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Frederik Staels

Showing results (11-20 of 30) with videos related to

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Rheumatology Advances in Practice|April 4, 2022
Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiencyMathijs Willemsen, Erika Van Nieuwenhove, Nasim Sadat Seyed Tabib, et al.
Journal of Clinical Immunology|May 8, 2023
CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 DeficiencyMargaux Gerbaux, Evelyne Roos, Mathijs Willemsen, et al.
Clinical Immunology (Orlando, Fla.)|March 1, 2026
Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial diseaseWillem Roosens, Marjon Wouters, Frederik Staels, et al.
Frontiers in Immunology|October 5, 2023
Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature studyWillem Roosens, Frederik Staels, Sien Van Loo, et al.
Frontiers in Immunology|November 2, 2020
Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the LiteratureFrederik Staels, Albrecht Betrains, Peter Doubel, et al.
Journal of Clinical Immunology|July 13, 2022
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial DiseaseFrederik Staels, Flaminia Lorenzetti, Kerstin De Keukeleere, et al.
Frontiers in Immunology|April 6, 2023
Case report: Myocarditis in congenital STAT1 gain-of functionFrederik Staels, Willem Roosens, Simone Giovannozzi, et al.
Frontiers in Immunology|May 28, 2021
Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation SyndromeFrederik Staels, Albrecht Betrains, F J Sherida H Woei-A-Jin, et al.
Science Immunology|July 24, 2021
Unstable regulatory T cells, enriched for naïve and Nrp1<sup>neg</sup> cells, are purged after fate challengeSteffie Junius, Adamantios V Mavrogiannis, Pierre Lemaitre, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2019
Mutations in <i>MAGT1</i> lead to a glycosylation disorder with a variable phenotypeEline Blommaert, Romain Péanne, Natalia A Cherepanova, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Rheumatology Advances in Practice|April 4, 2022
Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiencyMathijs Willemsen, Erika Van Nieuwenhove, Nasim Sadat Seyed Tabib, et al.
Journal of Clinical Immunology|May 8, 2023
CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 DeficiencyMargaux Gerbaux, Evelyne Roos, Mathijs Willemsen, et al.
Clinical Immunology (Orlando, Fla.)|March 1, 2026
Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial diseaseWillem Roosens, Marjon Wouters, Frederik Staels, et al.
Frontiers in Immunology|October 5, 2023
Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature studyWillem Roosens, Frederik Staels, Sien Van Loo, et al.
Frontiers in Immunology|November 2, 2020
Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the LiteratureFrederik Staels, Albrecht Betrains, Peter Doubel, et al.
Journal of Clinical Immunology|July 13, 2022
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial DiseaseFrederik Staels, Flaminia Lorenzetti, Kerstin De Keukeleere, et al.
Frontiers in Immunology|April 6, 2023
Case report: Myocarditis in congenital STAT1 gain-of functionFrederik Staels, Willem Roosens, Simone Giovannozzi, et al.
Frontiers in Immunology|May 28, 2021
Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation SyndromeFrederik Staels, Albrecht Betrains, F J Sherida H Woei-A-Jin, et al.
Science Immunology|July 24, 2021
Unstable regulatory T cells, enriched for naïve and Nrp1<sup>neg</sup> cells, are purged after fate challengeSteffie Junius, Adamantios V Mavrogiannis, Pierre Lemaitre, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2019
Mutations in <i>MAGT1</i> lead to a glycosylation disorder with a variable phenotypeEline Blommaert, Romain Péanne, Natalia A Cherepanova, et al.
Pageof 3