Researcher
Liesbeth De Waele
- Disciplines:Orthopaedics
Affiliations
- Locomotor and Neurological Disorders (Division)
Member
From1 Nov 2020 → Today - Woman and Child (Division)
Member
From1 Nov 2020 → 9 Nov 2020 - Development and Regeneration, Kulak Kortrijk Campus (Department)
Member
From1 Oct 2013 → 31 Oct 2020 - Centre for Molecular and Vascular Biology (Division)
Member
From1 Oct 2003 → 30 Sep 2005
Projects
1 - 4 of 4
- Development, Validation, and Valorization of a Patient Preference Platform to Inform Healthcare Decision-MakingFrom1 Mar 2023 → TodayFunding: IOF - technology validation in lab
- Computer-aided orthosis design to improve walking performance in children with Duchenne muscular distrophy and cerebral palsyFrom1 Jan 2022 → TodayFunding: FWO research project (including WEAVE projects)
- Unlocking Therapeutic Potential: Harnessing Extracellular Vesicles and miRNAs to Combat Muscle Wasting DisordersFrom1 Apr 2020 → 26 Mar 2024Funding: BOF - doctoral mandates
- Understanding and management of neurobehavioral difficulties in patients with Duchenne Muscular DystrophyFrom1 Oct 2018 → 1 Oct 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
Publications
51 - 60 of 78
- Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts(2017)
Authors: David Cassiman, Liesbeth De Waele, Lieven Lagae, Hilde Van Esch
Pages: 317 - Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts(2016)
Authors: David Cassiman, Liesbeth De Waele, Lieven Lagae, Hilde Van Esch
Pages: 1185 - 1192 - EFFECTS: an expanded access program of everolimus for patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex(2016)
Authors: Liesbeth De Waele
- CEREBELLAR MUTISM SYNDROME IN POSTERIOR FOSSA TUMORS: A BETTER UNDERSTANDING FOR A BETTER COUNSELING. A RETROSPECTIVE ANALYSIS OF PEDIATRIC PATIENTS IN UZ LEUVEN FROM 1990 TO 2015(2016)
Authors: Lien Mertens, Liesbeth De Waele, Bart Depreitere, Jurgen Lemiere, Sandra Jacobs
Pages: 16 - 16 - Increased Understanding of Stem Cell Behavior in Neurodegenerative and Neuromuscular Disorders by Use of Noninvasive Cell Imaging(2016)
Authors: Bryan Holvoet, Liesbeth De Waele, Mattia Quattrocelli, Olivier Gheysens, Maurilio Sampaolesi, Catherine Verfaillie, Christophe Deroose
Pages: 6235687 - 6235687 - Tuberous sclerosis complex: the past and the future(2015)
Authors: Liesbeth De Waele, Lieven Lagae, Djalila Mekahli
Pages: 1771 - 80 - Tuberous sclerosis complex: the past and the future(2015)
Authors: Liesbeth De Waele, Lieven Lagae, Djalila Mekahli
Pages: 1771 - 80 - Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1(2015)
Authors: Liesbeth De Waele, Koenraad Devriendt, Lieven Lagae, Luc Régal
Pages: 296 - 312 - Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1(2015)
Authors: Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, Marcin Szynkiewicz, Gabriella M A Forte, Hannah L Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, et al.
Pages: 296 - 312 - Charcot-Marie-Tooth: are you testing for proteinuria?(2015)
Authors: Stéphanie De Rechter, Liesbeth De Waele, Elena Levtchenko, Djalila Mekahli
Pages: 1 - 5