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Veerle Labarque

Showing results (51-60 of 76) with videos related to

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Blood|July 28, 2019
Genetic determinants of VWF clearance and FVIII binding modify FVIII pharmacokinetics in pediatric hemophilia A patientsLaura L Swystun, Kenichi Ogiwara, Orla Rawley, et al.
Journal of Thrombosis and Haemostasis : JTH|May 28, 2025
Genotype vs laboratory phenotype correlation of defects in natural anticoagulants in patients with venous thromboembolismChristine Van Laer, Marthe Vanrenterghem, Marc Jacquemin, et al.
The Journal of Clinical Endocrinology and Metabolism|September 25, 2008
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in plateletsKathleen Freson, Benedetta Izzi, Veerle Labarque, et al.
Journal of Thrombosis and Haemostasis : JTH|January 12, 2025
Multigene panel for thrombophilia testing in venous thromboembolismAndreas Verstraete, Mae Jeraldine De Vera, Christine Van Laer, et al.
Pediatric Nephrology (Berlin, Germany)|March 28, 2024
Estimated glomerular filtration rate: applicability of creatinine-based equations in African childrenAgathe Bikupe Nkoy, Therance Tobo Matoka, Justine Busanga Bukabau, et al.
Plos One|June 9, 2012
Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunctionBenedetta Izzi, Inge Francois, Veerle Labarque, et al.
Research and Practice in Thrombosis and Haemostasis|April 17, 2025
Clinical utility of panel-based genetic sequencing for von Willebrand diseaseRadha Ramanan, Christine Van Laer, Sarissa Baert, et al.
Blood|January 22, 2025
Functional assessment of genetic variants in thrombomodulin detected in patients with bleeding and thrombosisChristine Van Laer, Renaud Lavend'homme, Sarissa Baert, et al.
Journal of Thrombosis and Haemostasis : JTH|May 12, 2026
Inhibitor development according to FVIII concentrates in PUPs with severe hemophilia A: update from the PedNet registryKathelijn Fischer, Martin Olivieri, Susanna Ranta, et al.
British Journal of Haematology|June 27, 2024
Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemiaAgathe B Nkoy, Floreen M Mumaka, Ange Ngonde, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Blood|July 28, 2019
Genetic determinants of VWF clearance and FVIII binding modify FVIII pharmacokinetics in pediatric hemophilia A patientsLaura L Swystun, Kenichi Ogiwara, Orla Rawley, et al.
Journal of Thrombosis and Haemostasis : JTH|May 28, 2025
Genotype vs laboratory phenotype correlation of defects in natural anticoagulants in patients with venous thromboembolismChristine Van Laer, Marthe Vanrenterghem, Marc Jacquemin, et al.
The Journal of Clinical Endocrinology and Metabolism|September 25, 2008
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in plateletsKathleen Freson, Benedetta Izzi, Veerle Labarque, et al.
Journal of Thrombosis and Haemostasis : JTH|January 12, 2025
Multigene panel for thrombophilia testing in venous thromboembolismAndreas Verstraete, Mae Jeraldine De Vera, Christine Van Laer, et al.
Pediatric Nephrology (Berlin, Germany)|March 28, 2024
Estimated glomerular filtration rate: applicability of creatinine-based equations in African childrenAgathe Bikupe Nkoy, Therance Tobo Matoka, Justine Busanga Bukabau, et al.
Plos One|June 9, 2012
Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunctionBenedetta Izzi, Inge Francois, Veerle Labarque, et al.
Research and Practice in Thrombosis and Haemostasis|April 17, 2025
Clinical utility of panel-based genetic sequencing for von Willebrand diseaseRadha Ramanan, Christine Van Laer, Sarissa Baert, et al.
Blood|January 22, 2025
Functional assessment of genetic variants in thrombomodulin detected in patients with bleeding and thrombosisChristine Van Laer, Renaud Lavend'homme, Sarissa Baert, et al.
Journal of Thrombosis and Haemostasis : JTH|May 12, 2026
Inhibitor development according to FVIII concentrates in PUPs with severe hemophilia A: update from the PedNet registryKathelijn Fischer, Martin Olivieri, Susanna Ranta, et al.
British Journal of Haematology|June 27, 2024
Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemiaAgathe B Nkoy, Floreen M Mumaka, Ange Ngonde, et al.
Pageof 8