Novel primary immunodeficiencies relevant to internal medicine: Novel phenotypes

Journal of Internal Medicine

Volumn 266, Issue 6, 2009, Pages 502-506

  Marodi L ^a   Casanova, J L ^b,c  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b IMAGINE INSTITUTE   (France)

^c ROCKEFELLER UNIVERSITY   (United States)

Author keywords

Novel immunodeficiency phenotypes; Primary immunodeficiencies

Indexed keywords

GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR;

ALLERGY; AUTOIMMUNITY; COMPLEMENT SYSTEM; CROHN DISEASE; DISEASE ASSOCIATION; GENE MUTATION; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR DEFICIENCY; HEALTH CARE PERSONNEL; HEMOLYTIC UREMIC SYNDROME; HUMAN; IMMUNE DEFICIENCY; IMMUNE RESPONSE; IMMUNOPATHOGENESIS; IMMUNOPATHOLOGY; INFECTION; INTERNAL MEDICINE; LUNG ALVEOLUS PROTEINOSIS; MACROPHAGE ACTIVATION; NEOPLASM; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY;

ADULT; CROHN DISEASE; DELAYED DIAGNOSIS; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; HEMOLYTIC-UREMIC SYNDROME; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; PHENOTYPE; PULMONARY ALVEOLAR PROTEINOSIS;

EID: 70449374931     PISSN: 09546820     EISSN: 13652796     Source Type: Journal    
DOI: 10.1111/j.1365-2796.2009.02166.x     Document Type: Short Survey

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