Onderzoeker
Hans De Wilde
- Trefwoorden:Geneeskunde
Affiliaties
- Pediatrie (Departement)
Lid
Vanaf1 jan 2023 → Heden - Groei en ontwikkeling (Onderzoeksgroep)
Lid
Vanaf20 okt 2022 → Heden - Pediatrie (Departement)
Lid
Vanaf1 jan 2023 → 3 jan 2024 - Pediatrie (kind) (Departement)
Lid
Vanaf1 jun 2008 → 31 dec 2022
Publicaties
1 - 10 van 18
- Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA(2022)
Auteurs: Ilse Meerschaut, Wouter Steyaert, Thierry Bové, Katrien François, Thomas Martens, katya de groote, Hans De Wilde, Laura Muiño-Mosquera, Joseph Panzer, Kristof Vandekerckhove, et al.
Pagina's: 1-12 - QRS Duration During Follow-Up of Tetralogy of Fallot(2021)
Auteurs: Thomas Martens, Katrien François, Hans De Wilde, Laurence Campens, Laurent Demulier, Julie De Backer, Daniël De Wolf, Thierry Bove
Pagina's: 1488-1495 - Paediatric subaortic stenosis(2021)
Auteurs: Rik De Wolf, Katrien François, Thierry Bové, Ilse Coomans, Katya De Groote, Hans De Wilde, Joseph Panzer, Kristof Vandekerckhove, Daniel De Wolf
Pagina's: 588-596 - A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome(2021)
Auteurs: Ilse Meerschaut, Sarah Vergult, Annelies Dheedene, Björn Menten, Katya De Groote, Hans De Wilde, Laura Muiño-Mosquera, Joseph Panzer, Kristof Vandekerckhove, Paul J Coucke, et al.
- Myocardial disease and ventricular arrhythmia in Marfan syndrome(2020)
Auteurs: Laura Muiño-Mosquera, Hans De Wilde, Daniel Devos, Danilo Babin, Luc Jordaens, Anthony Demolder, D De Wolf, Katya De Groote, Julie De Backer
- Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome(2020)
Auteurs: Aleksandra Nijak, Alain J Labro, Hans De Wilde, Wendy Dewals, Steve Peigneur, Jan Tytgat, Dirk J Snyders, Ewa Sieliwonczyk, Eline Guy S Simons, Emeline Van Craenenbroeck, et al.
- Study of the time-relationship of the mechano-electrical interaction in an animal model of tetralogy of Fallot(2020)
Auteurs: Thierry Bove, Rahi Alipour Symakani, Anne Vral, Milad El Haddad, Hans De Wilde, Roland Stroobandt, Jan De Pooter
Pagina's: 129-137 - Small-sized conduits in the right ventricular outflow tract in young children(2018)
Auteurs: Katrien François, Katya De Groote, Kristof Vandekerckhove, Hans De Wilde, Daniël De Wolf, Thierry Bové
Pagina's: 409-415 - Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes(2017)
Auteurs: 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, et al.
- Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies(2017)
Auteurs: Katya De Groote, Ellen Vanhie, Ellen Roets, Paul Ramaekers, Hans De Wilde, Joseph Panzer, Kristof Vandekerckhove, Thierry Bove, Katrien François, Koen Van Herck
Pagina's: 983-991