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Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 134, Issue 1, pp. 116 - 126.e11
Background Common variable immunodeficiency (CVID) is an antibody deficiency with an equal sex distribution and a high variability in clinical presentation.... 
Allergy and Immunology | patient self-reported outcomes | treatment | Common variable immunodeficiency | primary antibody deficiency | autoimmunity | enteropathy | immunoglobulin replacement | quality of life | lymphadenopathy | granulomas | INFECTIONS | PHENOTYPES | IMMUNOLOGY | DEFICIENCY | IGM | TRIAL | B-CELL | ALLERGY | HYPOGAMMAGLOBULINEMIA | INTRAVENOUS IMMUNOGLOBULIN | DISEASE | Autoimmunity | Common Variable Immunodeficiency - immunology | Common Variable Immunodeficiency - drug therapy | Humans | Child, Preschool | Lymphoproliferative Disorders - complications | Male | Lymphoproliferative Disorders - immunology | Splenomegaly - pathology | Bronchiectasis - pathology | Common Variable Immunodeficiency - mortality | Pneumonia - mortality | Pneumonia - immunology | Adult | Female | Retrospective Studies | Child | Europe | Delayed Diagnosis | Common Variable Immunodeficiency - complications | Lymphoproliferative Disorders - mortality | Pneumonia - drug therapy | Immunoglobulins, Intravenous - therapeutic use | Adolescent | Age of Onset | Survival Analysis | Pneumonia - complications | Lymphoproliferative Disorders - drug therapy | Immunological deficiency syndromes | Care and treatment | Health aspects | Respiratory tract diseases | Studies | Pneumonia | Meningitis | Lymphomas | Multivariate analysis | Patients | Age | Data bases
Journal Article
Haematologica, ISSN 0390-6078, 07/2015, Volume 100, Issue 7, pp. 978 - 988
Hemophagocytic lymphohistiocytosis is a hyperinflammatory syndrome defined by clinical and laboratory criteria. Current criteria were created to identify... 
DEFECTS | CHRONIC GRANULOMATOUS-DISEASE | MACROPHAGE ACTIVATION SYNDROME | BONE-MARROW | PERFORIN | HEMATOLOGY | CYTOTOXICITY | DEFICIENCY | TRANSPLANTATION | MANIFESTATIONS | DELETION | Lymphohistiocytosis, Hemophagocytic - pathology | Humans | Child, Preschool | Lymphoproliferative Disorders - complications | Male | Virus Diseases - complications | Virus Diseases - drug therapy | T-Lymphocytes - drug effects | Opportunistic Infections - immunology | Immunologic Deficiency Syndromes - immunology | Child | Infant, Newborn | Lymphohistiocytosis, Hemophagocytic - immunology | Opportunistic Infections - complications | Leishmaniasis - immunology | Virus Diseases - immunology | Bacterial Infections - drug therapy | Lymphohistiocytosis, Hemophagocytic - drug therapy | Europe | Lymphohistiocytosis, Hemophagocytic - diagnosis | Terminology as Topic | Leishmaniasis - drug therapy | Immunoglobulins, Intravenous - therapeutic use | Adolescent | Mycoses - drug therapy | T-Lymphocytes - immunology | Immunologic Deficiency Syndromes - drug therapy | Killer Cells, Natural - drug effects | Mycoses - complications | Mycoses - immunology | Infant | Killer Cells, Natural - pathology | Lymphoproliferative Disorders - immunology | Bacterial Infections - complications | Bacterial Infections - immunology | Killer Cells, Natural - immunology | Adult | Female | Registries | Steroids - therapeutic use | T-Lymphocytes - pathology | Immunologic Deficiency Syndromes - diagnosis | Diagnosis, Differential | Immunologic Deficiency Syndromes - complications | Lymphoproliferative Disorders - diagnosis | Opportunistic Infections - drug therapy | Lymphoproliferative Disorders - drug therapy | Leishmaniasis - complications | Immunologic Factors - therapeutic use
Journal Article
American Journal of Transplantation, ISSN 1600-6135, 02/2013, Volume 13, Issue s3, pp. 41 - 54
Journal Article
Cancer Letters, ISSN 0304-3835, 2011, Volume 305, Issue 2, pp. 163 - 174
Journal Article
Blood, ISSN 0006-4971, 10/2013, Volume 122, Issue 18, pp. 3101 - 3110
Journal Article
European Journal of Haematology, ISSN 0902-4441, 07/2013, Volume 91, Issue 1, pp. 20 - 28
Journal Article
Journal Article
American Journal of Kidney Diseases, ISSN 0272-6386, 2015, Volume 66, Issue 5, pp. 756 - 767
Background Kidney diseases associated with immunoglobulin M (IgM) monoclonal gammopathy are poorly described, with few data for patient outcomes and renal... 
Nephrology | tubular disorder | membranoproliferative glomerulonephritis | amyloidosis | kidney biopsy | cast nephropathy | Monoclonal gammopathy | renal response | Waldenström magroglobulinemia | Fanconi syndrome | B-cell lymphoproliferative disorder | IgM | MULTIPLE-MYELOMA | IMMUNOLOGICAL FEATURES | WALDENSTROMS MACROGLOBULINEMIA | RENAL SIGNIFICANCE | DEPOSITION DISEASE | Waldenstrom magroglobulinemia | HEAVY-CHAIN | INTERNATIONAL WORKSHOP | LIGHT-CHAIN AMYLOIDOSIS | UNDETERMINED SIGNIFICANCE | UROLOGY & NEPHROLOGY | NEPHROTIC SYNDROME | Lymphoma, B-Cell - complications | Humans | Middle Aged | Kidney Neoplasms - immunology | Lymphoproliferative Disorders - complications | Male | Lymphoproliferative Disorders - immunology | Immunoglobulin M - immunology | Waldenstrom Macroglobulinemia - pathology | Nephritis, Interstitial - pathology | Paraproteinemias - pathology | Waldenstrom Macroglobulinemia - complications | Amyloidosis - immunology | Lymphoma, B-Cell - immunology | Aged, 80 and over | Adult | Female | Amyloidosis - etiology | Retrospective Studies | Acute Kidney Injury - immunology | Kidney Neoplasms - complications | Acute Kidney Injury - etiology | Antibodies, Monoclonal - immunology | Paraproteinemias - immunology | Glomerulonephritis, Membranoproliferative - pathology | Amyloidosis - pathology | Acute Kidney Injury - pathology | Kidney Diseases - pathology | Nephrotic Syndrome - pathology | Paraproteinemias - complications | Kidney Diseases - immunology | Nephrotic Syndrome - immunology | Waldenstrom Macroglobulinemia - immunology | Glomerulonephritis, Membranoproliferative - immunology | B-Lymphocytes - immunology | Lymphoma, B-Cell - pathology | Amyloid - immunology | Nephritis, Interstitial - etiology | Kidney Neoplasms - pathology | Aged | Kidney Diseases - etiology | Glomerulonephritis, Membranoproliferative - etiology | Nephritis, Interstitial - immunology | Nephrotic Syndrome - etiology | Cohort Studies | Life Sciences | Immunology
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2011, Volume 127, Issue 6, pp. 1329 - 1341.e2
Primary immunodeficiencies (PIDs) are commonly characterized by an increased susceptibility to specific infections and, in certain instances, a higher than... 
Allergy and Immunology |