These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
188 related articles for article (PubMed ID: 31269558)
1. [A case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome with very early onset inflammatory bowel disease-like changes]. Bao WT; Li ZL; Li J; Shi XY; Zhang J; Wu H Zhonghua Er Ke Za Zhi; 2019 Jul; 57(7):559-561. PubMed ID: 31269558 [TBL] [Abstract][Full Text] [Related]
3. Nonclassic Inflammatory Bowel Disease in Young Infants: Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome, and Other Disorders. Chandrakasan S; Venkateswaran S; Kugathasan S Pediatr Clin North Am; 2017 Feb; 64(1):139-160. PubMed ID: 27894441 [TBL] [Abstract][Full Text] [Related]
4. Extremely Early Onset IPEX Syndrome Caused by a Novel Small Exonic Deletion in FOXP3. Smith E; Greeley SA; Ye H; Torgerson TR; Dimmitt R; Atkinson P; Philips J; Goldman F J Pediatr Gastroenterol Nutr; 2016 Nov; 63(5):e119-e120. PubMed ID: 25187107 [No Abstract] [Full Text] [Related]
5. Anti-voltage-Gated Potassium Channel (VGKC) Antibodies and Acquired Neuromyotonia in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy X-Lined (IPEX) Syndrome. Moseley N; King J; Van Dort B; Williams S; Rodriguez-Casero V; Ramachandran S; Choo S; Cole T; McLean-Tooke A J Clin Immunol; 2021 Nov; 41(8):1972-1974. PubMed ID: 34478044 [No Abstract] [Full Text] [Related]
6. Autoimmune Polyendocrine Syndromes. Husebye ES; Anderson MS; Kämpe O N Engl J Med; 2018 Mar; 378(12):1132-1141. PubMed ID: 29562162 [No Abstract] [Full Text] [Related]
7. Lichenoid Dermatitis in an Adult with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome. Choi YM; Wang YT; Geng B; Garcia-Lloret M; Smart CN Skinmed; 2017; 15(3):231-234. PubMed ID: 28705291 [TBL] [Abstract][Full Text] [Related]
8. Persistent Enteropathy in a Toddler with a Novel FOXP3 Mutation and Normal FOXP3 Protein Expression. Seghezzo S; Bleesing JJ; Kucuk ZY J Pediatr; 2017 Jul; 186():183-185. PubMed ID: 28457527 [TBL] [Abstract][Full Text] [Related]
9. From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation. Bacchetta R; Barzaghi F; Roncarolo MG Ann N Y Acad Sci; 2018 Apr; 1417(1):5-22. PubMed ID: 26918796 [TBL] [Abstract][Full Text] [Related]
10. Lentiviral Gene Therapy in HSCs Restores Lineage-Specific Foxp3 Expression and Suppresses Autoimmunity in a Mouse Model of IPEX Syndrome. Masiuk KE; Laborada J; Roncarolo MG; Hollis RP; Kohn DB Cell Stem Cell; 2019 Feb; 24(2):309-317.e7. PubMed ID: 30639036 [TBL] [Abstract][Full Text] [Related]
11. Opinion and Special Articles: Cerebellar Ataxia and Liver Failure Complicating IPEX Syndrome. Rim J; Byler M; Soldatos A; Notarangelo L; Leibovitch E; Jacobson S; Gorman M; Lebel RR; Werner K Neurology; 2021 Feb; 96(6):e956-e959. PubMed ID: 33168705 [No Abstract] [Full Text] [Related]
12. Quantitative analysis of tissue inflammation and responses to treatment in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome, and review of literature. Chen CA; Chung WC; Chiou YY; Yang YJ; Lin YC; Ochs HD; Shieh CC J Microbiol Immunol Infect; 2016 Oct; 49(5):775-782. PubMed ID: 26748735 [TBL] [Abstract][Full Text] [Related]
13. The immunological and genetic basis of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. Bin Dhuban K; Piccirillo CA Curr Opin Allergy Clin Immunol; 2015 Dec; 15(6):525-32. PubMed ID: 26485097 [TBL] [Abstract][Full Text] [Related]
14. Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management. Baxter SK; Walsh T; Casadei S; Eckert MM; Allenspach EJ; Hagin D; Segundo G; Lee MK; Gulsuner S; Shirts BH; Sullivan KE; Keller MD; Torgerson TR; King MC J Allergy Clin Immunol; 2022 Jan; 149(1):327-339. PubMed ID: 33864888 [TBL] [Abstract][Full Text] [Related]
15. Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound. Louie RJ; Tan QK; Gilner JB; Rogers RC; Younge N; Wechsler SB; McDonald MT; Gordon B; Saski CA; Jones JR; Chapman SJ; Stevenson RE; Sleasman JW; Friez MJ Am J Med Genet A; 2017 May; 173(5):1219-1225. PubMed ID: 28317311 [TBL] [Abstract][Full Text] [Related]