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1964
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1981 1
1991 1
1992 3
1994 4
1995 5
1996 4
1997 7
1998 5
1999 8
2000 11
2001 7
2002 16
2003 5
2004 11
2005 12
2006 6
2007 14
2008 10
2009 18
2010 15
2011 8
2012 11
2013 15
2014 10
2015 10
2016 9
2017 13
2018 14
2019 9
2020 9
2021 18
2022 8
2023 10
2024 8
2025 0

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291 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.
Type 3 autoimmune polyglandular syndrome (APS-3) or type 3 multiple autoimmune syndrome (MAS-3): an expanding galaxy.
Betterle C, Furmaniak J, Sabbadin C, Scaroni C, Presotto F. Betterle C, et al. J Endocrinol Invest. 2023 Apr;46(4):643-665. doi: 10.1007/s40618-022-01994-1. Epub 2023 Jan 7. J Endocrinol Invest. 2023. PMID: 36609775 Review.
BACKGROUND: The number of recognised distinct autoimmune diseases (AIDs) has progressively increased over the years with more than 100 being reported today. ...These combinations are collectively termed type 3 Autoimmune Polyglandular Syndrome (APS-3), also called t …
BACKGROUND: The number of recognised distinct autoimmune diseases (AIDs) has progressively increased over the years with more than 10 …
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 …
IPEX syndrome from diagnosis to cure, learning along the way.
Bacchetta R, Roncarolo MG. Bacchetta R, et al. J Allergy Clin Immunol. 2024 Mar;153(3):595-605. doi: 10.1016/j.jaci.2023.11.021. Epub 2023 Nov 30. J Allergy Clin Immunol. 2024. PMID: 38040040 Free article. Review.
These studies have refined our knowledge of this rare yet prototypic genetic autoimmune disease, advancing the diagnosis, broadening the clinical spectrum, and improving our understanding of the underlying immunologic mechanisms. ...
These studies have refined our knowledge of this rare yet prototypic genetic autoimmune disease, advancing the diagnosis, broadening …
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
Human autoantibodies neutralizing type I IFNs: From 1981 to 2023.
Bastard P, Gervais A, Le Voyer T, Philippot Q, Cobat A, Rosain J, Jouanguy E, Abel L, Zhang SY, Zhang Q, Puel A, Casanova JL. Bastard P, et al. Immunol Rev. 2024 Mar;322(1):98-112. doi: 10.1111/imr.13304. Epub 2024 Jan 9. Immunol Rev. 2024. PMID: 38193358 Review.
They have since been found in patients with diverse conditions and are even used as a diagnostic criterion in patients with autoimmune polyendocrinopathy syndrome type 1 (APS-1). However, their apparent lack of association with viral diseases, including shingles, led to wi …
They have since been found in patients with diverse conditions and are even used as a diagnostic criterion in patients with autoimmune
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
291 results