Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report by Aleksandra Nijak, Alain J. Labro, Hans De Wilde, Hans De Wilde, Wendy Dewals, Steve Peigneur, Jan Tytgat, Dirk Snyders, Ewa Sieliwonczyk, Eline Simons, Emeline Van Craenenbroeck, Dorien Schepers, Lut Van Laer, Johan Saenen, Bart Loeys, Bart Loeys, Maaike Alaerts

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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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Different Patterns of Cerebral and Muscular Tissue Oxygenation 10 Years After Coarctation Repair by Kristof Vandekerckhove, Joseph Panzer, Ilse Coomans, Annelies Moerman, Katya De Groote, Hans De Wilde, Thierry Bové, Katrien François, Daniel De Wolf, Jan Boone

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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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Analysis of the recovery phase after maximal exercise in children with repaired tetralogy of Fallot and the relationship with ventricular function. by Ilse Coomans, Sara De Kinder, Hannah Van Belleghem, Katya De Groote, Joseph Panzer, Hans De Wilde, Laura Muiño Mosquera, Katrien François, Thierry Bové, Thomas Martens, Daniël De Wolf, Jan Boone, Kristof Vandekerckhove

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Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes by Delfien J. Bogaert, Melissa Dullaers, Hye Sun Kuehn, Bart P. Leroy, Julie E. Niemela, Hans De Wilde, Sarah De Schryver, Marieke De Bruyne, Frauke Coppieters, Bart N. Lambrecht, Frans De Baets, Sergio D. Rosenzweig, Elfride De Baere, Filomeen Haerynck

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