Researcher
Laura Muino Mosquera
- Keywords:Medicine
Affiliations
- Pediatrics (Department)
Member
From17 Mar 2020 → 15 Mar 2021 - Pediatrics (Department)
Member
From17 Mar 2020 → 15 Mar 2021 - Pediatrics (Department)
Member
From1 Aug 2011 → 29 Oct 2013
Publications
1 - 8 of 8
- Evaluation of a nurse-led multi-component transition program for adolescents with congenital heart disease(2024)
Authors: Michèle de Hosson, katya de groote, Ann Van Hecke, D De Wolf, Kristof Vandekerckhove, Laura Muiño-Mosquera, Joseph Panzer, Karen Logghe, Saskia Mels, Laurent Demulier, et al.
- Evaluation of late cardiac effects after multisystem inflammatory syndrome in children(2023)
Authors: Rik De Wolf, Mahmoud Zaqout, Kaoru Tanaka, Laura Muiño-Mosquera, Gerlant van Berlaer, Kristof Vandekerckhove, Wendy Dewals, D De Wolf
- Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA(2022)
Authors: 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.
Pages: 1-12 - A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome(2021)
Authors: 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.
- More than meets the eye(2021)
Authors: Tibbe Dhooge, Tim Van Damme, Delfien Syx, Laura Muiño-Mosquera, Sheela Nampoothiri, Anil Radhakrishnan, Pelin Ozlem Simsek-Kiper, Gülen Eda Utine, Maryse Bonduelle, Isabelle Migeotte, et al.
Pages: 711-730 - Myocardial disease and ventricular arrhythmia in Marfan syndrome(2020)
Authors: Laura Muiño-Mosquera, Hans De Wilde, Daniel Devos, Danilo Babin, Luc Jordaens, Anthony Demolder, D De Wolf, Katya De Groote, Julie De Backer
- Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline(2018)
Authors: Laura Muiño-Mosquera, Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Anne De Paepe, Wouter Steyaert, Sofie Symoens, Paul Coucke, Bert Callewaert, Marjolijn Renard, et al.
- Analysis of the recovery phase after maximal exercise in children with repaired tetralogy of Fallot and the relationship with ventricular function
Authors: Ilse Coomans, Sara De Kinder, Hannah Van Belleghem, Katya De Groote, Joseph Panzer, Hans De Wilde, Laura Muiño-Mosquera, Katrien François, Thierry Bove, Thomas Martens, et al.
Pages: e0244312