analysis of randomised trials

Alex Pitcher, Enti Spata, Jonathan Emberson, Kelly Davies, Heather Halls, Lisa Holland, Kate Wilson, Christina Reith, Anne H Child, Tim Clayton, et al.

(2022) LANCET. 400(10355). p.822-831
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Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO

Andrea de la Fuente-Alonso, Marta Toral, Alvaro Alfayate, María Jesús Ruiz-Rodríguez, Elena Bonzón-Kulichenko, Gisela Teixido-Tura, Sara Martínez-Martínez, María José Méndez-Olivares, Dolores López-Maderuelo, Ileana González-Valdés, et al.

(2021) NATURE COMMUNICATIONS. 12(1).
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Genetic counselling and testing in adults with congenital heart disease : a consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics

Julie De Backer (UGent) , Antoine Bondue, Werner Budts, Arturo Evangelista, Pastora Gallego, Guillaume Jondeau, Bart Loeys, Maria L. Peña, Gisela Teixido-Tura, Ingrid van de Laar, et al.

(2020) EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY. 27(13). p.1423-1435
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European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

Infrid MBH van de Laar, Eloisa Arbustini, Bart Loeys, Erik Björck, Lise Murphy, Maarten Groenink, Marlies Kempers, Janneke Timmermans, Jolien Roos-Hesselink, Kalman Benke, et al.

(2019) ORPHANET JOURNAL OF RARE DISEASES. 14.

Academic Bibliography

Bicuspid Aortic Valve in Heritable Thoracic Aortic Disease: Insights from the Montalcino Aortic Consortium

A European Delphi consensus on the management of abdominal aortic aneurysms in patients with heritable aortic diseases

Mitral annular disjunction in heritable thoracic aortic disease : insights from the Montalcino Aortic Consortium

HTAD patient pathway : strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) : a statement from the HTAD working group of VASCERN

Arrhythmia and impaired myocardial function in heritable thoracic aortic disease : an international retrospective cohort study

Angiotensin receptor blockers and β blockers in Marfan syndrome : an individual patient data meta-analysis of randomised trials

Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO

Genetic counselling and testing in adults with congenital heart disease : a consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics

European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

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