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Volumn 34, Issue 4, 2014, Pages 459-468

First report on the Moroccan registry of primary immunodeficiencies: 15 Years of experience (1998-2012)

Author keywords

epidemiology; Morocco; Primary immunodeficiency; registry

Indexed keywords

ADULT; AGAMMAGLOBULINEMIA; ARTICLE; ATAXIA TELANGIECTASIA; AUTOINFLAMMATORY DISEASE; BACTERIAL ARTHRITIS; BARE LYMPHOCYTE SYNDROME; BONE MARROW TRANSPLANTATION; BRONCHIECTASIS; CANDIDIASIS; CHILD; CHRONIC DIARRHEA; CLINICAL FEATURE; COMBINED IMMUNODEFICIENCY; COMPLEMENT DEFICIENCY; CONSANGUINITY; DIAGNOSTIC ERROR; DISEASE COURSE; EPIDEMIOLOGICAL DATA; FAILURE TO THRIVE; FAMILY HISTORY; FEMALE; GENETIC SCREENING; HUMAN; HUMORAL IMMUNE DEFICIENCY; HYPER IGE SYNDROME; IMMUNE DEFICIENCY; IMMUNE DYSREGULATION; INFANT; INNATE IMMUNITY; LOWER RESPIRATORY TRACT INFECTION; MAJOR CLINICAL STUDY; MALE; MENINGITIS; MOROCCO; MORTALITY; ONSET AGE; OSTEOMYELITIS; PHAGOCYTE DYSFUNCTION; PREVALENCE; PRIORITY JOURNAL; REGISTER; SEPTICEMIA; SEVERE COMBINED IMMUNODEFICIENCY; SKIN INFECTION; UPPER RESPIRATORY TRACT INFECTION; URINARY TRACT INFECTION; ADOLESCENT; CLASSIFICATION; IMMUNOLOGIC DEFICIENCY SYNDROMES; MIDDLE AGED; NEWBORN; PRESCHOOL CHILD;

EID: 84901451026     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-014-0005-8     Document Type: Article
Times cited : (50)

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