Ghent University Academic Bibliography

Your filters: cql: author="Evangelista, Arturo" or (type any "bookEditor issueEditor" and editor="Evangelista, Arturo")

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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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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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Comparative risks of initial aortic events associated with genetic thoracic aortic disease

Ellen S. Regalado, Shaine A. Morris, Alan C. Braverman, Ellen M. Hostetler, Julie De Backer (UGent) , Ruosha Li, Reed E. Pyeritz, Anji T. Yetman, Elena Cervi, Sherene Shalhub, et al.

(2022) JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. 80(9). p.857-869
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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.
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False lumen flow patterns and their relation with morphological and biomechanical characteristics of chronic aortic dissections : computational model compared with magnetic resonance imaging measurements

Paula A Rudenick, Patrick Segers (UGent) , Victor Pineda, Hug Cuellar, David García-Dorado, Arturo Evangelista and Bart H Bijnens

(2017) PLOS ONE. 12(1).
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Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome

Jorge Oller, Nerea Méndez-Barbero, E Josue Ruiz, Silvia Villahoz, Marjolijn Renard (UGent) , Lizet I Canelas, Ana M Briones, Rut Alberca, Noelia Lozano-Vidal, María A Hurlé, et al.

(2017) NATURE MEDICINE. 23(2). p.200-212

Academic Bibliography

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

Comparative risks of initial aortic events associated with genetic thoracic aortic disease

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

False lumen flow patterns and their relation with morphological and biomechanical characteristics of chronic aortic dissections : computational model compared with magnetic resonance imaging measurements

Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome

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