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Researcher
Veerle Labarque
- Disciplines:Cardiac and vascular medicine, Molecular and cell biology
Affiliations
- Centre for Molecular and Vascular Biology (Division)
Member
From1 Oct 2005 → Today
Projects
1 - 7 of 7
- Whole genome and RNA sequencing for platelet disordersFrom3 Nov 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Improved disease modelling and genetics for inherited platelet disordersFrom1 Oct 2021 → TodayFunding: FWO fellowships
- Withholding/withdrawing life sustaining treatment in pediatrics: an ethical analysisFrom22 Feb 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Improved disease modelling and genetics for inherited platelet disordersFrom1 Jan 2021 → TodayFunding: FWO research project
- Mechanism of podocyte damage in the development of sickle cell nephropathyFrom1 Nov 2019 → TodayFunding: FWO fellowships, BOF - doctoral mandates
- Management of Kidney diseases in Sickle Cell children in Belgium and in the Democratic Republic of CongoFrom14 Oct 2019 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Genome medicine for bleeding, thrombotic and platelet disordersFrom1 Oct 2019 → TodayFunding: BOF - projects
Publications
1 - 10 of 47
- Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study(2022)
Authors: Veerle Labarque, Christel Van Geet, Kathelijne Peerlinck, Kathleen Freson
Pages: E248 - E250 - Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence(2022)
Authors: Alice Cavolo, Veerle Labarque, Chris Gastmans
- HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia(2022)
Authors: Kim De Keersmaecker, Veerle Labarque
Pages: 3111 - 3126 - Long-Term Outcome of Single-Session, Ultrasound-Guided, Radiofrequency Ablation for Symptomatic Small, Lower Limb, Venous Malformations.(2022)
Authors: Veerle Labarque, Inge Fourneau, Geert Maleux
Pages: 68 - Hemostatic phenotypes and genetic disorders(2021)
Authors: Fabienne Ver Donck, Veerle Labarque, Kathleen Freson
- F11 Gene Duplication Causes Elevated FXI Plasma Levels and Is a Risk for Venous Thrombosis(2021)
Authors: Kathelijne Peerlinck, Marc Jacquemin, Veerle Labarque, Kathleen Freson
Pages: 1 - 3 - Clinical and genetic factors are associated with kidney complications in African children with sickle cell anaemia(2021)
Authors: Oyindamola Christiana Adebayo, Lambertus van den Heuvel, Elena Levtchenko, Veerle Labarque
Pages: 204 - 214 - Spontaneous intracranial haemorrhage as initial presentation of haemophilia in infants and children: A case report and systematic literature review(2021)
Authors: Veerle Labarque
Pages: E398 - E401 - Methylene tetrahydrofolate reductase A1298C polymorphisms influence the adult sequelae of chemotherapy in childhood-leukemia survivors(2021)
Authors: Sabine Deprez, Charlotte Sleurs, Veerle Labarque, Anne Uyttebroeck, Jurgen Lemiere, Rudi D'Hooge
Pages: 1 - 13 - Subconjunctival Hemorrhage in a Child with the Blue Rubber Bleb Nevus Syndrome on Treatment with Oral Propranolol(2021)
Authors: Veerle Labarque, Ingele Casteels
Pages: 451 - 456