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Clinical Immunology, ISSN 1521-6616, 2015, Volume 166-167, pp. 19 - 26
Abstract Common Variable Immunodeficiency (CVID) is a primary immunodeficiency characterized by B cell dysfunction and decreased serum immunoglobulin. CVID... 
Allergy and Immunology | T helper cells | Activation | Common variable immunodeficiency | Memory B cells | Co-stimulation | Cytokine | ABNORMALITIES | RECEPTOR | IMMUNOLOGY | DEFICIENCY | IMMUNE DYSREGULATION | HYPOGAMMAGLOBULINEMIA | DISEASE | MUTATIONS | ICOS | EXPRESSION | LYMPHOCYTES | Common Variable Immunodeficiency - immunology | Cell Proliferation | Humans | Middle Aged | Interleukin-17 - immunology | Interleukin-13 - immunology | Male | Interleukin-13 - genetics | Inducible T-Cell Co-Stimulator Protein - genetics | Adult | Female | B-Lymphocytes - pathology | T-Lymphocytes - pathology | B-Cell Activation Factor Receptor - genetics | Inducible T-Cell Co-Stimulator Protein - immunology | B-Cell Activation Factor Receptor - immunology | Severity of Illness Index | Cross-Sectional Studies | Signal Transduction | Lymphocyte Activation | Common Variable Immunodeficiency - pathology | Gene Expression Regulation | Interleukin-17 - genetics | CTLA-4 Antigen - genetics | Common Variable Immunodeficiency - genetics | CTLA-4 Antigen - immunology | B7-H1 Antigen - genetics | B7-H1 Antigen - immunology | B-Lymphocytes - immunology | Interleukin-9 - genetics | Interleukin-10 - genetics | Lymphocyte Count | Immunologic Memory | T-Lymphocytes - immunology | Aged | Primary Cell Culture | Programmed Cell Death 1 Receptor - immunology | Interleukin-10 - immunology | Interleukin-9 - immunology | Programmed Cell Death 1 Receptor - genetics | Index Medicus
Journal Article
Journal of the European Academy of Dermatology and Venereology : JEADV, 08/2019
Autoinflammation and phospholipase Cγ2-associated antibody deficiency and immune dysregulation (APLAID) is an exceedingly rare monogenic autoinflammatory... 
Index Medicus
Journal Article
Revista de Investigacion Clinica, ISSN 0034-8376, 04/2014, Volume 66, Issue 2, pp. 164 - 172
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 2/2014, Volume 34, Issue 2, pp. 146 - 156
Journal Article
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion, ISSN 0034-8376, 03/2014, Volume 66, Issue 2, pp. 164 - 172
Journal Article
Revista Alergia México, ISSN 0002-5151, 02/2017, Volume 64, Issue 1, p. 87
Journal Article
Case reports in immunology, ISSN 2090-6609, 2019, Volume 2019, p. 6357256
Hyper-IgE syndrome (HIES) is a rare primary immunodeficiency characterized by elevated levels of immunoglobulin E (IgE), eczematous dermatitis, cold abscesses,... 
Journal Article
Revista Alergia México, ISSN 0002-5151, 02/2017, Volume 64, Issue 1, pp. 87 - 108
Common variable immunodeficiency (IDCV) is the largest group of symptomatic primary immune deficiencies; it is characterized by hypogammaglobulinemia, poor... 
Células T | Inmunodeficiencia común variable | Células B | Respuesta innata
Journal Article
Revista Alergia Mexico, ISSN 0002-5151, 01/2017, Volume 64, Issue 1, pp. 87 - 108
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2012, Volume 32, Issue 5, pp. 967 - 974
Journal Article
Immunologic Research, ISSN 0257-277X, 3/2015, Volume 61, Issue 3, pp. 260 - 268
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, 02/2012, Volume 5, p. S46
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, 02/2012, Volume 5, p. S191
Journal Article
Revista Alergia México, ISSN 0002-5151, 07/2018, Volume 65, Issue 2, p. 171
Journal Article
Revista Alergia Mexico, ISSN 0002-5151, 04/2018, Volume 65, Issue 2, pp. 171 - 177
Journal Article
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