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Researcher
Gunnar Buyse
- Disciplines:Orthopaedics
Affiliations
- Locomotor and Neurological Disorders (Division)
Member
From1 Jan 2019 → Today - Woman and Child (Division)
Member
From1 Apr 2013 → 31 Dec 2018
Projects
1 - 5 of 5
- Little NIRVANA 2.0: a digital multipurpose pain management system for childrenFrom1 Mar 2023 → TodayFunding: IOF - technology validation in lab
- Unlocking Therapeutic Potential: Harnessing Extracellular Vesicles and miRNAs to Combat Muscle Wasting DisordersFrom1 Apr 2020 → 26 Mar 2024Funding: BOF - doctoral mandates
- Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes to Model Chronic Cardiac DisordersFrom1 Oct 2012 → 11 Dec 2017Funding: Own budget, for example: patrimony, inscription fees, gifts
- MechDisease mechanisms, phenotypic assessments and therapy development for inherited neuromuscular disorders.From1 Oct 2010 → 30 Sep 2020Funding: Own budget, for example: patrimony, inscription fees, gifts
- Vevo 2100 micro-ultrasound machine with anesthesia platform and robotic arms for micromanipulation in small animals.From22 Jul 2010 → 21 Jan 2017Funding: Hercules - Small and Medium size research infrastructure
Publications
41 - 50 of 85
- Long-term outcome of intravesical oxybutynin in children with detrusor-sphincter dyssynergia: With special reference to age-dependent parameters(2015)
Authors: Katrien Jansen, Gunnar Buyse
Pages: 336 - 42 - Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis(2015)
Authors: Gunnar Buyse
Pages: E26 - E32 - Idebenone as a novel therapeutic approach for duchenne muscular dystrophy(2015)
Authors: Gunnar Buyse
Pages: 189 - 194 - Ataluren treatment of patients with nonsense mutation dystrophinopathy(2014)
Authors: Nathalie Goemans, Gunnar Buyse
Pages: 477 - 487 - Six minute walk test: reference values and prediction equation in healthy boys aged 5 to 12 years(2014)
Authors: Nathalie Goemans, Katrijn Klingels, M vanden Hauwe, H Feys, Gunnar Buyse
Pages: 862 - 862 - The contribution of platelet studies to the understanding of disease mechanisms in complex and monogenetic neurological disorders(2014)
Authors: Gunnar Buyse, Chris Van Geet, Kathleen Freson
Pages: 724 - 31 - Current treatment and management of dystrophinopathies(2014)
Authors: Nathalie Goemans, Gunnar Buyse
Pages: 287 - PRRT2 mutations: exploring the phenotypical boundaries(2014)
Authors: Wim Van Paesschen, Gunnar Buyse, Lieven Lagae, Kristl Claeys
Pages: 462 - 5 - Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12(2013)
Authors: Christophe Goubau, Koenraad Devriendt, Thomy de Ravel de l'Argentière, Chris Van Geet, Gunnar Buyse, Kathleen Freson
Pages: 1349 - 1355 - Another cause of hyperglyceroluria: aquaporin 7 gene mutation.(2013)
Authors: Jaak Jaeken, Christophe Goubau, Gunnar Buyse, Nathalie Goemans, Elena Levtchenko
Pages: e19