Monogenic Adult-Onset Inborn Errors of Immunity

por Staels, Frederik, Collignon, Tom, Betrains, Albrecht, Gerbaux, Margaux, Willemsen, Mathijs, Humblet-Baron, Stephanie, Liston, Adrian, Vanderschueren, Steven, Schrijvers, Rik
Publicado 2021

A double-edged sword

por Vandebotermet, Martijn, Staels, Frederik, Giovannozzi, Simone, Delforge, Michel, Tousseyn, Thomas, Steelandt, Thomas, Corveleyn, Anniek, Meyts, Isabelle, Maertens, Johan, Yserbyt, Jonas, Schrijvers, Rik
Publicado 2020

Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency

por Willemsen, Mathijs, Van Nieuwenhove, Erika, Seyed Tabib, Nasim Sadat, Staels, Frederik, Schrijvers, Rik, De Somer, Lien, Liston, Adrian, Humblet-Baron, Stephanie, Wouters, Carine
Publicado 2022

CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency

por 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
Publicado 2023

Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature study

por 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
Publicado 2023

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

por 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
Publicado 2020

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

por 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
Publicado 2021

Case report: Myocarditis in congenital STAT1 gain-of function

por 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
Publicado 2023

A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease

por 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
Publicado 2022

Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations

por 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
Publicado 2022

Author Correction: Disrupted Ca(2+) homeostasis and immunodeficiency in patients with functional IP(3) receptor subtype 3 defects

por 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, François, Schlenner, Susan, Meyts, Isabelle, Yule, David I., Bultynck, Geert, Schrijvers, Rik, Humblet-Baron, Stephanie, Liston, Adrian
Publicado 2022

Disrupted Ca(2+) homeostasis and immunodeficiency in patients with functional IP(3) receptor subtype 3 defects

por 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, François, Schlenner, Susan, Meyts, Isabelle, Yule, David I., Bultynck, Geert, Schrijvers, Rik, Humblet-Baron, Stephanie, Liston, Adrian
Publicado 2022