PubMed for id: 1788942

Year	Number of Results
1971	1
1975	1
1977	2
1978	1
1980	1
1981	2
1982	3
1984	1
1985	4
1986	2
1987	3
1988	2
1989	3
1990	3
1991	6
1992	4
1993	2
1995	2
1996	2
1997	1
1998	1
1999	2
2000	7
2001	6
2002	3
2003	1
2004	7
2005	7
2006	10
2007	8
2008	11
2009	11
2010	9
2011	14
2012	11
2013	19
2014	11
2015	22
2016	14
2017	24
2018	24
2019	20
2020	19
2021	24
2022	23
2023	11

1

Case Report: Eosinophilic gastritis with pyloric stenosis in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Yu R, Xiao Y, Xu W, Zhang T, Wang Y, Hu H. Yu R, et al. Front Pediatr. 2022 Nov 21;10:1039341. doi: 10.3389/fped.2022.1039341. eCollection 2022. Front Pediatr. 2022. PMID: 36479284 Free PMC article.

2

Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.

Huang Y, Fang S, Zeng T, Chen J, Yang L, Sun G, Dai R, An Y, Tang X, Dou Y, Zhao X, Zhou L. Huang Y, et al. Front Immunol. 2022 Aug 24;13:972746. doi: 10.3389/fimmu.2022.972746. eCollection 2022. Front Immunol. 2022. PMID: 36091011 Free PMC article.

3

Identification of a novel variant of FOXP3 resulting in severe immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome highlights potential pitfalls of molecular testing.

Kirchner A, Sanchez IM, Zalan A, Bhat G, Bain M. Kirchner A, et al. Pediatr Dermatol. 2022 May;39(3):483-485. doi: 10.1111/pde.14936. Epub 2022 Feb 22. Pediatr Dermatol. 2022. PMID: 35191551

4

Cow's milk allergy non-responsive to amino acid-based formula? A successful transplanted patient with immune dysregulation, polyendocrinopathy, enteropathy, and X-linked syndrome.

Veramendi-Espinoza L, Rentería-Valdiviezo CA, Díaz-Subauste R, Aldave-Becerra JC, Alva-Lozada G, Becilli M, Locatelli F. Veramendi-Espinoza L, et al. Clin Case Rep. 2021 Oct 5;9(10):e04900. doi: 10.1002/ccr3.4900. eCollection 2021 Oct. Clin Case Rep. 2021. PMID: 34631084 Free PMC article.

5

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome Manifesting as Lymphocytic Interstitial Pneumonia and Treatment-Resistant Bullous Pemphigoid.

Andersen SM, Fage S, Rubak SL, Holm M, Jensen JMB, Mogensen T, Deleuran M. Andersen SM, et al. Pediatr Allergy Immunol Pulmonol. 2021 Jun;34(2):76-79. doi: 10.1089/ped.2020.1307. Pediatr Allergy Immunol Pulmonol. 2021. PMID: 34143686 Free PMC article.

6

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Syndrome in Two Siblings: Same Mutation But Different Clinical Manifestations at Onset.

Karagüzel G, Polat R, Abul MH, Cebi AH, Orhan F. Karagüzel G, et al. J Clin Res Pediatr Endocrinol. 2022 Aug 25;14(3):361-365. doi: 10.4274/jcrpe.galenos.2021.2021.0005. Epub 2021 May 28. J Clin Res Pediatr Endocrinol. 2022. PMID: 34044499 Free PMC article.

7

[Clinical features and genetic analysis of a child with late-onset immune dysregulation, polyendocrinopathy, enteropathy, X-Linked syndrome].

Zhou F, Wang R, Yu Z, Li S, Li X. Zhou F, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Mar 10;38(3):255-259. doi: 10.3760/cma.j.cn511374-20200420-00289. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33751536 Review. Chinese.

8

New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and Duodenum.

Duztas DT, Al-Shadfan L, Ozturk H, Yazan H, Cakir E, Ekinci NUO, Dalgic B, Rohlfs M, Jeske T, Klein C, Kotlarz D, Gurkan OE. Duztas DT, et al. Pediatr Dev Pathol. 2021 May-Jun;24(3):252-257. doi: 10.1177/1093526621998868. Epub 2021 Mar 8. Pediatr Dev Pathol. 2021. PMID: 33683986

9

An X-linked syndrome with severe neurodevelopmental delay, hydrocephalus, and early lethality caused by a missense variation in the OTUD5 gene.

Tripolszki K, Sasaki E, Hotakainen R, Kassim AH, Pereira C, Rolfs A, Bauer P, Reardon W, Bertoli-Avella AM. Tripolszki K, et al. Clin Genet. 2021 Feb;99(2):303-308. doi: 10.1111/cge.13873. Epub 2020 Nov 9. Clin Genet. 2021. PMID: 33131077

10

Early-onset refractory diarrhea due to immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome associated with a novel mutation in the FOXP3 gene: A case report.

Su N, Chen C, Zhou X, Ma GD, Chen RL, Tian C. Su N, et al. World J Clin Cases. 2020 May 26;8(10):1988-1994. doi: 10.12998/wjcc.v8.i10.1988. World J Clin Cases. 2020. PMID: 32518791 Free PMC article.

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