Search Results - Veerle Labarque

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  1. 1

    Hemostatic phenotypes and genetic disorders by Fabienne Ver Donck, Veerle Labarque, Kathleen Freson

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  2. 2

    Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence by Yajing Zhong, Alice Cavolo, Veerle Labarque, Chris Gastmans

    Published in BMC Palliative Care (2022-06-01)
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  3. 3

    Physicians’ attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence by Yajing Zhong, Alice Cavolo, Veerle Labarque, Chris Gastmans

    Published in BMC Palliative Care (2023-09-01)
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  4. 4

    Chinese and Belgian pediatricians’ perspectives toward pediatric palliative care: an online survey by Yajing Zhong, Alice Cavolo, Veerle Labarque, Bernadette Dierckx de Casterlé, Chris Gastmans

    Published in BMC Palliative Care (2024-04-01)
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  5. 5

    Long-Term Outcome of Single-Session, Ultrasound-Guided, Radiofrequency Ablation for Symptomatic Small, Lower Limb, Venous Malformations by Laurence Verhaeghe, Veerle Labarque, Jan Vranckx, Inge Fourneau, Steven Pans, Geert Maleux

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  6. 6

    Case report: Cardiac intimal sarcoma in a young child by Sanne Verbeek, Raf Sciot, Maria Debiec-Rychter, Veerle Labarque, Bart Meyns, Bjorn Cools

    Published in Frontiers in Pediatrics (2023-09-01)
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  7. 7

    Transcriptome profiling of megakaryocytes and platelets: Application to GP9‐ and IKZF5‐related thrombocytopenia by Koenraad De Wispelaere, Fabienne Ver Donck, Kato Ramaekers, Chantal Thys, Koji Eto, Veerle Labarque, Ernest Turro, Kathleen Freson

    Published in HemaSphere (2025-09-01)
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  8. 8

    Factor VIII genotype and the risk of developing high-responding or low-responding inhibitors in severe hemophilia A: data from the PedNet Hemophilia Cohort of 1,202 children by Nadine G. Andersson, Veerle Labarque, Mutlu Kartal-Kaess, Fernando Pinto, Torben Stamm Mikkelsen, Rolf Ljung, PedNet Study Group

    Published in Haematologica (2023-10-01)
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  9. 9

    Methylene tetrahydrofolate reductase A1298C polymorphisms influence the adult sequelae of chemotherapy in childhood-leukemia survivors. by Iris Elens, Sabine Deprez, Thibo Billiet, Charlotte Sleurs, Veerle Labarque, Anne Uyttebroeck, Stefaan Van Gool, Jurgen Lemiere, Rudi D'Hooge

    Published in PLoS ONE (2021-01-01)
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  10. 10

    Clinical utility of panel-based genetic sequencing for von Willebrand disease by Radha Ramanan, Christine Van Laer, Sarissa Baert, Cyrielle Kint, Chris Van Geet, Quentin Van Thillo, Peter Verhamme, Thomas Vanassche, James D. McFadyen, Andrew C. Perkins, Huyen A. Tran, Veerle Labarque, Kathleen Freson

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  11. 11

    Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia by Tadbir K. Bariana, Veerle Labarque, Jessica Heremans, Chantal Thys, Mara De Reys, Daniel Greene, Benjamin Jenkins, Luigi Grassi, Denis Seyres, Frances Burden, Deborah Whitehorn, Olga Shamardina, Sofia Papadia, Keith Gomez, NIHR BioResource, Chris Van Geet, Albert Koulman, Willem H. Ouwehand, Cedric Ghevaert, Mattia Frontini, Ernest Turro, Kathleen Freson

    Published in Haematologica (2019-05-01)
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  12. 12

    LIN28B is over-expressed in specific subtypes of pediatric leukemia and regulates lncRNA H19 by Hetty H. Helsmoortel, Barbara De Moerloose, Tim Pieters, Farzaneh Ghazavi, Silvia Bresolin, Hélène Cavé, Andrica de Vries, Valerie de Haas, Christian Flotho, Veerle Labarque, Charlotte Niemeyer, Pascale De Paepe, Nadine Van Roy, Jan Stary, Marry M. van den Heuvel-Eibrink, Yves Benoit, Johannes Schulte, Steven Goossens, Geert Berx, Jody J. Haigh, Frank Speleman, Pieter Van Vlierberghe, Tim Lammens

    Published in Haematologica (2016-06-01)
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  13. 13

    COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet by Pablo Velasco Puyo, Soteroula Christou, Saveria Campisi, Maria A. Rodríguez-Sánchez, Sara Reidel, Santiago Perez-Hoyo, Miriam Mota, Irene Savvidou, Anna Rekleiti, Alessandra Salvo, Vincenzo Voi, Giovanni Battista Ferrero, Giorgia Mandrile, Carmen Maria Gaglioti, Elena Cela, Beatriz Ponce-Salas, Eduardo J. Bardón-Cancho, Pagona Flevari, Ersi Voskaridou-Dimoula, Erfan Nur, Bart J. Biemond, Polynexi Delaporta, David Beneitez-Pastor, Anna Collado Gimbert, Anna Spasiano, Tatiana Besse-Hammer, Ioannis G. Lafiatis, Laurence Dedeken, Simona Raso, Anna Ruiz-Llobet, Sabrina Bagnato, Veerle Labarque, Andreas Glenthøj, Giovan Battista Ruffo, Maria Elena Guerzoni, Kaoutar Hafraoui, Laura Pistoia, Rosamaria Rosso, Laura Tagliaferri, Paula Gonzalez-Urdiales, Fleur Samantha Benghiat, Mariane de Montalembert, Maria Jose Teles, Anna Vanderfaeillie, Elisa Bertoni, Daniela Cuzzubbo, Teresa Ferreira, Christopher J. Saunders, Eftichia Stiakaki, Ann L. Van de Velde, Michael D. Diamantidis, Jean-Louis H. Kerkhoffs, Marisa I. Oliveira, Alessandra Quota, Roberta Russo, An Van Damme, María Argüello Marina, Mikael Lorite Reggiori, Anita W. Rijneveld, Alexis Rodríguez Gallego, Raffaella Colombatti, Achille Iolascon, Ali Taher, Béatrice Gulbis, Noémi B. A. Roy, María del Mar Mañú-Pereira

    Published in Orphanet Journal of Rare Diseases (2025-04-01)
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