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Expert Review of Cardiovascular Therapy|May 23, 2015
Managing aortic aneurysms and dissections during pregnancyLaura Muiño Mosquera, Julie De Backer
Frontiers in Pediatrics|August 2, 2021
Cardiomyopathy in Genetic Aortic DiseasesLaura Muiño-Mosquera, Julie De Backer
Revista Espanola De Cardiologia (English Ed.)|July 11, 2020
Genetics in congenital heart disease. Are we ready for it?Julie De Backer, Bert Callewaert, Laura Muiño Mosquera
Molecular Genetics & Genomic Medicine|November 16, 2024
Assessment of Myocardial Fibrosis in Marfan Syndrome Using Cardiac Magnetic Resonance ImagingAnthony Demolder, Dan Devos, Julie De Backer, et al.
Diagnostics (Basel, Switzerland)|September 30, 2020
Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature ReviewAnthony Demolder, Yskert von Kodolitsch, Laura Muiño-Mosquera, et al.
JAMA Cardiology|July 7, 2021
Association of Mitral Annular Disjunction With Cardiovascular Outcomes Among Patients With Marfan SyndromeAnthony Demolder, Frank Timmermans, Mattias Duytschaever, et al.
European Journal of Pediatrics|June 23, 2023
Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stageMichèle de Hosson, Katya De Groote, Herlinde Wynendaele, et al.
Acta Cardiologica|June 29, 2017
Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trialLaura Muiño-Mosquera, Sylvia De Nobele, Daniel Devos, et al.
Stem Cell Research|February 1, 2023
Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editingJeffrey Aalders, Laurens Léger, Anthony Demolder, et al.
Orphanet Journal of Rare Diseases|February 4, 2015
Gene panel sequencing in heritable thoracic aortic disorders and related entities - results of comprehensive testing in a cohort of 264 patientsLaurence Campens, Bert Callewaert, Laura Muiño Mosquera, et al.
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