Inappropriate costimulation and aberrant DNA methylation as therapeutic targets in angioimmunoblastic T-cell lymphoma

由 Willemsen, Mathijs, Schouten, Harry C.
發表在 Biomark Res (2017)

Mutational heterogeneity of angioimmunoblastic T-cell lymphoma indicates distinct lymphomagenic pathways

由 Willemsen, Mathijs, Abdul Hamid, Myrurgia, Winkens, Bjorn, zur Hausen, Axel
發表在 Blood Cancer J (2018)

Food-Derived Bioactives Can Protect the Anti-Inflammatory Activity of Cortisol with Antioxidant-Dependent and -Independent Mechanisms

由 Ruijters, Erik J. B., Haenen, Guido R. M. M., Willemsen, Mathijs, Weseler, Antje R., Bast, Aalt
發表在 Int J Mol Sci (2016)

A Rare Case of Angioimmunoblastic T-Cell Lymphoma with Epstein-Barr Virus-Negative Reed-Sternberg-Like B-Cells, Chylous Ascites, and Chylothorax

由 Willemsen, Mathijs, Dielis, Arne W. J. H., Samarska, Iryna V., Koster, Ad, van Marion, Arienne M.
發表在 Case Rep Hematol (2017)

Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature

由 Staels, Frederik, Betrains, Albrecht, Doubel, Peter, Willemsen, Mathijs, Cleemput, Vincent, Vanderschueren, Steven, Corveleyn, Anniek, Meyts, Isabelle, Sprangers, Ben, Crow, Yanick J., Humblet-Baron, Stephanie, Liston, Adrian, Schrijvers, Rik
發表在 Front Immunol (2020)

Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome

由 Staels, Frederik, Betrains, Albrecht, Woei-A-Jin, F. J. Sherida H., Boeckx, Nancy, Beckers, Marielle, Bervoets, An, Willemsen, Mathijs, Neerinckx, Barbara, Humblet-Baron, Stephanie, Blockmans, Daniel Engelbert, Vanderschueren, Steven, Schrijvers, Rik
發表在 Front Immunol (2021)

Increased IL‐10‐producing regulatory T cells are characteristic of severe cases of COVID‐19

由 Neumann, Julika, Prezzemolo, Teresa, Vanderbeke, Lore, Roca, Carlos P, Gerbaux, Margaux, Janssens, Silke, Willemsen, Mathijs, Burton, Oliver, Van Mol, Pierre, Van Herck, Yannick, Wauters, Joost, Wauters, Els, Liston, Adrian, Humblet‐Baron, Stephanie
發表在 Clin Transl Immunology (2020)

Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia

由 Van Nieuwenhove, Erika, Barber, John S., Neumann, Julika, Smeets, Elien, Willemsen, Mathijs, Pasciuto, Emanuela, Prezzemolo, Teresa, Lagou, Vasiliki, Seldeslachts, Laura, Malengier-Devlies, Bert, Metzemaekers, Mieke, Haßdenteufel, Sarah, Kerstens, Axelle, van der Kant, Rob, Rousseau, Frederic, Schymkowitz, Joost, Di Marino, Daniele, Lang, Sven, Zimmermann, Richard, Schlenner, Susan, Munck, Sebastian, Proost, Paul, Matthys, Patrick, Devalck, Christine, Boeckx, Nancy, Claessens, Frank, Wouters, Carine, Humblet-Baron, Stephanie, Meyts, Isabelle, Liston, Adrian
發表在 J Allergy Clin Immunol (2020)