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Current Allergy and Asthma Reports, ISSN 1529-7322, 3/2019, Volume 19, Issue 3, pp. 1 - 1
The section heading that reads PI3K100δ Deficiency should be corrected to read PI3K110δ Deficiency. 
Allergology | Medicine & Public Health | Medical colleges | Killer cells | Immunodeficiency
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 06/2018, Volume 141, Issue 6, pp. 2142 - 2155.e5
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2018, Volume 38, Issue 7, pp. 753 - 756
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s10875-018-0554-3 
Hematopoietic stem cell transplant | STAT1 gain of function | Common variable immunodeficiency | Chronic mucocutaneous candidiasis | Combined immunodeficiency | UNDERLIE | IMMUNOLOGY | Mycoses | Medical colleges | Genetic aspects | Transplantation | Diagnosis | Hematopoietic stem cells | Stat1 protein | Immunodeficiency
Journal Article
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 Clinical Immunology, ISSN 0271-9142, 2/2014, Volume 34, Issue 2, pp. 146 - 156
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2017, Volume 12, Issue 8, pp. e0181134 - e0181134
Journal Article
IUBMB Life, ISSN 1521-6543, 04/2012, Volume 64, Issue 4, pp. 346 - 353
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 137, Issue 2, pp. AB217 - AB217
  Immune evaluation demonstrated absent IgA, normal IgG and IgM, poor specific antibody responses after vaccination, mild CD4+ T cell lymphopenia with an... 
Allergy and Immunology | Viral antibodies | Mycoses | Antibodies | Health aspects | Flow cytometry | Growth hormones | Mutation | Fungal infections
Journal Article
Blood, ISSN 0006-4971, 01/2015, Volume 125, Issue 4, pp. 591 - 599
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2012, Volume 32, Issue 5, pp. 967 - 974
Journal Article
FRONTIERS IN PEDIATRICS, ISSN 2296-2360, 04/2019, Volume 7, p. 160
In this report, we describe a novel T437N STAT1 mutation found in a mother and 3 of her 4 children which we demonstrate yields gain-of-function. All of the... 
STAT1 | gain-of-function | UNDERLIE | primary immunodeficiency | PEDIATRICS | human immunology | Hodgkin lymphoma | Lymphadenopathy | Lymphomas | Genetic aspects
Journal Article
FRONTIERS IN PEDIATRICS, ISSN 2296-2360, 04/2019, Volume 7, p. 130
Autosomal dominant hyper-IgE syndrome caused by mutations in the transcription factor STAT3 (AD-HIES) is characterized by a collection of immunologic and... 
AD-HIES | pneumonia | STAT3 | Job syndrome | eczema | case report | PEDIATRICS | Immunoglobulin E
Journal Article