Definition of Iron Deficiency Based on the Gold Standard of Bone Marrow Iron Staining in Heart Failure Patients von Grote Beverborg, Niels, Klip, IJsbrand T, Meijers, Wouter C, Voors, Adriaan A, Vegter, Eline L, van der Wal, Haye H, Swinkels, Dorine W, van Pelt, Joost, Mulder, Andre B, Bulstra, Sjoerd K, Vellenga, Edo, Mariani, Massimo A, de Boer, Rudolf A, van Veldhuisen, Dirk J, van der Meer, Peter

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Newest Fetal Cell Count™ Kit for the detection of fetomaternal hemorrhage shows good clinical performance von Meijer, Kees, Boorsma, Carian, Mulder, André B., Scharnhorst, Volkher

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β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study von Croles, Frederik Nanne, Mulder, René, Mulder, André B., Lukens, Michaël V., Meijer, Karina

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In Normal Controls, Both Age and Gender Affect Coagulability as Measured by Thrombelastography von Roeloffzen, Wilfried W. H., Kluin-Nelemans, Hanneke C., Mulder, Andre B., Veeger, Nic J. G. M., Bosman, Lotte, de Wolf, Joost Th M.

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Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency von Mulder, René, Wiewel-Verschueren, Sophie, Meijer, Karina, Mulder, André B.

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The IL1-IL1RAP axis plays an important role in the inflammatory leukemic niche that favors acute myeloid leukemia proliferation over normal hematopoiesis von De Boer, Bauke, Sheveleva, Sofia, Apelt, Katja, Vellenga, Edo, Mulder, Andre B., Huls, Gerwin, Schuringa, Jan Jacob

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SERPINC1 gene mutations in antithrombin deficiency von Mulder, René, Croles, F. Nanne, Mulder, André B., Huntington, James A., Meijer, Karina, Lukens, Michaël V.

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Sinusoidal endothelial cells are damaged and display enhanced autophagy in myelodysplastic syndromes von Houwerzijl, Ewout J., Heuvel, Fiona A. J., Blom, Nel R., Want, Johannes J. L., Mulder, André B., Vellenga, Edo

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Prospective Isolation and Characterization of Genetically and Functionally Distinct AML Subclones von de Boer, Bauke, Prick, Janine, Pruis, Maurien G., Keane, Peter, Imperato, Maria Rosaria, Jaques, Jennifer, Brouwers-Vos, Annet Z., Hogeling, Shanna M., Woolthuis, Carolien M., Nijk, Marije T., Diepstra, Arjan, Wandinger, Sebastian, Versele, Matthias, Attar, Ricardo M., Cockerill, Peter N., Huls, Gerwin, Vellenga, Edo, Mulder, André B., Bonifer, Constanze, Schuringa, Jan Jacob

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Inhibition of autophagy as a treatment strategy for p53 wild-type acute myeloid leukemia von Folkerts, Hendrik, Hilgendorf, Susan, Wierenga, Albertus T J, Jaques, Jennifer, Mulder, André B, Coffer, Paul J, Schuringa, Jan Jacob, Vellenga, Edo

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Measuring apoptosis in human spermatozoa: a biological assay for semen quality? von Oosterhuis, G.Jurjen E, Mulder, Andre B, Kalsbeek-Batenburg, Ellen, Lambalk, Cornelis B, Schoemaker, Joop, Vermes, Istvan

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Monitoring of heparins in antithrombin-deficient patients von Croles, Frederik Nanne, Lukens, Michaël V., Mulder, René, de Maat, Moniek P.M., Mulder, André B., Meijer, Karina

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Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin (F2) gene mutation in a Dutch Caucasian family with unexplained thrombosis von Mulder, Rene, Lisman, Ton, Meijers, Joost C. M., Huntington, James A., Mulder, Andre B., Meijer, Karina

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Hereditary Alpha Tryptasemia: Validation of a Single-Well Multiplex Digital Droplet PCR Assay in a Cohort of Symptomatic Patients von Alheraky, Abdulrazzaq, Wierenga, Albertus T J, Simpelaar, Arjan, Hesp, Lucy B, Minovic, Isidor, Bagheri, Niusha, Roozendaal, Caroline, Span, Lambert F R, Oude Elberink, Hanneke N G, Kema, Ido P, Mulder, André B

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Midostaurin in patients with indolent systemic mastocytosis: An open-label phase 2 trial von van Anrooij, Bjorn, Oude Elberink, Joanne N.G., Span, Lambert F.R., de Monchy, Jan G.R., Rosati, Stefano, Mulder, André B., Kluin-Nelemans, Johanna C.

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Targeted RNA-Sequencing Enables Detection of Relevant Translocations and Single Nucleotide Variants and Provides a Method for Classification of Hematological Malignancies-RANKING von de Lange, Kim, de Boer, Eddy N., Bosga, Anneke, Alimohamed, Mohamed Z., Johansson, Lennart F., Mulder, Andre B., Vellenga, Edo, van Diemen, Cleo C., Deelen, Patrick, van den Berg, Eva, Sikkema-Raddatz, Birgit

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Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis von Wouters, Hanneke J.C.M., Mulder, René, van Zeventer, Isabelle A., Schuringa, Jan Jacob, van der Klauw, Melanie M., van der Harst, Pim, Diepstra, Arjan, Mulder, André B., Huls, Gerwin

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Anti‐IFC antibodies in a patient with CHAPLE syndrome: Implications for blood management von Minović, Isidor, Schipperus, Martin R., Mäkelburg, Anja B. U., Meijer, Kornelis, Lukens, Michaël V., Kootstra‐Ros, Jenny E., Heide, Frans, Abbasova, Ilhama, Kleine, Ruben H. J., Meekers, Johan H., Mulder, André B.

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Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co‐occurring FANCC and CHEK2 mutations von Berger, Gerbrig, Berg, Eva, Smetsers, Stephanie, Leegte, Beike K., Sijmons, Rolf H., Abbott, Kristin M., Mulder, André B., Vellenga, Edo

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Non‐small‐cell lung cancer infiltrated with chronic myelomonocytic leukaemia: a molecular diagnostic challenge to recognise mixed cancers in a single biopsy von Koopman, Bart, Hiddinga, Birgitta I, Platteel, Inge, Kluiver, Joost L, Timens, Wim, Mulder, André B, Doesum, Jaap A, Schuuring, Ed, Diepstra, Arjan, Kempen, Léon C

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