Cited by 758Adrenal Hormones and DisordersImmunodeficiency and Autoimmune DisordersMyasthenia Gravis and Thymoma

The DOI matches its Crossref record; 341 of the 354 references it cites were found in a registry or an index.

Autoimmune Adrenal Insufficiency and Autoimmune Polyendocrine Syndromes: Autoantibodies, Autoantigens, and Their Applicability in Diagnosis and Disease Prediction

Betterle, Corrado, Dal Pra, Chiara, Mantero, Franco, Zanchetta, Renato·2002·Endocrine Reviews

Abstract

Recent progress in the understanding of autoimmune adrenal disease, including a detailed analysis of a group of patients with Addison's disease (AD), has been reviewed. Criteria for defining an autoimmune disease and the main features of autoimmune AD (history, prevalence, etiology, histopathology, clinical and laboratory findings, cell-mediated andhumoral immunity, autoantigens and their autoepitopes, genetics, animal models, associated autoimmune diseases, pathogenesis, natural history, therapy) have been described. Furthermore, the autoimmune polyglandular syndromes (APS) associated with AD (revised classification, animal models, genetics, natural history) have been discussed. Of Italian patients with primary AD (n = 317), 83% had autoimmune AD. At the onset, all patients with autoimmune AD (100%) had detectable adrenal cortex and/or steroid 21-hydroxylase autoantibodies. In the course of natural history of autoimmune AD, the presence of adrenal cortex and/or steroid 21-hydroxylase autoantibodies identified patients at risk to develop AD. Different risks of progression to clinical AD were found in children and adults, and three stages of subclinical hypoadrenalism have been defined. Normal or atrophic adrenal glands have been demonstrated by imaging in patients with clinical or subclinical AD. Autoimmune AD presented in four forms: as APS type 1 (13% of the patients), APS type 2 (41%), APS type 4 (5%), and isolated AD (41%). There were differences in genetics, age at onset…

Overview

Integrity signals

Registry

Crossref · 10.1210/edrv.23.3.0466

Cites

341 of 341 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Flagged first, then by citations

Show all 354 references

13 of the 354 references couldn’t be matched to a known paper.

Research works printed but not linked: 21

  1. Addison, 1855, On the constitutional and local effects of disease of the suprarenal capsules. In a collection of the published writing of the late Thomas Addison, M.D., physician to Guy’s Hospital. London: New Sydenham Society 1868. [, Reprinted in Medical Classics, 2, 244
  2. Trousseau, 1856, Bronze Addison’s disease., Arch Gen Med, 8, 478
  3. Guttman, 1930, Addison’s disease., Arch Pathol, 10, 742
  4. Betterle, 1989, Morbo di Addison: principali associazioni cliniche e descrizione della storia naturale della malattia., Ann Ital Med Int, 4, 195
  5. Asherson, 1988, A “primary” antiphospholipid syndrome?, J Rheumatol, 15, 1742
  6. Bottazzo, 1996, Adrenalitis, oophoritis and autoimmune polyglandular disease. In: Rich RR, Fleisher TA, Schwartz DB, Shearer WT, Strober W, eds. Clinical immunology. Principles and practice. St., Louis: Mosby; chap, 100, 1523
  7. Verghese, 1980, Decreased suppressor cell activity in patients with polyglandular failure., Clin Res, 28, 270
  8. Schmidt, 1926, Eine biglandulare Erkrankung (Nebennieren und Schilddrüse) bei Morbus Addisonii., Verh Dtsch Ges Pathol, 21, 212
  9. Claude, 1908, Insuffisance pluriglandulaire endocrinienne., J Physiol Pathol Gen, 10, 469
  10. Von Mayenburg, 1940, Uber “insulitis” bei diabetes., Schweiz Med Wochenschr, 71, 554
  11. Adams, 1956, Abnormal responses in the assay of thyrotropin., Proc Univ Otago Med School, 34, 11
  12. Betterle, 1991, Melanin-producing cell autoantibodies: predictive marker of autoimmune vitiligo., Arch Dermatol, 128, 123, 10.1001/archderm.1992.01680110137027 · DOI
  13. Pitkänen, 2000, The autoimmune regulator protein has transcriptional transactivating properties and interereacts with the common coactivator CREB-binding protein., Am Soc Biochem Mol Biol, 275, 16802
  14. Ludwig, 1975, HLA antigens in idiopathic Addison’s disease., Z Immunitatsforschung, 149, 423
  15. Bigazzi, 1970, Anticorpi anti-surrene nel morbo di Addison., Folia Allergol Immunol Clin, 17, 46
  16. Andrada, 1968, Serological investigation on Addison’s disease., Clin Sci, 206, 1535
  17. Pousset, 1970, Anticorps antisurrénaliens et maladie d’Addison., Ann Endocrinol (Paris), 31, 995
  18. Tanaka, 1997, Autoimmune adrenal diseases—a new sensitive assay for measurement of steroid 21-hydroxylase autoantibodies., J Clin Endocrinol Metab, 82, 1440
  19. Del Prete, 1976, Autoanticorpi nella menopausa precoce., Folia Allergol Immunol Clin, 23, 367
  20. Yu, 1999, DRB1*04 and DQ alleles: expressions of 21-hydroxylase autoantibodies and risk of progressions to Addison’s disease., J Clin Endocrinol Metab, 84, 328
  21. Auchus, 2001, The principles, pathways, and enzymes of human steroidogenesis, In De Groot LJ, Jameson JL, eds. Endocrinology, 4th ed. Philadelphia: WB Saunders Co.; chap, 115, 1616

Cited by

Sorted by citations

Items 701–756 of 756

Metadata

Authors
Betterle, C., Dal Pra, C., Mantero, F., & Zanchetta, R.
Affiliations
  • University of Padua (IT)
  • Chair of Clinical Immunology and Allergy (C.B., C.D.P., R.Z.), Department of Medical and Surgical Sciences, University of Padova, I-35128, Padova, Italy
Venue
Endocrine Reviews
Published
2002-06-01
Volume
23
Issue
3
Pages
327-364
ISSN
  • 0163-769X (ISSN-L)
  • 1945-7189
OpenAlex
W2125286421
Cited by
758
References
354
Citations by year
2026: 26 · 2025: 16 · 2024: 28 · 2023: 23 · 2022: 24 · 2021: 32 · 2020: 30 · 2019: 39 · 2018: 30 · 2017: 36 · 2016: 28 · 2015: 35 · 2014: 47 · 2013: 36 · 2012: 36
FWCI
4.26
Type
journal article
Language
en
Open access
closed
Locations
  • Endocrine Reviews (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Health Sciences › Medicine › Clinical Neurology › Myasthenia Gravis and Thymoma
Keywords
autoimmune adrenal insufficiency, Addison's disease, autoimmune polyglandular syndrome, autoantibodies, autoantigens, 21-hydroxylase, hypergonadotropic hypogonadism, adrenal imaging
MeSH terms
Adrenal Insufficiency, Autoantibodies, Autoantigens, Autoimmune Diseases, Humans, Prognosis, Polyendocrinopathies, Autoimmune

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review