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

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Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature study von Roosens, Willem, Staels, Frederik, Van Loo, Sien, Humblet-Baron, Stephanie, Meyts, Isabelle, De Samblanx, Hadewijch, Verslype, Chris, van Malenstein, Hannah, van der Merwe, Schalk, Laleman, Wim, Schrijvers, Rik

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Case report: Myocarditis in congenital STAT1 gain-of function von Staels, Frederik, Roosens, Willem, Giovannozzi, Simone, Moens, Leen, Bogaert, Jan, Iglesias-Herrero, Cecilia, Gijsbers, Rik, Bossuyt, Xavier, Frans, Glynis, Liston, Adrian, Humblet-Baron, Stephanie, Meyts, Isabelle, Van Aelst, Lucas, Schrijvers, Rik

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Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations von Staels, Frederik, De Keukeleere, Kerstin, Kinnunen, Matias, Keskitalo, Salla, Lorenzetti, Flaminia, Vanmeert, Michiel, Prezzemolo, Teresa, Pasciuto, Emanuela, Lescrinier, Eveline, Bossuyt, Xavier, Gerbaux, Margaux, Willemsen, Mathijs, Neumann, Julika, Van Loo, Sien, Corveleyn, Anniek, Willekens, Karen, Stalmans, Ingeborg, Meyts, Isabelle, Liston, Adrian, Humblet-Baron, Stephanie, Seppänen, Mikko, Varjosalo, Markku, Schrijvers, Rik

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A double-edged sword von Vandebotermet, Martijn, Staels, Frederik, Giovannozzi, Simone, Delforge, Michel, Tousseyn, Thomas, Steelandt, Thomas, Corveleyn, Anniek, Meyts, Isabelle, Maertens, Johan, Yserbyt, Jonas, Schrijvers, Rik

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Metformin as add‐on to intensive insulin therapy in type 1 diabetes mellitus von Staels, Frederik, Moyson, Carolien, Mathieu, Chantal

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Systemic autoinflammatory disease in adults von Betrains, Albrecht, Staels, Frederik, Schrijvers, Rik, Meyts, Isabelle, Humblet-Baron, Stephanie, De Langhe, Ellen, Wouters, Carine, Blockmans, Daniel, Vanderschueren, Steven

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DNA replication-associated inborn errors of immunity von Willemsen, Mathijs, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Schrijvers, Rik, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency von Gerbaux, Margaux, Roos, Evelyne, Willemsen, Mathijs, Staels, Frederik, Neumann, Julika, Bücken, Leoni, Haughton, Jeason, Yshii, Lidia, Dooley, James, Schlenner, Susan, Humblet-Baron, Stephanie, Liston, Adrian

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Homozygous DBF4 mutation as a cause of severe congenital neutropenia von Willemsen, Mathijs, Barber, John S., Nieuwenhove, Erika Van, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Prezzemolo, Teresa, Pasciuto, Emanuela, Lagou, Vasiliki, Boeckx, Nancy, Filtjens, Jessica, De Visscher, Amber, Matthys, Patrick, Schrijvers, Rik, Tousseyn, Thomas, O’Driscoll, Mark, Bucciol, Giorgia, Schlenner, Susan, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature study von Roosens, Willem, Staels, Frederik, Van Loo, Sien, Humblet-Baron, Stephanie, Meyts, Isabelle, De Samblanx, Hadewijch, Verslype, Chris, van Malenstein, Hannah, van der Merwe, Schalk, Laleman, Wim, Schrijvers, Rik

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Inflammatory aortitis in a patient with type 2 hyper IgM syndrome von Staels, Frederik, Betrains, Albrecht, Willemsen, Mathijs, Corvelyn, Anniek, Tousseyn, Thomas, Dierickx, Daan, Humblet-Baron, Stephanie, Liston, Adrian, Vanderschueren, Steven, Schrijvers, Rik

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Homozygous DBF4 mutation as a cause of severe congenital neutropenia von Willemsen, Mathijs, Barber, John S, Van Nieuwenhove, Erika, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Prezzemolo, Teresa, Pasciuto, Emanuela, Lagou, Vasiliki, Boeckx, Nancy, Filtjens, Jessica, De Visscher, Amber, Matthys, Patrick, Schrijvers, Rik, Tousseyn, Thomas, O'Driscoll, Mark, Bucciol, Giorgia, Schlenner, Susan, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease von Staels, Frederik, Lorenzetti, Flaminia, De Keukeleere, Kerstin, Willemsen, Mathijs, Gerbaux, Margaux, Neumann, Julika, Tousseyn, Thomas, Pasciuto, Emanuela, De Munter, Paul, Bossuyt, Xavier, Gijsbers, Rik, Liston, Adrian, Humblet-Baron, Stephanie, Schrijvers, Rik

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Diagnosis of deficiency of adenosine deaminase type 2 in adulthood von Betrains, Albrecht, Staels, Frederik, Moens, Leen, Delafontaine, Selket, Hershfield, Michael, Blockmans, Daniel, Liston, Adrian, Humblet-Baron, Stephanie, Meyts, Isabelle, Schrijvers, Rik, Vanderschueren, Steven

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Case report: Myocarditis in congenital STAT1 gain-of function von Staels, Frederik, Roosens, Willem, Giovannozzi, Simone, Moens, Leen, Bogaert, Jan, Iglesias-Herrero, Cecilia, Gijsbers, Rik, Bossuyt, Xavier, Frans, Glynis, Liston, Adrian, Humblet-Baron, Stephanie, Meyts, Isabelle, Van Aelst, Lucas, Schrijvers, Rik

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OTULIN haploinsufficiency predisposes to environmentally directed inflammation von Staels, Frederik, Bucken, Leoni, De Vuyst, Leana, Willemsen, Mathijs, Van Nieuwenhove, Erika, Gerbaux, Margaux, Neumann, Julika, Malviya, Vanshika, Van Meerbeeck, Lize, Haughton, Jeason, Seldeslachts, Laura, Gouwy, Mieke, Martinod, Kimberly, Vande Velde, Greetje, Proost, Paul, Yshii, Lidia, Schlenner, Susan, Schrijvers, Rik, Liston, Adrian, Humblet-Baron, Stephanie

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Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome von Staels, Frederik, Betrains, Albrecht, Woei-A-Jin, Sherida, Boeckx, Nancy, Beckers, Marielle, Bervoets, An, Willemsen, Mathijs, Neerinckx, Barbara, Humblet-Baron, Stephanie, Blockmans, Daniel Engelbert, Vanderschueren, Steven, Schrijvers, Rik

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Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects von Neumann, Julika, Van Nieuwenhove, Erika, Terry, Lara E, Staels, Frederik, Knebel, Taylor R, Welkenhuyzen, Kirsten, Ahmadzadeh, Kourosh, Baker, Mariah R, Gerbaux, Margaux, Willemsen, Mathijs, Barber, John S, Serysheva, Irina I, De Waele, Liesbeth, Vermeulen, Francois, Schlenner, Susan, Meyts, Isabelle, Yule, David, Bultynck, Geert, Schrijvers, Rik, Humblet-Baron, Stephanie, Liston, Adrian

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Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations von Staels, Frederik, De Keukeleere, Kerstin, Kinnunen, Matias, Keskitalo, Salla, Lorenzetti, Flaminia, Vanmeert, Michiel, Prezzemolo, Teresa, Pasciuto, Emanuela, Lescrinier, Eveline, Bossuyt, Xavier, Gerbaux, Margaux, Willemsen, Mathijs, Neumann, Julika, Van Loo, Sien, Corveleyn, Anniek, Willekens, Karen, Stalmans, Ingeborg, Meyts, Isabelle, Liston, Adrian, Humblet-Baron, Stephanie, Seppanen, Mikko, Varjosalo, Markku, Schrijvers, Rik

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