Immunological abnormalities associated with hereditary haemorrhagic telangiectasia - Guilhem, A.; Malcus, C.; Clarivet, B.; Plauchu, H.; Dupuis‐Girod, S. (Journal of internal medicine, 2013)
Keywords: Abnormalities; Adaptive immunity; Adult; Aged; Aged, 80 and over; CD4 antigen; CD4-Positive T-Lymphocytes - immunology; CD8 antigen; CD8-Positive T-Lymphocytes - immunology; Cell proliferation; Chemotaxis; Endoglin; Female; Genetic disorders; Growth factors; Health risks; hereditary hemorrhagic telangiectasia; Humans; Hypergammaglobulinemia - etiology; Hypergammaglobulinemia - immunology; Immunity; Immunity, Innate - genetics; Immunoglobulin A - immunology; Immunoglobulin G - immunology; Immunoglobulin M; Immunoglobulins; immunoglobulins M; immunologic deficiency syndromes; Immunology; Infections; Innate immunity; Iron; Lymphocytes; Lymphocytes T; Lymphopenia; Lymphopenia - etiology; Lymphopenia - immunology; Male; Middle Aged; Monocytes; Mutation; Natural killer cells; Phagocytosis; Primary immunodeficiencies; Prospective Studies; Risk analysis; Risk Factors; Signs and symptoms; Subpopulations; Supplements; T lymphocytopenia; Telangiectasia, Hereditary Hemorrhagic - complications; Telangiectasia, Hereditary Hemorrhagic - genetics; Telangiectasia, Hereditary Hemorrhagic - immunology; Transforming growth factor; Transforming growth factor-b; Young Adult; T lymphocytopenia; immunologic deficiency syndromes; immunoglobulins M; hereditary hemorrhagic telangiectasia