Organ-specific and non-organ-specific autoantibodies in children and young adults with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)

European Journal of Endocrinology

Volumn 143, Issue 4, 2000, Pages 497-503

  Perniola, R ^a   Falorni, A ^a   Clemente, M G ^a   Forini, F ^a   Accogli, E ^a   Lobreglio, G ^a  

^a NONE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINUCLEAR ANTIBODY; AUTOANTIBODY; AUTOIMMUNE POL; C PEPTIDE; CHOLESTEROL MONOOXYGENASE (SIDE CHAIN CLEAVING); CYTOCHROME P450; ENZYME ANTIBODY; GLUTAMATE DECARBOXYLASE; INTRINSIC FACTOR; ISOENZYME; LIVER ENZYME; MICROSOME ANTIBODY; STEROID 17ALPHA MONOOXYGENASE; STEROID 21 MONOOXYGENASE; THYROGLOBULIN ANTIBODY; THYROID PEROXIDASE; THYROTROPIN RECEPTOR; UNCLASSIFIED DRUG;

ADDISON DISEASE; ADOLESCENT; ADRENAL CORTEX; ADULT; ARTICLE; ATROPHIC GASTRITIS; AUTOIMMUNE DISEASE; AUTOIMMUNE HEPATITIS; AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE MARKER; FEMALE; HUMAN; HYPOGONADISM; HYPOTHYROIDISM; IMMUNOBLOTTING; IMMUNOFLUORESCENCE TEST; IMMUNORADIOMETRIC ASSAY; INSULIN DEPENDENT DIABETES MELLITUS; ITALY; MALABSORPTION; MALE; OVARY; PANCREAS ISLET CELL; PARATHYROID GLAND; PERNICIOUS ANEMIA; PRIORITY JOURNAL; STOMACH PARIETAL CELL; TESTIS;

EID: 0033772333     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1430497     Document Type: Article

References (44)

1. An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-linger domains
2. Polyglandular autoimmune syndromes
3. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients
4. Autoimmune polyglandular syndrome type 1
5. Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease
6. Autoantibodies to steroidogenic enzymes in autoimmune polyglandular syndrome, Addison's disease, and premature ovarian failure
7. Immunoprecipitation of steroidogenic enzyme autoantigens with autoimmune polyglandular syndrome type I (APS I) sera; further evidence for independent humoral immunity to P450c17 and P450c21
8. Autoantibodies against a novel 51 kDa islet antigen and glutamate decarboxylase isoforms in autoimmune polyendocrine syndrome type I
9. Antibodies to glutamic acid decarboxylase and insulin-dependent diabetes in patients with autoimmune polyendocrine syndrome type I
10. Glutamic acid decarboxylase (GAD) in insulin-dependent diabetes mellitus
11. Two cytochromes P450 are major hepatocellular autoantigens in autoimmune polyglandular syndrome type 1
12. Multiple autoantigens in the prediction and pathogenesis of type I diabetes
13. Autoimmune thyroid disease: Further developments in our understanding
14. Meeting report: International Autoimmune Hepatitis Group
15. Preliminary criteria for the classification of Sjogren's syndrome
16. High diagnostic accuracy for idiopathic Addison's disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase
17. 3H recombinant human ligands
18. Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17α-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
19. The APECED polyglandular autoimmune syndrome protein, AIRE-1, contains the SAND domain and is probably a transcription factor
20. APECED: A monogenic autoimmune disease providing new clues to self-tolerance
21. Identification by molecular cloning of an autoantigen associated with Addison's disease as steroid 17α-hydroxylase
22. Two different cytochrome P450 enzymes are the adrenal antigens in autoimmune polyendocrine syndrome type I and Addison's disease
23. Characterization of adrenal autoantigens recognized by sera from patients with autoimmune polyglandular syndrome (APS) type I
24. 21-Hydroxylase autoantibodies in adult patients with endocrine autoimmune diseases are highly specific for Addison's disease
25. Progression to type I diabetes in autoimmune endocrine patients with islet cell antibodies
26. Slow metabolic deterioration towards diabetes in islet cell antibody positive patients with autoimmune polyendocrine disease
27. Antibodies to islet 37k antigen, but not to glutamate decarboxylase, discriminate rapid progression to IDDM in endocrine autoimmunity
28. Anti-thyroglobulin autoantibodies in autoimmune thyroid diseases: Cross-reactive or pathogenic?
29. Juvenile familial endocrinopathy
30. Chronic mucocutaneous candidiasis, endocrine deficiency and alopecia areata
31. Selective hypopituitarism. Impaired cell-mediated immunity and chronic mucocutaneous candidiasis
32. Familial chronic idiopathic hypoparathyroidism associated with rheumatoid arthritis
33. Variable cell-mediated immune defects in a family with 'Candida endocrinopathy syndrome'
34. Poliendocrinopatia autoimmune. Studio immunologico
35. The polyglandular failure syndrome: Disease inheritance, HLA type, and immune function
36. Evidence for defective immunoregulation in the syndrome of familial candidiasis endocrinopathy
37. Polyendocrinopathie auto-immune et candidose mucocutanee chronique
38. Pure red cell hypoplasia associated with polyglandular autoimmune syndrome type I
39. Intestinal lymphangiectasia in a patient with autoimmune polyglandular disease type I and steatorrhea
40. Pure red cell aplasia in autoimmune polyglandular syndrome with T lymphocytosis
41. Detection and identification of antinuclear autoantibodies in the serum of normal blood donors
42. The prevalence of antinuclear antibodies in healthy young persons and adults, comparing rat liver tissue sections with HEp-2 cells as antigen substrate
43. Range of antinuclear antibodies in 'healthy' individuals
44. The frequency of antinuclear antibody (ANA) in children by use of mouse kidney (MK) and human epithelial cells (HEp-2) as substrates