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Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2010, Volume 125, Issue 6, pp. 1354 - 1360.e4
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2012, Volume 129, Issue 5, pp. 1425 - 1426.e3
Journal Article
Journal Article
Journal Article
Clinical and Experimental Immunology, ISSN 1365-2249, 2017, Volume 190, Issue 2, pp. 226 - 234
Many patients with primary immunodeficiency (PID) who have antibody deficiency develop progressive lung disease due to underlying subclinical infection and... 
primary immunodeficiency disease | antibody deficiency | subclinical infection | lung disease | monitoring | BACTERIA | BRONCHIECTASIS | COMMON VARIABLE IMMUNODEFICIENCY | IMMUNE-DEFICIENCY | IMMUNOLOGY | CHILDREN | PRIMARY HYPOGAMMAGLOBULINEMIA | LUNG-DISEASE | VIRUSES | Spirometry | Asymptomatic Infections - epidemiology | Humans | Male | Adult | Female | Retrospective Studies | Immunologic Deficiency Syndromes - immunology | Child | Immunologic Deficiency Syndromes - therapy | Immunologic Deficiency Syndromes - complications | Lung Diseases - diagnosis | Europe | Lung Diseases - prevention & control | Medical Records | Immunoglobulin G - therapeutic use | Ambulatory Care | Agammaglobulinemia - physiopathology | Lung Diseases - immunology | Immunologic Deficiency Syndromes - physiopathology | Common Variable Immunodeficiency - physiopathology | Immunization, Passive | Respiratory System - physiopathology | Lung Diseases - complications | Immunoglobulins - therapeutic use | Practice Guidelines as Topic | Surveys | Medical research | Immunoglobulin G | Lung diseases | Medicine, Experimental | Medical records | Pulmonary function tests | Chest | Respiratory function | Common variable immunodeficiency | Subclinical infection | Microbiology | Laboratories | Complications | Antibodies | Infections | Patients | Laboratory tests | Sinus | Adults | Children | Health risk assessment | Monitoring | Original | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Lungmedicin och allergi | Klinisk medicin | Respiratory Medicine and Allergy
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 9/2010, Volume 30, Issue 5, pp. 734 - 745
Subcutaneous human IgG (SCIG) therapy in primary immunodeficiency (PID) offers sustained IgG levels throughout the dosing cycle and fewer adverse events (AEs)... 
serum IgG trough levels | Medical Microbiology | Biomedicine | Immunology | home infusion therapy | L-proline | Subcutaneous immunoglobulin (SCIG) | primary immunodeficiency | Internal Medicine | Infectious Diseases | local tolerability | PRIMARY ANTIBODY DEFICIENCIES | HUMAN INTRAVENOUS IMMUNOGLOBULIN | IGG | COMMON VARIABLE IMMUNODEFICIENCY | INFUSION | IMMUNOLOGY | REPLACEMENT THERAPY | QUALITY-OF-LIFE | HOME THERAPY | 10-PERCENT | IGIV-C | Common Variable Immunodeficiency - immunology | Agammaglobulinemia - immunology | Prospective Studies | Common Variable Immunodeficiency - drug therapy | Immunoglobulin G - blood | Humans | Middle Aged | Male | Common Variable Immunodeficiency - blood | Agammaglobulinemia - drug therapy | Genetic Diseases, X-Linked - drug therapy | Injections, Subcutaneous | Adult | Female | Protein Stability | Child | Genetic Diseases, X-Linked - physiopathology | Genetic Diseases, X-Linked - blood | Immunologic Factors - administration & dosage | Agammaglobulinemia - physiopathology | Genetic Diseases, X-Linked - immunology | Bacterial Infections - prevention & control | Agammaglobulinemia - blood | Immunoglobulins, Intravenous - therapeutic use | Adolescent | Common Variable Immunodeficiency - physiopathology | Aged | Immunologic Factors - adverse effects | Immunologic Factors - therapeutic use | Complications and side effects | Allergy | Bacterial infections | Immunoglobulin G | Immunodeficiency | Proline | Universities and colleges | Allergic reaction
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 8/2017, Volume 37, Issue 6, pp. 592 - 602
Common variable immunodeficiency (CVID) is a complex, heterogeneous immunodeficiency characterized by hypogammaglobulinemia, recurrent infections, and poor... 
Medical Microbiology | CVID | infection | fatigue | Biomedicine | Immunology | Common variable immunodeficiency | autoimmunity | inflammation | Infectious Diseases | Internal Medicine | USIDNET | PHENOTYPES | PREVALENCE | IMMUNOLOGY | CHILDREN | DISEASE | HEALTH | CELL | IMMUNODEFICIENCY | BLOOD | Autoimmunity | United States - epidemiology | Arthritis - physiopathology | Depression - physiopathology | Arthritis - epidemiology | Bronchitis - epidemiology | Humans | Middle Aged | Child, Preschool | Male | Otitis Media - physiopathology | Young Adult | Common Variable Immunodeficiency - epidemiology | Aged, 80 and over | Adult | Female | Retrospective Studies | Child | Failure to Thrive - physiopathology | Databases, Factual | Developmental Disabilities - physiopathology | Depression - epidemiology | Bronchitis - physiopathology | Developmental Disabilities - epidemiology | Phenotype | Cell Transformation, Neoplastic | Adolescent | Age of Onset | Failure to Thrive - epidemiology | Common Variable Immunodeficiency - physiopathology | Aged | Otitis Media - epidemiology | Longitudinal Studies | Pediatrics | Medical research | Analysis | Immunoglobulin G | Medicine, Experimental | Respiratory tract diseases | Fatigue | Adults | Immunoglobulin A | Health aspects | Immunoglobulin M | Vaccination | Prophylaxis | Arthritis | Hypogammaglobulinemia | Malignancy | Antibody response | Bronchitis | Children | Age | Immunoglobulins | Statistical analysis | Lung diseases | Lymphoma | Computer programs | Antibiotics | Otitis media | Autoimmune diseases | Health risk assessment
Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 07/2011, Volume 165, Issue 1, pp. 1 - 7
Journal Article