Onderzoeker
Veerle Mondelaers
- Disciplines:Endocrinologie en metabole ziekten, Pediatrie en neonatologie, Verpleegkunde
Affiliaties
- Vakgroep Inwendige ziekten en Pediatrie (Departement)
Lid
Vanaf1 okt 2018 → Heden - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf19 sep 2016 → 30 sep 2018
Publicaties
1 - 10 of 15 results
- Prospective, real-time monitoring of pegylated Escherichia coli and Erwinia asparaginase therapy in childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma in Belgium(2020)
Auteurs: Veerle Mondelaers, Alina Ferster, Anne Uyttebroeck, Benedicte Brichard, Juttevan der Werff ten Bosch, Koenraad Norga, Nadine Francotte, Caroline Piette, Katrien Vandemeulebroecke, Charlotte Verbeke, et al.
Pagina's: 105 - 114 - A novel L-asparaginase with low L-glutaminase coactivity is highly efficacious against both T- and B-cell acute lymphoblastic leukemias in vivo(2018)
Auteurs: Hien Anh Nguyen, Ying Su, Jenny Yu Zhang, Aleksandar Antanasijevic, Michael Caffrey, Amanda M Schalk, Li Liu, Damiano Rondelli, Annie Oh, Dolores L Mahmud, et al.
Pagina's: 1549 - 1560 - Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia(2017)
Auteurs: Alessandro Casini, R Vilar, Y Beauverd, D Aslan, Katrien Devreese, Veerle Mondelaers, L Alberio, C Gubert, P de Moerloose, Marguerite Neerman-Arbez
Pagina's: 583 - 589 - Prolonged versus standard native E-coli asparaginase therapy in childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma : final results of the EORTC-CLG randomized phase III trial 58951(2017)
Auteurs: Veerle Mondelaers, Stefan Suciu, Barbara De Moerloose, Alina Ferster, Francoise Mazingue, Geneviève Plat, Karima Yakouben, Anne Uyttebroeck, Patrick Lutz, Vitor Costa, et al.
Pagina's: 1727 - 1738 - Leukemia in infants : a retrospective study (1992-2014) in the Ghent University Hospital(2016)Volume: 18
Auteurs: Elise Nauwynck, Tim Lammens, Vincent Vakaet, N Van Damme, Yves Benoit, Veerle Mondelaers, Els Vandecruys, Genevieve Laureys, L Vakaet, Barbara De Moerloose
Aantal pagina's: 1 - Report of five novel fibrinogen mutations leading to congenital hypofibrinogenemia(2016)
Auteurs: A Casini, J Lotta, D Aslan, Katrien Devreese, E De Maistre, P De Moerloose, Veerle Mondelaers, M Neerman-Arbez
Aantal pagina's: 1 - Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations(2014)
Auteurs: É Katona, L Muszbek, Katrien Devreese, KB Kovács, Z Bereczky, M Jonkers, AH Shemirani, Veerle Mondelaers, AAM Ermens
Pagina's: 114 - 120 - Acute lymphoblastic leukemia in children with Down syndrome: a retrospective analysis from the Ponte di Legno study group(2014)
Auteurs: Trudy D Buitenkamp, Shai Izraeli, Martin Zimmermann, Erik Forestier, Nyla A Heerema, Marry M van den Heuvel-Eibrink, Rob Pieters, Carin M Korbijn, Lewis B Silverman, Kjeld Schmiegelow, et al.
Pagina's: 70 - 77 - Screening for hereditary spherocytosis in routine practice : evaluation of a diagnostic algorithm with focus on non-splenectomised patients(2012)
Auteurs: Lies Persijn, Carolien Bonroy, Veerle Mondelaers, ANNA VANTILBORGH, Jan Philippé, Veronique Stove
Pagina's: 301 - 302 - Musculoskeletal manifestations in children with acute lymphoblastic leukaemia(2012)
Auteurs: HILDE MULDER, Nele Herregods, Veerle Mondelaers, Yves Benoit, VALERIE MEERSSCHAUT, Barbara De Moerloose
Pagina's: 3 - 11