Cardiomyopathy in Genetic Aortic Diseases by Laura Muiño-Mosquera, Laura Muiño-Mosquera, Julie De Backer, Julie De Backer

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Editorial: Women in pediatric cardiology 2021 by Laura Muiño-Mosquera, Sarah Nordmeyer

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Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review by Anthony Demolder, Yskert von Kodolitsch, Laura Muiño-Mosquera, Julie De Backer

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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... by Jeffrey Aalders, Laurens Léger, Anthony Demolder, Laura Muiño Mosquera, Paul Coucke, Björn Menten, Julie De Backer, Jolanda van Hengel

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Sex, pregnancy and aortic disease in Marfan syndrome. by Marjolijn Renard, Laura Muiño-Mosquera, Elise C Manalo, Sara Tufa, Eric J Carlson, Douglas R Keene, Julie De Backer, Lynn Y Sakai

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Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study by Laura Muiño-Mosquera, Hans De Wilde, Daniel Devos, Danilo Babin, Luc Jordaens, Anthony Demolder, Katya De Groote, Daniel De Wolf, Julie De Backer

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Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome by Laura Muiño‐Mosquera, Fré Bauters, Karlien Dhondt, Hans De Wilde, Luc Jordaens, Katya De Groote, Daniel De Wolf, Katrien Hertegonne, Julie De Backer

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Evaluation of late cardiac effects after multisystem inflammatory syndrome in children by Rik De Wolf, Mahmoud Zaqout, Mahmoud Zaqout, Kaoru Tanaka, Laura Muiño-Mosquera, Gerlant van Berlaer, Kristof Vandekerckhove, Wendy Dewals, Daniël De Wolf, Daniël De Wolf

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Physical activity and physical fitness in children with heritable connective tissue disorders by Lisanne de Koning, Lisanne de Koning, Jessica Warnink-Kavelaars, Jessica Warnink-Kavelaars, Marion van Rossum, Marion van Rossum, Selina Limmen, Ruth Van der Looven, Laura Muiño-Mosquera, Laura Muiño-Mosquera, Annelies van der Hulst, Jaap Oosterlaan, Jaap Oosterlaan, Lies Rombaut, Raoul Engelbert, Raoul Engelbert, Raoul Engelbert, on behalf of the Pediatric Heritable Connective Tissue Disorders Study Group

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A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome by Ilse Meerschaut, Sarah Vergult, Annelies Dheedene, Björn Menten, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Kristof Vandekerckhove, Paul J. Coucke, Daniël De Wolf, Bert Callewaert

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Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA by Ilse Meerschaut, Wouter Steyaert, Thierry Bové, Katrien François, Thomas Martens, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Kristof Vandekerckhove, Lara Moons, Petra Vermassen, Sofie Symoens, Paul J. Coucke, Daniël De Wolf, Bert Callewaert

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P150: ClinGen hereditary cardiovascular disease gene curation expert panel: reappraisal of the validity of hypertrophic cardiomyopathy genes* by Amber Waddell, Sophie Hespe, Babken Asatryan, Emma Owens, Courtney Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily Brown, Lily Hoffman-Andrews, Elizabeth Jordan, Megan Mayers, Stacey Peters, Fergus Stafford, Richard Bagnall, Lucas Bronicki, Bert Callewaert, C. Anwar Chahal, Cynthia James, Olga Jarinova, Andrew Landstrom, Elizabeth McNally, Brittney Murray, Laura Muiño-Mosquera, Victoria Parikh, Chloe Reuter, Roddy Walsh, Bess Wayburn, James Ware, Jodie Ingles

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