Resultados da pesquisa - Mathijs Willemsen

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  1. 1
    Monogenic Adult-Onset Inborn Errors of Immunity

    Monogenic Adult-Onset Inborn Errors of Immunity Por Frederik Staels, Tom Collignon, Albrecht Betrains, Margaux Gerbaux, Mathijs Willemsen, Stéphanie Humblet‐Baron, Adrian Liston, Steven Vanderschueren, Rik Schrijvers

    Publicado em 2021
    Obter o texto integral Obter o texto integral
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  2. 2
    Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature

    Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature Por Frederik Staels, Albrecht Betrains, Peter Doubel, Mathijs Willemsen, Vincent Cleemput, Steven Vanderschueren, Anniek Corveleyn, Isabelle Meyts, Ben Sprangers, Yanick J. Crow, Stéphanie Humblet‐Baron, Adrian Liston, Rik Schrijvers

    Publicado em 2020
    Obter o texto integral Obter o texto integral
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  3. 3
    Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome

    Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome Por Frederik Staels, Albrecht Betrains, F. J. Sherida H. Woei‐A‐Jin, Nancy Boeckx, M. Beckers, An Bervoets, Mathijs Willemsen, Barbara Neerinckx, Stéphanie Humblet‐Baron, Daniël Blockmans, Steven Vanderschueren, Rik Schrijvers

    Publicado em 2021
    Obter o texto integral Obter o texto integral
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  4. 4
    Increased IL‐10‐producing regulatory T cells are characteristic of severe cases of COVID‐19

    Increased IL‐10‐producing regulatory T cells are characteristic of severe cases of COVID‐19 Por Julika Neumann, Teresa Prezzemolo, Lore Vanderbeke, Carlos P. Roca, Margaux Gerbaux, Silke Janssens, Mathijs Willemsen, Oliver T. Burton, Pierre Van Mol, Yannick Van Herck, Joost Wauters, Els Wauters, Adrian Liston, Stéphanie Humblet‐Baron

    Publicado em 2020
    Obter o texto integral Obter o texto integral
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  5. 5
    Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia

    Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia Por Erika Van Nieuwenhove, John S. Barber, Julika Neumann, Elien Smeets, Mathijs Willemsen, Emanuela Pasciuto, Teresa Prezzemolo, Vasiliki Lagou, Laura Seldeslachts, Bert Malengier‐Devlies, Mieke Metzemaekers, Sarah Haßdenteufel, Axelle Kerstens, Rob van der Kant, Frédéric Rousseau, Joost Schymkowitz, Daniele Di Marino, Sven Lang, Richard Zimmermann, Susan Schlenner, Sebastian Munck, Paul Proost, Patrick Matthys, Christine Devalck, Nancy Boeckx, Frank Claessens, Carine Wouters, Stéphanie Humblet‐Baron, Isabelle Meyts, Adrian Liston

    Publicado em 2020
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