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

per Willemsen, Mathijs, Schouten, Harry C.
Publicat a Biomark Res (2017)

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

per Willemsen, Mathijs, Abdul Hamid, Myrurgia, Winkens, Bjorn, zur Hausen, Axel
Publicat a Blood Cancer J (2018)

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

per Ruijters, Erik J. B., Haenen, Guido R. M. M., Willemsen, Mathijs, Weseler, Antje R., Bast, Aalt
Publicat a 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

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

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

per 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
Publicat a Front Immunol (2020)

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

per 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
Publicat a Front Immunol (2021)

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

per 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
Publicat a Clin Transl Immunology (2020)

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

per 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
Publicat a J Allergy Clin Immunol (2020)