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N‐methyl‐D‐aspartate receptor antibody production from germinal center reactions: Therapeutic implications

Annals of neurology, 2018-03, Vol.83 (3), p.553-561

2018

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The clinical features, underlying immunology, and treatment of autoantibody‐mediated movement disorders

Movement disorders, 2018-09, Vol.33 (9), p.1376-1389

2018

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Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects

Journal of allergy and clinical immunology, 2013-02, Vol.131 (2), p.477-485.e1

2013

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B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans

Proceedings of the National Academy of Sciences - PNAS, 2009-08, Vol.106 (33), p.13945-13950

2009

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The EuroFlow PID Orientation Tube for Flow Cytometric Diagnostic Screening of Primary Immunodeficiencies of the Lymphoid System

Frontiers in immunology, 2019-03, Vol.10, p.246-246

2019

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Genetic CD21 deficiency is associated with hypogammaglobulinemia

Journal of allergy and clinical immunology, 2012-03, Vol.129 (3), p.801-810.e6

2012

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EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System

Frontiers in immunology, 2019-06, Vol.10, p.1271-1271

2019

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Inhibition of human B-cell development into plasmablasts by histone deacetylase inhibitor valproic acid

Journal of allergy and clinical immunology, 2013-06, Vol.131 (6), p.1695-1699.e9

2013

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Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools

Frontiers in immunology, 2021-02, Vol.11, p.603972-603972

2021

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Key stages of bone marrow B-cell maturation are defective in patients with common variable immunodeficiency disorders

Journal of allergy and clinical immunology, 2015-08, Vol.136 (2), p.487-490.e2

2015

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Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE

Clinical immunology (Orlando, Fla.), 2016-02, Vol.163, p.17-21

2016

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Condition-dependent generation of aquaporin-4 antibodies from circulating B cells in neuromyelitis optica

Brain (London, England : 1878), 2018-04, Vol.141 (4), p.1063-1074

2018

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High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation

PloS one, 2014-06, Vol.9 (6), p.e100328-e100328

2014

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Cervical lymph nodes and ovarian teratomas as germinal centres in NMDA receptor-antibody encephalitis

Brain (London, England : 1878), 2022-08, Vol.145 (8), p.2742-2754

2022

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Rituximab abrogates aquaporin-4-specific germinal center activity in patients with neuromyelitis optica spectrum disorders

Proceedings of the National Academy of Sciences - PNAS, 2022-06, Vol.119 (24), p.e2121804119-e2121804119

2022

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Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

Clinical immunology (Orlando, Fla.), 2015-10, Vol.160 (2), p.301-314

2015

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Variable phenotype and discrete alterations of immune phenotypes in CTP synthase 1 deficiency: Report of 2 siblings

Journal of allergy and clinical immunology, 2016-12, Vol.138 (6), p.1722-1725.e6

2016

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B cell Biology: An Overview

Current allergy and asthma reports, 2014-05, Vol.14 (5), p.434-434, Article 434

2014

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38.3 ONGOING GERMINAL CENTRE REACTIONS CONTRIBUTE TO N-METHYL-D-ASPARTATE RECEPTOR (NMDAR) ANTIBODY PRODUCTION IN NMDAR-ANTIBODY ENCEPHALITIS

Schizophrenia bulletin, 2018-04, Vol.44 (suppl_1), p.S61-S61

2018

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Human B Cell Development and Tolerance

Encyclopedia of Immunobiology, 2016, p.105-121

2016

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Human CARD11 deficiency causes profound combined immunodeficiency (P3325)

The Journal of immunology (1950), 2013-05, Vol.190 (1_Supplement), p.175-175.10

2013

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Deficiency of caspase recruitment domain family, memberANB11 (CARD11), causes profound combined immunodeficiency in human subjects

Journal of allergy and clinical immunology, 2013-02, Vol.131 (2), p.477-485.e1

2013

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F.112. Human BAFF-R Deficiency is Associated with Primary Antibody Deficiency Syndrome

Clinical immunology (Orlando, Fla.), 2009, Vol.131, p.S123-S123

2009

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OR.4. Common Variable Immunodeficiency (CVID) Correlates with B Cell-specific Class-switch Recombination Defects

Clinical immunology (Orlando, Fla.), 2008, Vol.127, p.S5-S5

2008

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N‐methyl‐D‐aspartate receptor antibody production from germinal center reactions: Therapeutic implications

The clinical features, underlying immunology, and treatment of autoantibody‐mediated movement disorders

Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans

The EuroFlow PID Orientation Tube for Flow Cytometric Diagnostic Screening of Primary Immunodeficiencies of the Lymphoid System

Genetic CD21 deficiency is associated with hypogammaglobulinemia

EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System

Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis

Inhibition of human B-cell development into plasmablasts by histone deacetylase inhibitor valproic acid

Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools

Key stages of bone marrow B-cell maturation are defective in patients with common variable immunodeficiency disorders

Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE

Condition-dependent generation of aquaporin-4 antibodies from circulating B cells in neuromyelitis optica

High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation

Cervical lymph nodes and ovarian teratomas as germinal centres in NMDA receptor-antibody encephalitis

Rituximab abrogates aquaporin-4-specific germinal center activity in patients with neuromyelitis optica spectrum disorders

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

Variable phenotype and discrete alterations of immune phenotypes in CTP synthase 1 deficiency: Report of 2 siblings

B cell Biology: An Overview

38.3 ONGOING GERMINAL CENTRE REACTIONS CONTRIBUTE TO N-METHYL-D-ASPARTATE RECEPTOR (NMDAR) ANTIBODY PRODUCTION IN NMDAR-ANTIBODY ENCEPHALITIS

Human B Cell Development and Tolerance

Human CARD11 deficiency causes profound combined immunodeficiency (P3325)

Deficiency of caspase recruitment domain family, memberANB11 (CARD11), causes profound combined immunodeficiency in human subjects

F.112. Human BAFF-R Deficiency is Associated with Primary Antibody Deficiency Syndrome

OR.4. Common Variable Immunodeficiency (CVID) Correlates with B Cell-specific Class-switch Recombination Defects

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