Risultati della ricerca - Veerle Labarque

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

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Barriers to and Facilitators of Pediatric Palliative Care in Mainland China, Hong Kong, and Taiwan: A Document Analysis di Yajing Zhong, Chris Gastmans, Veerle Labarque, Alice Cavolo

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A multiplex allele-specific polymerase chain reaction assay for rapid and affordable detection of APOL1 risk variants di Oyindamola Christiana Adebayo, Inge Bongaers, Elena Levtchenko, Lambertus van den Heuvel, Veerle Labarque

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APOL1-mediated kidney disease: a narrative review of the lessons learnt from the past 15 years di Oyindamola Christiana Adebayo, Henry Chijindu Okpoli, Joris Vriens, Elena Levtchenko, Lambertus van den Heuvel, Veerle Labarque

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

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

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OUTCOME OF SECOND HEMATOPOIETIC STEM CELL TRANSPLANTATION IN PEDIATRIC PATIENTS WITH SEVERE APLASTIC ANEMIA di Nienke Wieringa, Michael Amrein, Michael Dworzak, Jan Stary, Owen Smith, Veerle Labarque, Franco Locatelli, Jochen Büchner, Katarzyna Pawelec, Markus Schmugge, Marc Bierings, Brigitte Strahm

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Clinical utility of panel-based genetic sequencing for von Willebrand disease di 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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COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet di 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

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