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The Indian Journal of Pediatrics, ISSN 0019-5456, 10/2019, Volume 86, Issue 10, pp. 885 - 891
To report the distribution pattern of various categories of primary immunodeficiency disorders (PIDs) in children from North India, frequency of warning signs... 
Pediatrics | Severe combined immune deficiency | Medicine & Public Health | Primary immunodeficiencies | Gynecology | Hyper IgM syndrome | X-linked agammaglobulinemia | Common variable immune deficiency | Leukocyte adhesion deficiency | DHR
Journal Article
FRONTIERS IN IMMUNOLOGY, ISSN 1664-3224, 09/2019, Volume 10
Talaromyces (Penicillium) marneffei is an AIDS-defining infection in Southeast Asia and is associated with high mortality. It is rare in non-immunosuppressed... 
CD40L | STAT1 | DISSEMINATED COCCIDIOIDOMYCOSIS | IMMUNOLOGY | X-linked hyper-IgM syndrome | Taloromyces marneffei | flow cytometry | interferon gamma receptor deficiency | ADULT-ONSET IMMUNODEFICIENCY | DISSEMINATED HISTOPLASMOSIS | PATIENT | MUTATIONS | PENICILLIUM-MARNEFFEI | T-CELLS | HYPER-IGM | SIGNAL TRANSDUCER
Journal Article
Journal de Mycologie Médicale, ISSN 1156-5233, 09/2019, Volume 29, Issue 3, pp. 273 - 277
Following a fatal case of Cryptococcus neoformans meningitis in a child with X-linked hyper-immunoglobulin M syndrome (XHIGM), we evaluated the fungal isolate... 
Cryptococcus neoformans | Opportunistic infection | Hyper-IgM syndrome
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 06/2019, Volume 143, Issue 6, pp. 2238 - 2253
Journal Article
Human Immunology, ISSN 0198-8859, 06/2019, Volume 80, Issue 6, pp. 351 - 362
Primary B-cell immunodeficiencies refer to diseases resulting from impaired antibody production due to either molecular defects intrinsic to B-cells or a... 
Hyper IgM syndrome | Common variable immunodeficiency | B-cell receptor | Antibody | Agammaglobulinemia | Tyrosine | Medical colleges | Pyrimidines | Medical genetics | Biochemical genetics | B cells | Immunoglobulin A | T cells | Health aspects | Mitogens
Journal Article
Expert Review of Clinical Immunology, ISSN 1744-666X, 05/2019, Volume 15, Issue 5, pp. 461 - 486
Journal Article
EXPERT REVIEW OF CLINICAL IMMUNOLOGY, ISSN 1744-666X, 05/2019, Volume 15, Issue 5, pp. 529 - 540
Introduction: CD40 ligand (CD40L) deficiency or X-linked Hyper-IgM syndrome is a severe primary immunodeficiency caused by mutations in the CD40L gene. Despite... 
PRIMARY IMMUNE-DEFICIENCY | treatment | GENETIC-ANALYSIS | COLONY-STIMULATING FACTOR | HYPER-IGM SYNDROME | INTERFERON-GAMMA THERAPY | IMMUNOGLOBULIN THERAPY | IMMUNOLOGY | DEFECTIVE EXPRESSION | BONE-MARROW TRANSPLANTATION | CD40 ligand | primary immunodeficiency | X-LINKED IMMUNODEFICIENCY | STEM-CELL TRANSPLANTATION | CD40L deficiency
Journal Article
Journal Article
Clinical Immunology, ISSN 1521-6616, 03/2019, Volume 200, pp. 55 - 63
Ataxia-Telangiectasia (AT) is an immunodeficiency most often associated with T cell abnormalities. We describe a patient with a hyper-IgM phenotype and immune... 
γδ T cells | Hyper-IgM | Ataxia-telangiectasia | CD38loCD21−/low B cells | Tregs | Tfh | Fas | T-bet | CD38 | B cells | CD21 | REPERTOIRE | ACTIVATION | gamma delta T cells | CD38(lo)CD21(-/low) B cells | COMMON VARIABLE IMMUNODEFICIENCY | RECEPTOR | ALPHA | IMMUNOLOGY | DEFICIENCY | ACCUMULATION | T-CELLS | CD21(-/LOW) B-CELLS | Genetic aspects | T cells | Analysis
Journal Article