361 related articles for article (PubMed ID: 32234571)
1. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: A systematic review.
Park JH; Lee KH; Jeon B; Ochs HD; Lee JS; Gee HY; Seo S; Geum D; Piccirillo CA; Eisenhut M; van der Vliet HJ; Lee JM; Kronbichler A; Ko Y; Shin JI
Autoimmun Rev; 2020 Jun; 19(6):102526. PubMed ID: 32234571
[TBL] [Abstract][Full Text] [Related]
2. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases.
Verbsky JW; Chatila TA
Curr Opin Pediatr; 2013 Dec; 25(6):708-14. PubMed ID: 24240290
[TBL] [Abstract][Full Text] [Related]
3. The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome.
d'Hennezel E; Bin Dhuban K; Torgerson T; Piccirillo CA
J Med Genet; 2012 May; 49(5):291-302. PubMed ID: 22581967
[TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.
Gambineri E; Perroni L; Passerini L; Bianchi L; Doglioni C; Meschi F; Bonfanti R; Sznajer Y; Tommasini A; Lawitschka A; Junker A; Dunstheimer D; Heidemann PH; Cazzola G; Cipolli M; Friedrich W; Janic D; Azzi N; Richmond E; Vignola S; Barabino A; Chiumello G; Azzari C; Roncarolo MG; Bacchetta R
J Allergy Clin Immunol; 2008 Dec; 122(6):1105-1112.e1. PubMed ID: 18951619
[TBL] [Abstract][Full Text] [Related]
5. Molecular feature and therapeutic perspectives of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Huang Q; Liu X; Zhang Y; Huang J; Li D; Li B
J Genet Genomics; 2020 Jan; 47(1):17-26. PubMed ID: 32081609
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.
Gambineri E; Ciullini Mannurita S; Hagin D; Vignoli M; Anover-Sombke S; DeBoer S; Segundo GRS; Allenspach EJ; Favre C; Ochs HD; Torgerson TR
Front Immunol; 2018; 9():2411. PubMed ID: 30443250
[No Abstract] [Full Text] [Related]
8. Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.
Uzel G; Sampaio EP; Lawrence MG; Hsu AP; Hackett M; Dorsey MJ; Noel RJ; Verbsky JW; Freeman AF; Janssen E; Bonilla FA; Pechacek J; Chandrasekaran P; Browne SK; Agharahimi A; Gharib AM; Mannurita SC; Yim JJ; Gambineri E; Torgerson T; Tran DQ; Milner JD; Holland SM
J Allergy Clin Immunol; 2013 Jun; 131(6):1611-23. PubMed ID: 23534974
[TBL] [Abstract][Full Text] [Related]
9. Mechanistic associations of a mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome.
De Benedetti F; Insalaco A; Diamanti A; Cortis E; Muratori F; Lamioni A; Carsetti R; Cusano R; De Vito R; Perroni L; Gambarara M; Castro M; Bottazzo GF; Ugazio AG
Clin Gastroenterol Hepatol; 2006 May; 4(5):653-9. PubMed ID: 16630773
[TBL] [Abstract][Full Text] [Related]
10. A Case Report of IPEX Syndrome with Neonatal Diabetes Mellitus and Congenital Hypothyroidism as the Initial Presentation, and a Systematic Review of neonatal IPEX.
Hou AN; Wang Y; Pan YQ
J Clin Immunol; 2023 Jul; 43(5):979-988. PubMed ID: 36867340
[TBL] [Abstract][Full Text] [Related]
11. Immune reconstitution and recovery of FOXP3 (forkhead box P3)-expressing T cells after transplantation for IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome.
Zhan H; Sinclair J; Adams S; Cale CM; Murch S; Perroni L; Davies G; Amrolia P; Qasim W
Pediatrics; 2008 Apr; 121(4):e998-1002. PubMed ID: 18316354
[TBL] [Abstract][Full Text] [Related]
12. Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
Halabi-Tawil M; Ruemmele FM; Fraitag S; Rieux-Laucat F; Neven B; Brousse N; De Prost Y; Fischer A; Goulet O; Bodemer C
Br J Dermatol; 2009 Mar; 160(3):645-51. PubMed ID: 18795917
[TBL] [Abstract][Full Text] [Related]
13. Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder.
Sheikine Y; Woda CB; Lee PY; Chatila TA; Keles S; Charbonnier LM; Schmidt B; Rosen S; Rodig NM
Pediatr Nephrol; 2015 Jul; 30(7):1197-202. PubMed ID: 25911531
[TBL] [Abstract][Full Text] [Related]
14. Clinical, Immunological, and Genetic Features in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like Syndrome.
Jamee M; Zaki-Dizaji M; Lo B; Abolhassani H; Aghamahdi F; Mosavian M; Nademi Z; Mohammadi H; Jadidi-Niaragh F; Rojas M; Anaya JM; Azizi G
J Allergy Clin Immunol Pract; 2020 Sep; 8(8):2747-2760.e7. PubMed ID: 32428713
[TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular characteristics of immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China.
An YF; Xu F; Wang M; Zhang ZY; Zhao XD
Scand J Immunol; 2011 Sep; 74(3):304-309. PubMed ID: 21595732
[TBL] [Abstract][Full Text] [Related]
16. Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene.
Torgerson TR; Linane A; Moes N; Anover S; Mateo V; Rieux-Laucat F; Hermine O; Vijay S; Gambineri E; Cerf-Bensussan N; Fischer A; Ochs HD; Goulet O; Ruemmele FM
Gastroenterology; 2007 May; 132(5):1705-17. PubMed ID: 17484868
[TBL] [Abstract][Full Text] [Related]
17. 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
J Clin Res Pediatr Endocrinol; 2022 Aug; 14(3):361-365. PubMed ID: 34044499
[TBL] [Abstract][Full Text] [Related]
18. Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.
Colobran R; Álvarez de la Campa E; Soler-Palacín P; Martín-Nalda A; Pujol-Borrell R; de la Cruz X; Martínez-Gallo M
Clin Immunol; 2016 Feb; 163():60-5. PubMed ID: 26748374
[TBL] [Abstract][Full Text] [Related]
19. IPEX and the role of Foxp3 in the development and function of human Tregs.
Le Bras S; Geha RS
J Clin Invest; 2006 Jun; 116(6):1473-5. PubMed ID: 16741571
[TBL] [Abstract][Full Text] [Related]
20. IPEX as a result of mutations in FOXP3.
van der Vliet HJ; Nieuwenhuis EE
Clin Dev Immunol; 2007; 2007():89017. PubMed ID: 18317533
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]