D. Bogaert

发表

A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects

C. Bonroy, S. Rosenzweig, E. De Baere, 2017, The Journal of allergy and clinical immunology.

A CARD9 Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation

B. Lambrecht, J. Casanova, S. Savvides, 2018, Front. Immunol..

Familial Mediterranean fever mutations lift the obligatory requirement for microtubules in Pyrin inflammasome activation

E. De Baere, M. Lamkanfi, D. Bogaert, 2016, Proceedings of the National Academy of Sciences.

Case Report: Convalescent Plasma, a Targeted Therapy for Patients with CVID and Severe COVID-19

B. Lambrecht, A. Sette, P. Maes, 2020, Frontiers in Immunology.

A Computational Pipeline for the Diagnosis of CVID Patients

Y. Saeys, S. Van Gassen, S. Tavernier, 2019, Front. Immunol..

Congenital Defects of Phagocytes

D. Bogaert, F. Haerynck, 2021, Cellular Primary Immunodeficiencies.

Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

B. Lambrecht, S. Rosenzweig, E. De Baere, 2017, Scientific Reports.

Raised immunoglobulin A and circulating T follicular helper cells are linked to the development of food allergy in paediatric liver transplant patients

B. Lambrecht, P. Gevaert, F. Gottrand, 2015, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50

J. Walter, J. Church, M. Varjosalo, 2022, Frontiers in Immunology.

Calcineurin inhibitors dampen humoral immunity by acting directly on naive B cells

B. Lambrecht, P. Gevaert, D. Bogaert, 2015, Clinical and experimental immunology.

GTF3A mutations predispose to herpes simplex encephalitis by disrupting biogenesis of the host-derived RIG-I ligand RNA5SP141

B. Lambrecht, P. de Bleser, E. De Baere, 2022, Science Immunology.

How to recognize inborn errors of immunity in a child presenting with a malignancy: guidelines for the pediatric hemato-oncologist

U. Fischer, D. Bogaert, R. Wagener, 2022, Pediatric hematology and oncology.

GATA2 deficiency and haematopoietic stem cell transplantation: challenges for the clinical practitioner

B. Lambrecht, A. Hsu, S. Tavernier, 2019, British journal of haematology.

Erratum to: Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency

B. Lambrecht, J. Casanova, J. Lambert, 2016, Journal of Clinical Immunology.

Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency

B. Lambrecht, J. Casanova, J. Lambert, 2016, Journal of Clinical Immunology.

Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency

B. Lambrecht, J. Casanova, J. Lambert, 2016, Journal of Clinical Immunology.

Severe phototoxicity associated with concomitant use of methotrexate and voriconazole, an overlooked drug‐drug interaction

D. Bogaert, E. Verhaeghe, G. Laureys, 2020, Pediatric blood & cancer.

Genes associated with common variable immunodeficiency: one diagnosis to rule them all?

B. Lambrecht, D. Bogaert, F. Haerynck, 2016, Journal of Medical Genetics.

Ikaros family zinc finger 1 regulates dendritic cell development and function in humans

A. Gennery, S. Rosenzweig, K. Voelkerding, 2018, Nature Communications.

Persistent rotavirus diarrhea post‐transplant in a novel JAK3‐SCID patient after vaccination

C. Bonroy, D. Bogaert, F. Haerynck, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Familial hemophagocytic lymphohistiocytosis type 3 presenting as neonatal cholestasis and splenomegaly

D. Bogaert, A. Vanlander, F. Haerynck, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive TH17 immunity.

C. Bonroy, K. Venken, E. van de Vijver, 2018, The Journal of allergy and clinical immunology.

The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives

B. Lambrecht, C. Bonroy, J. Philippé, 2017, Haematologica.

Molecular genetics of common variable immunodeficiency

E. Baere, D. Bogaert, F. Haerynck, 2017 .

A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

Y. Saeys, B. Lambrecht, P. Verloo, 2019, Nature Communications.

Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

B. Lambrecht, S. Rosenzweig, H. Kuehn, 2017, Scientific Reports.

Editorial: The role of transcription factors in inborn errors of immunity

H. Kuehn, D. Bogaert, F. Haerynck, 2023, Frontiers in Immunology.

Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

Y. Saeys, B. Lambrecht, P. Verloo, 2019, Nature Communications.

Raised immunoglobulin A and circulating T follicular helper cells are linked to the development of food allergy in paediatric liver transplant patients

P. Gevaert, D. Bogaert, M. Dullaers, 2015, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive TH17 immunity.

C. Bonroy, K. Venken, E. van de Vijver, 2018, The Journal of allergy and clinical immunology.