Primary immunodeficiency diseases in Norway

Journal of Clinical Immunology

Volumn 20, Issue 6, 2000, Pages 477-485

  Stray Pedersen, Asbjørg ^a   Abrahamsen, Tore G ^a   Frøland, Stig S ^a  

^a UNIVERSITY OF OSLO   (Norway)

Author keywords

Norway; Primary immunodeficiency; Registry

Indexed keywords

IMMUNOGLOBULIN A;

ADULT; ANGIONEUROTIC EDEMA; ARTICLE; CHILD; COMBINED IMMUNODEFICIENCY; COMPLEMENT DEFICIENCY; FEMALE; HEALTH SURVEY; HUMAN; HUMORAL IMMUNE DEFICIENCY; IMMUNE DEFICIENCY; MAJOR CLINICAL STUDY; MALE; NORWAY; PREVALENCE; PRIORITY JOURNAL; QUESTIONNAIRE; REGISTER;

ADULT; CHILD; COMPLEMENT SYSTEM PROTEINS; FEMALE; HUMANS; IMMUNOGLOBULINS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INCIDENCE; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MALE; NORWAY; PHAGOCYTE BACTERICIDAL DYSFUNCTION; PREVALENCE;

EID: 0034493406     PISSN: 02719142     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1026416017763     Document Type: Article

References (44)

1. Report from the ESID Registry of Primary Immunodeficiencies
2. Primary immunodeficiency register, United Kingdom: Update 1992
3. Primary immunodeficiency register, United Kingdom 1998
4. Primary immunodeficiency disorders in Sweden: Cases among children 1974-1979
5. Primary immunodeficiencies in Switzerland: First report of the national registry in adults and children
6. Registry of primary immunodeficiencies in Switzerland
7. Primary immunodeficiencies in Italy. Data revised from the Italian Register of Immunodeficiencies-IRID (1977-1988)
8. Primary immunodeficiency syndromes in Italy: A report of the national register in children and adults
9. Primary immunodeficiency syndrome in Spain: First report of the National Registry in children and adults
10. Primary immunodeficiency syndrome in Japan. I. Overview of a national-wide survey on primary immunodeficiency
11. Primary antibody deficiency in Arabs: First report from eastern Saudi Arabia
12. The spectrum of primary immunodeficiency disorders in Australia
13. Primary immunodeficiency diseases in Latin America: First report from eight countries participating in the LAGID. Latin American Group for primary Immunodeficiency Diseases
14. Immunodeficiency mutation databases - A new research tool
15. BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
16. Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 Unique mutations without correlation to clinical course
17. WASPbase: A database of WAS- and XLT-causing mutations
18. Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: Identification of twelve different mutations in the WASP gene
19. Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency
20. CD401base: A database of CD40L gene mutations causing X-linked hyper-IgM syndrome
21. X-CGDbase: A database of X-CGD-causing mutations
22. Report on the United States Registry of patients with chronic granulomatous disease (CGD)
23. Pathophysiology and treatment of severe chronic neutropenia
24. A multi-institutional survey of the Wiskott-Aldrich syndrome
25. Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants
26. Clinical spectrum of X-linked hyper IgM syndrome
27. Primary immunodeficiency diseases. Report of a WHO scientific group
28. Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: Evidence for a founder effect
29. Hereditary angio-oedema: New clinical observations and autoimmune screening, complement and kallikrein-kinin analyses
30. Genetic aspects of complement component C8 in Norwegian meningococcal disease patients
31. Low prevalence of complement deficiencies among patients with meningococcal disease in Norway
32. Prevalence of a mutation causing C2 deficiency in systemic lupus erytrematousus
33. Familial disseminated infection due to atypical mycobacteria with childhood onset
34. Transient B cell immaturity with intractable diarrhoea: A possible new immunodeficiency syndrome
35. Hyper-IgE syndrome with recurrent infections - An autosomal dominant multisystem disorder
36. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients
37. An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
38. Chronic mucocutaneous candidiasis: Immunologic studies of three generations of a single family
39. Wiscott-Aldrich syndome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype
40. Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden