Classification of primary immunodeficiencies: Need for a revised approach?

Journal of Allergy and Clinical Immunology

Volumn 131, Issue 2, 2013, Pages 292-294

  Maggina, Paraskevi ^a   Gennery, Andrew R ^a,b  

^a Infectious Diseases Allergy   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

classification; combined immunodeficiency; Primary immunodeficiency; profound immunodeficiency; severe combined immunodeficiency

Indexed keywords

CD40 LIGAND; IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; INTERLEUKIN 2 RECEPTOR GAMMA; INTERLEUKIN 7 RECEPTOR; MANNAN BINDING LECTIN; RAG1 PROTEIN; RAG2 PROTEIN; STAT1 PROTEIN; T LYMPHOCYTE RECEPTOR; WISKOTT ALDRICH SYNDROME PROTEIN;

B LYMPHOCYTE; CRYPTOSPORIDIUM; DEVELOPMENTAL DISORDER; DISEASE PREDISPOSITION; DISEASE SEVERITY; DNA POLYMORPHISM; GAMMA DELTA T LYMPHOCYTE; GENE MUTATION; GENETIC DISORDER; GENOTYPE; HUMAN; IMMUNE DEFICIENCY; IMMUNE DYSREGULATION; IMMUNE RESPONSE; IMMUNOSURVEILLANCE; INFECTION; LOSS OF FUNCTION MUTATION; LUNG ALVEOLUS PROTEINOSIS; NONHUMAN; OMENN SYNDROME; OUTCOME ASSESSMENT; PHENOTYPE; PNEUMOCYSTIS JIROVECI; PRIORITY JOURNAL; REVIEW; SALMONELLOSIS; SCID MOUSE; WISKOTT ALDRICH SYNDROME; X LINKED AGAMMAGLOBULINEMIA;

EID: 84873406855     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2012.10.008     Document Type: Editorial

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