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Volumn 173, Issue 2, 2013, Pages 372-380
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The German national registry for primary immunodeficiencies (PID)
a a a b b a a c c c c b b d d e e f g h more.. |
Author keywords
chronic granulomatous disease (CGD); common variable immunodeficiency (CVID); DiGeorge syndrome; immunodeficiency primary; X linked agammaglobulinaemia (XLA)
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Indexed keywords
BRONCHODILATING AGENT;
IMMUNOGLOBULIN;
IMMUNOSUPPRESSIVE AGENT;
AGAMMAGLOBULINEMIA;
AGE DISTRIBUTION;
ARTICLE;
ATAXIA TELANGIECTASIA;
AUTOINFLAMMATORY DISEASE;
BONE MARROW TRANSPLANTATION;
CHRONIC GRANULOMATOUS DISEASE;
CLINICAL RESEARCH;
COMMON VARIABLE IMMUNODEFICIENCY;
CONSANGUINITY;
DATA BASE;
DELAYED DIAGNOSIS;
DIGEORGE SYNDROME;
DISEASE REGISTRY;
FOLLOW UP;
FUNDING;
GENDER;
GEOGRAPHIC DISTRIBUTION;
GERMANY;
HEMOPHAGOCYTIC SYNDROME;
HUMAN;
IMMUNE DEFICIENCY;
IMMUNOGLOBULIN DEFICIENCY;
MEDICAL ETHICS;
MEDICAL SOCIETY;
MOLECULAR DIAGNOSIS;
NONHUMAN;
PREVALENCE;
PRIORITY JOURNAL;
WISKOTT ALDRICH SYNDROME;
X LINKED AGAMMAGLOBULINEMIA;
CHRONIC GRANULOMATOUS DISEASE (CGD);
COMMON VARIABLE IMMUNODEFICIENCY (CVID);
DIGEORGE SYNDROME;
IMMUNODEFICIENCY-PRIMARY;
X-LINKED AGAMMAGLOBULINAEMIA (XLA);
ADOLESCENT;
ADULT;
AGE FACTORS;
AGED;
CHILD;
CHILD, PRESCHOOL;
DATABASES, FACTUAL;
FEMALE;
GERMANY;
HUMANS;
IMMUNOLOGIC DEFICIENCY SYNDROMES;
INFANT;
INFANT, NEWBORN;
MALE;
MIDDLE AGED;
PREVALENCE;
REGISTRIES;
YOUNG ADULT;
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EID: 84879999199
PISSN: 00099104
EISSN: 13652249
Source Type: Journal
DOI: 10.1111/cei.12105 Document Type: Article |
Times cited : (66)
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References (9)
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