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Clinical Immunology, ISSN 1521-6616, 2011, Volume 141, Issue 1, pp. 90 - 102
Journal Article
British Journal of Haematology, ISSN 0007-1048, 11/2011, Volume 155, Issue 4, pp. 498 - 508
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 10/2013, Volume 123, Issue 10, pp. 4283 - 4293
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, p. e74893
About half of all subjects with common variable immune deficiency (CVID) are afflicted with inflammatory complications including hematologic autoimmunity,... 
MEMORY B-CELLS | IMMUNODEFICIENCY DISORDERS | TRANSCRIPTIONAL SIGNATURE | MULTIDISCIPLINARY SCIENCES | PATTERNS | ALPHA | ANTIBODY-DEFICIENCY | PERIPHERAL-BLOOD | PATIENT | MUTATIONS | EXPRESSION | Humans | Middle Aged | Molecular Sequence Annotation | Gene Expression Regulation | Transcriptome | Common Variable Immunodeficiency - genetics | Male | Gene Expression Profiling | Common Variable Immunodeficiency - blood | Common Variable Immunodeficiency - complications | Inflammation - etiology | Case-Control Studies | Inflammation - blood | Young Adult | Interferons - blood | Interferon-alpha - blood | Adolescent | Aged, 80 and over | Adult | Female | Aged | Child | Interferon-gamma - blood | Cluster Analysis | Autoimmunity | Lung diseases | Mortality | Genes | Disease susceptibility | Interferon | B cells | Biological response modifiers | Comparative analysis | Health aspects | Health care | Transcription | Pathogenesis | Gene regulation | Hyperplasia | Arthritis | Infections | Activation | Males | Immunity | Blood | Inflammatory diseases | Proteins | Immunology | Pathways | Age | Immune system | Lupus | Antigens | Immunoglobulins | Bacterial infections | Complications | Adaptive immunity | Gene expression | Patients | Morbidity | Medicine | Studies | Lymphocytes B | Lymphopenia | Biopsy | Biomarkers | Mutation | Environmental monitoring | Autoimmune diseases
Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 09/2012, Volume 169, Issue 3, pp. 263 - 272
Summary Common variable immunodeficiency disorders (CVID), the most frequent cause of symptomatic primary immunodeficiency, are defined by impaired antibody... 
CVID | monocyte activation | common variable immunodeficiency | plasma LPS | T cell activation | Common variable immunodeficiency | Monocyte activation | Plasma LPS | X-LINKED AGAMMAGLOBULINEMIA | IMMUNE-DEFICIENCY | PERIPHERAL-BLOOD | IMMUNOLOGY | DENDRITIC CELL-FUNCTION | HIV-INFECTION | MICROBIAL TRANSLOCATION | UP-REGULATION | PD-1 | T-CELLS | DISEASE PROGRESSION | T-Lymphocyte Subsets - immunology | Common Variable Immunodeficiency - immunology | Agammaglobulinemia - immunology | Immunoglobulin G - blood | Humans | Middle Aged | Male | Monocytes - immunology | Common Variable Immunodeficiency - blood | Protein-Tyrosine Kinases - deficiency | Lipopolysaccharides - blood | Immunoglobulin G - immunology | Adult | Female | Antibodies, Bacterial - blood | Carrier Proteins - blood | Receptors, IgG - blood | Acute-Phase Proteins | Lymphocyte Activation | Membrane Glycoproteins - blood | Lipopolysaccharide Receptors - blood | Monocytes - chemistry | Agammaglobulinemia - blood | T-Lymphocyte Subsets - pathology | Endotoxins - immunology | Antibodies, Bacterial - immunology | GPI-Linked Proteins - blood | Cytokines - biosynthesis | Fc receptors | Genetic disorders | Immunoglobulin G | Immunological deficiency syndromes | T cells | Mitogens | Emergency medical services | Plasma | T cell receptors | Lymphocytes | Immune system | Original
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 08/2005, Volume 202, Issue 4, pp. 479 - 484
Journal Article