खोज परिणाम - Mathijs Willemsen

  • प्रदर्शित 1 - 5 परिणाम 5
परिणाम को परिष्कृत करें
  1. 1
    Monogenic Adult-Onset Inborn Errors of Immunity

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

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
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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 द्वारा 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

    प्रकाशित 2020
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    Revisão
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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 द्वारा 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

    प्रकाशित 2021
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    Artigo
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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 द्वारा 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

    प्रकाशित 2020
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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 द्वारा 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

    प्रकाशित 2020
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