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301 results

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Page 1
Autoimmune polyendocrine syndrome type 1: Clinical manifestations, pathogenetic features, and management approach.
Bjørklund G, Pivin M, Hangan T, Yurkovskaya O, Pivina L. Bjørklund G, et al. Autoimmun Rev. 2022 Aug;21(8):103135. doi: 10.1016/j.autrev.2022.103135. Epub 2022 Jun 9. Autoimmun Rev. 2022. PMID: 35690244 Review.
Autoimmune polyendocrine syndrome type 1 (APS-1) is an autosomal recessive hereditary pathology that develops with endocrine and non-endocrine manifestations in childhood. ...APS-1 occurs because of mutations in the autoimmune regulator (AIRE) gene, leading to a dis
Autoimmune polyendocrine syndrome type 1 (APS-1) is an autosomal recessive hereditary pathology that develops with endocrine and non-
Polyglandular autoimmune syndromes.
Kahaly GJ, Frommer L. Kahaly GJ, et al. J Endocrinol Invest. 2018 Jan;41(1):91-98. doi: 10.1007/s40618-017-0740-9. Epub 2017 Aug 17. J Endocrinol Invest. 2018. PMID: 28819917 Review.
METHODS: Review of the pertinent and current literature. RESULTS: Polyglandular autoimmune syndromes (PAS) are multifactorial diseases with at least two coexisting autoimmune-mediated endocrinopathies. PAS show a great heterogeneity of syndromes and manifest sequent …
METHODS: Review of the pertinent and current literature. RESULTS: Polyglandular autoimmune syndromes (PAS) are multifactorial disease …
Autoimmune Diseases in Patients with Premature Ovarian Insufficiency-Our Current State of Knowledge.
Szeliga A, Calik-Ksepka A, Maciejewska-Jeske M, Grymowicz M, Smolarczyk K, Kostrzak A, Smolarczyk R, Rudnicka E, Meczekalski B. Szeliga A, et al. Int J Mol Sci. 2021 Mar 5;22(5):2594. doi: 10.3390/ijms22052594. Int J Mol Sci. 2021. PMID: 33807517 Free PMC article. Review.
Most causes of POI remain undefined, however, it is estimated that anywhere from 4-30% of cases are autoimmune in origin. As the ovaries are a common target for autoimmune attacks, an autoimmune etiology of POI should always be considered, especially in the p …
Most causes of POI remain undefined, however, it is estimated that anywhere from 4-30% of cases are autoimmune in origin. As the ovar …
Autoimmune Polyendocrine Syndromes.
Husebye ES, Anderson MS, Kämpe O. Husebye ES, et al. N Engl J Med. 2018 Mar 22;378(12):1132-1141. doi: 10.1056/NEJMra1713301. N Engl J Med. 2018. PMID: 29562162 Free PMC article. Review. No abstract available.
Autoinmune polyendocrinopathy.
Fernández Miró M, Colom Comí C, Godoy Lorenzo R. Fernández Miró M, et al. Med Clin (Barc). 2021 Sep 10;157(5):241-246. doi: 10.1016/j.medcli.2021.02.004. Epub 2021 May 3. Med Clin (Barc). 2021. PMID: 33958142 Review. English, Spanish.
Pluriglandular autoimmune syndrome (APS) can affect multiple endocrine glands and is associated with other autoimmune diseases. ...SPA type 3 is characterized by autoimmune thyroid disease and other autoimmune disease, excluding Addison's disease and h …
Pluriglandular autoimmune syndrome (APS) can affect multiple endocrine glands and is associated with other autoimmune diseases …
Autoimmune Polyendocrinopathy.
Frommer L, Kahaly GJ. Frommer L, et al. J Clin Endocrinol Metab. 2019 Oct 1;104(10):4769-4782. doi: 10.1210/jc.2019-00602. J Clin Endocrinol Metab. 2019. PMID: 31127843
CONTEXT: This mini-review offers an update on the rare autoimmune polyendocrinopathy (AP) syndrome with a synopsis of recent developments. DESIGN AND RESULTS: Systematic search for studies related to pathogenesis, immunogenetics, screening, diagnosis, clinical spectrum, an …
CONTEXT: This mini-review offers an update on the rare autoimmune polyendocrinopathy (AP) syndrome with a synopsis of recent developm …
Autoimmune enteropathies.
Umetsu SE, Brown I, Langner C, Lauwers GY. Umetsu SE, et al. Virchows Arch. 2018 Jan;472(1):55-66. doi: 10.1007/s00428-017-2243-7. Epub 2017 Oct 11. Virchows Arch. 2018. PMID: 29022145 Review.
Autoimmune enteropathy (AIE) is a rare condition characterized by intractable diarrhea and immune-mediated injury of the intestinal mucosa. As the clinical and histopathologic manifestations of this disease are highly variable, its diagnosis is challenging for both clinici
Autoimmune enteropathy (AIE) is a rare condition characterized by intractable diarrhea and immune-mediated injury of the intestinal m
Autoimmune polyglandular diseases.
Kahaly GJ, Frommer L. Kahaly GJ, et al. Best Pract Res Clin Endocrinol Metab. 2019 Dec;33(6):101344. doi: 10.1016/j.beem.2019.101344. Epub 2019 Oct 4. Best Pract Res Clin Endocrinol Metab. 2019. PMID: 31606344 Review.
Autoimmune polyglandular diseases (APD) are defined as the presence of two autoimmune -induced endocrine failures. ...Considering the high incidence of one or more endocrinopathies in first-degree relatives of patients with APD, family members should be regularly sc
Autoimmune polyglandular diseases (APD) are defined as the presence of two autoimmune -induced endocrine failures. ...Consider
Aire.
Mathis D, Benoist C. Mathis D, et al. Annu Rev Immunol. 2009;27:287-312. doi: 10.1146/annurev.immunol.25.022106.141532. Annu Rev Immunol. 2009. PMID: 19302042 Review.
Mutations in the transcriptional regulator, Aire, cause APECED, a polyglandular autoimmune disease with monogenic transmission. Animal models of APECED have revealed that Aire plays an important role in T cell tolerance induction in the thymus, mainly by promoting ectopic …
Mutations in the transcriptional regulator, Aire, cause APECED, a polyglandular autoimmune disease with monogenic transmission. Anima …
The immunobiology and clinical features of type 1 autoimmune polyglandular syndrome (APS-1).
Guo CJ, Leung PSC, Zhang W, Ma X, Gershwin ME. Guo CJ, et al. Autoimmun Rev. 2018 Jan;17(1):78-85. doi: 10.1016/j.autrev.2017.11.012. Epub 2017 Nov 4. Autoimmun Rev. 2018. PMID: 29108822 Review.
Autoimmune Polyglandular Syndrome type 1 (APS-1) is a subtype of the autoimmune polyendocrine syndrome characterized by the simultaneous or sequential dysfunction of multiple endocrine or non-endocrine glands. ...In this review, we provide a detailed critical overvi
Autoimmune Polyglandular Syndrome type 1 (APS-1) is a subtype of the autoimmune polyendocrine syndrome characterized by the si
301 results