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Volumn 114, Issue 3, 2004, Pages 677-687
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Primary immunodeficiency diseases: An update
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d
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d,f
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Author keywords
B cells; complement; immune dysregulation syndromes; innate immunity; phagocytes; Primary immunodeficiency diseases; T cells
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Indexed keywords
ACTIVATION INDUCED CYTIDINE DEAMINASE DEFICIENCY;
ADENOSINE DEAMINASE DEFICIENCY;
ARTEMIS DEFICIENCY;
ATAXIA LIKE SYNDROME;
ATAXIA TELANGIECTASIA;
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME;
AUTOSOMAL RECESSIVE AGAMMAGLOBULINEMIA;
AUTOSOMAL X LINKED CHRONIC GRANULOMATOUS DISEASE;
BETA ACTIN DEFICIENCY;
BLOOM SYNDROME;
CASPASE 10 DEFECT;
CASPASE 8 DEFECT;
CD3 DELTA GENE DEFICIENCY;
CD3 EPSILON GENE DEFICIENCY;
CD40 GENE DEFICIENCY;
CD45 GENE DEFICIENCY;
CD8 DEFICIENCY;
CD95 DEFECT;
CD95 LIGAND DEFECT;
CELLULAR IMMUNITY;
CHEDIAK HIGASHI SYNDROME;
CHRONIC GRANULOMATOUS DISEASE;
COMMON VARIABLE IMMUNODEFICIENCY;
CONFERENCE PAPER;
DEOXYRIBONUCLEIC ACID LIGASE IV DEFICIENCY;
DIGEORGE SYNDROME;
GAMMA CHAIN DEFICIENCY;
GENE MUTATION;
GENETICS;
GRISCELLI SYNDROME;
GRISCELLI SYNDROME 2;
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS;
HUMAN;
HUMORAL IMMUNITY;
IMMUNE DEFICIENCY;
IMMUNE SYSTEM;
IMMUNOGLOBULIN A DEFICIENCY;
IMMUNOGLOBULIN G DEFICIENCY;
IMMUNOGLOBULIN HEAVY CHAIN GENE DELETION DEFICIENCY;
INDUCIBLE COSTIMULATOR DEFICIENCY;
INFECTION;
INTERFERON GAMMA RECEPTOR DEFICIENCY;
INTERLEUKIN 12 PROTEIN P40 DEFICIENCY;
INTERLEUKIN 12 RECEPTOR DEFICIENCY;
INTERLEUKIN 23 RECEPTOR DEFICIENCY;
INTERLEUKIN 7 RECEPTOR ALPHA DEFICIENCY;
JAK3 DEFICIENCY;
KAPPA CHAIN DEFICIENCY;
KERATOSIS PALMOPLANTARIS;
LEUKOCYTE ADHESION DEFICIENCY 1;
LEUKOCYTE ADHESION DEFICIENCY 2;
LEUKOCYTE ADHESION DEFICIENCY 3;
LOCALIZED JUVENILE PERIODONTITIS;
MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2 DEFICIENCY;
MUNC GENE DEFICIENCY;
MYELODYSPLASIA;
MYELOPEROXIDASE DEFICIENCY;
NEUTROPENIA;
NEUTROPHIL GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY;
NIJMEGEN BREAKAGE SYNDROME;
OMENN SYNDROME;
PERFORIN DEFICIENCY;
PORTUGAL;
PRIORITY JOURNAL;
PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY;
RAC 2 PROTEIN DEFICIENCY;
RECOMBINASE ACTIVATION GENE 1 DEFICIENCY;
RECOMBINASE ACTIVATION GENE 2 DEFICIENCY;
RETICULAR DYSGENESIS;
SELECTIVE IMMUNOGLOBULIN DEFICIENCY;
SEVERE CONGENITAL NEUTROPENIA;
SHWACHMAN SYNDROME;
SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 DEFICIENCY;
SPECIFIC ANTIBODY DEFICIENCY;
SPECIFIC GRANULE DEFICIENCY;
TRANSIENT HYPOGAMMAGLOBULINEMIA OF INFANCY;
TRANSPORTER ASSOCIATED PROTEIN 1 DEFICIENCY;
TRANSPORTER ASSOCIATED PROTEIN 2 DEFICIENCY;
URACIL DEOXYRIBONUCLEIC ACID GLYCOSYLASE DEFICIENCY;
WINGED HELIX NUDE DEFICIENCY;
WISKOTT ALDRICH SYNDROME;
WORLD HEALTH ORGANIZATION;
X LINKED AGAMMAGLOBULINEMIA;
X LINKED CHRONIC GRANULOMATOUS DISEASE;
X LINKED HYPERIMMUNOGLOBULIN M SYNDROME;
X LINKED LYMPHOPROLIFERATIVE SYNDROME;
X LINKED NEUTROPENIA;
ZETA ASSOCIATED PROTEIN 70 DEFICIENCY;
ANIMALS;
ANTIBODY FORMATION;
GENE EXPRESSION REGULATION;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
IMMUNITY, CELLULAR;
IMMUNITY, NATURAL;
IMMUNOLOGIC DEFICIENCY SYNDROMES;
INTERNATIONAL COOPERATION;
MICE;
MICE, KNOCKOUT;
MUTATION;
SOCIETIES, SCIENTIFIC;
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EID: 4444379717
PISSN: 00916749
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jaci.2004.06.044 Document Type: Conference Paper |
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Times cited : (172)
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References (4)
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