All papers authored by Mathijs Willemsen
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2023
Mathijs Willemsen 
,
John S. Barber,
Erika Van Nieuwenhove,
Frederik Staels,
Margaux Gerbaux ,
Julika Neumann,
Teresa Prezzemolo,
Emanuela Pasciuto ,
Vasiliki Lagou,
Nancy Boeckx,
Jessica Filtjens,
Amber De Visscher,
Patrick Matthys,
Rik Schrijvers,
Thomas Tousseyn
and 6 other authors
,
John S. Barber,
Erika Van Nieuwenhove,
Frederik Staels,
Margaux Gerbaux ,
Julika Neumann,
Teresa Prezzemolo,
Emanuela Pasciuto ,
Vasiliki Lagou,
Nancy Boeckx,
Jessica Filtjens,
Amber De Visscher,
Patrick Matthys,
Rik Schrijvers,
Thomas Tousseyn
and 6 other authors
Homozygous DBF4 mutation as a cause of severe congenital neutropenia
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2022
Frederik Staels,
Kerstin De Keukeleere,
Matias Kinnunen,
Salla Keskitalo,
Flaminia Lorenzetti,
Michiel Vanmeert,
Teresa Prezzemolo,
Emanuela Pasciuto ,
Eveline Lescrinier,
Xavier Bossuyt,
Margaux Gerbaux ,
Mathijs Willemsen ,
Julika Neumann,
Sien Van Loo,
Anniek Corveleyn
and 8 other authors
Download from doi.org
,
Eveline Lescrinier,
Xavier Bossuyt,
Margaux Gerbaux ,
Mathijs Willemsen ,
Julika Neumann,
Sien Van Loo,
Anniek Corveleyn
and 8 other authors
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Frederik Staels,
Flaminia Lorenzetti,
Kerstin De Keukeleere,
Mathijs Willemsen ,
Margaux Gerbaux ,
Julika Neumann,
Thomas Tousseyn,
Emanuela Pasciuto ,
Paul De Munter,
Xavier Bossuyt,
Rik Gijsbers,
Adrian Liston,
Stephanie Humblet-Baron,
Rik Schrijvers
,
Margaux Gerbaux ,
Julika Neumann,
Thomas Tousseyn,
Emanuela Pasciuto ,
Paul De Munter,
Xavier Bossuyt,
Rik Gijsbers,
Adrian Liston,
Stephanie Humblet-Baron,
Rik Schrijvers
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease
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Elien Smeets ,
Shengyun Huang,
Xiao Yin Lee,
Erika Van Nieuwenhove,
Christine Helsen,
Florian Handle ,
Lisa Moris,
Sarah El Kharraz,
Roy Eerlings,
Wout Devlies ,
Mathijs Willemsen ,
Leoni Bücken,
Teresa Prezzemolo,
Stephanie Humblet‐Baron,
Arnout Voet
and 4 other authors
Download from doi.org
,
Shengyun Huang,
Xiao Yin Lee,
Erika Van Nieuwenhove,
Christine Helsen,
Florian Handle ,
Lisa Moris,
Sarah El Kharraz,
Roy Eerlings,
Wout Devlies ,
Mathijs Willemsen ,
Leoni Bücken,
Teresa Prezzemolo,
Stephanie Humblet‐Baron,
Arnout Voet
and 4 other authors
Download from doi.org
2021
Frederik Staels,
Tom Collignon,
Albrecht Betrains,
Margaux Gerbaux ,
Mathijs Willemsen ,
Stephanie Humblet-Baron,
Adrian Liston,
Steven Vanderschueren,
Rik Schrijvers
,
Mathijs Willemsen ,
Stephanie Humblet-Baron,
Adrian Liston,
Steven Vanderschueren,
Rik Schrijvers
Monogenic Adult-Onset Inborn Errors of Immunity
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Frederik Staels,
F. J. Sherida H. Woei-A.-Jin,
Albrecht Betrains,
S. Woei-A.-Jin,
Sherida Woei A. Jin,
Nancy Boeckx,
Marielle Beckers,
An Bervoets,
Mathijs Willemsen ,
Barbara Neerinckx,
Stephanie Humblet-Baron,
Daniel Engelbert Blockmans,
Steven Vanderschueren,
Rik Schrijvers
,
Barbara Neerinckx,
Stephanie Humblet-Baron,
Daniel Engelbert Blockmans,
Steven Vanderschueren,
Rik Schrijvers
Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome
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2020
Julika Neumann,
Jonas Yserbyt,
Teresa Prezzemolo,
Lore Vanderbeke,
Carlos P. Roca,
Margaux Gerbaux ,
Silke Janssens,
Mathijs Willemsen ,
Roca Cp,
Oliver Burton,
Pierre Van Mol,
Yannick Van Herck,
Francesca Bosisio,
Joost Wauters,
Frederik De Smet
and 24 other authors
,
Silke Janssens,
Mathijs Willemsen ,
Roca Cp,
Oliver Burton,
Pierre Van Mol,
Yannick Van Herck,
Francesca Bosisio,
Joost Wauters,
Frederik De Smet
and 24 other authors
Increased IL-10-producing regulatory T cells are characteristic of severe cases of COVID-19.
Download from onlinelibrary.wiley.com
Frederik Staels,
Albrecht Betrains,
Peter Doubel,
Mathijs Willemsen ,
Vincent Cleemput,
Steven Vanderschueren,
Anniek Corveleyn,
Isabelle Meyts,
Ben Sprangers,
Yanick J. Crow,
Stephanie Humblet-Baron,
Adrian Liston,
Rik Schrijvers
Download from doi.org
,
Vincent Cleemput,
Steven Vanderschueren,
Anniek Corveleyn,
Isabelle Meyts,
Ben Sprangers,
Yanick J. Crow,
Stephanie Humblet-Baron,
Adrian Liston,
Rik Schrijvers
Download from doi.org
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,
Frederic Rousseau
and 15 other authors
,
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,
Frederic Rousseau
and 15 other authors
Defective SEC61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
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