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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 16091915)

  • 1. Low-dose cyclosporine A in a patient with X-linked immune dysregulation, polyendocrinopathy and enteropathy.
    Tanaka H; Tsugawa K; Kudo M; Sugimoto K; Kobayashi I; Ito E
    Eur J Pediatr; 2005 Dec; 164(12):779-80. PubMed ID: 16091915
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
    Hashimura Y; Nozu K; Kanegane H; Miyawaki T; Hayakawa A; Yoshikawa N; Nakanishi K; Takemoto M; Iijima K; Matsuo M
    Pediatr Nephrol; 2009 Jun; 24(6):1181-6. PubMed ID: 19189134
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.
    Harbuz R; Lespinasse J; Boulet S; Francannet C; Creveaux I; Benkhelifa M; Jouk PS; Lunardi J; Ray PF
    Prenat Diagn; 2010 Nov; 30(11):1072-8. PubMed ID: 20842625
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndrome.
    Passerini L; Di Nunzio S; Gregori S; Gambineri E; Cecconi M; Seidel MG; Cazzola G; Perroni L; Tommasini A; Vignola S; Guidi L; Roncarolo MG; Bacchetta R
    Eur J Immunol; 2011 Apr; 41(4):1120-31. PubMed ID: 21400500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study.
    Duclaux-Loras R; Charbit-Henrion F; Neven B; Nowak J; Collardeau-Frachon S; Malcus C; Ray PF; Moshous D; Beltrand J; Goulet O; Cerf-Bensussan N; Lachaux A; Rieux-Laucat F; Ruemmele FM
    Clin Transl Gastroenterol; 2018 Nov; 9(10):201. PubMed ID: 30385752
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
    Otsubo K; Kanegane H; Kamachi Y; Kobayashi I; Tsuge I; Imaizumi M; Sasahara Y; Hayakawa A; Nozu K; Iijima K; Ito S; Horikawa R; Nagai Y; Takatsu K; Mori H; Ochs HD; Miyawaki T
    Clin Immunol; 2011 Oct; 141(1):111-20. PubMed ID: 21802372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells.
    Torgerson TR; Ochs HD
    J Allergy Clin Immunol; 2007 Oct; 120(4):744-50; quiz 751-2. PubMed ID: 17931557
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Late-onset of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome (IPEX) with intractable diarrhea.
    Zama D; Cocchi I; Masetti R; Specchia F; Alvisi P; Gambineri E; Lima M; Pession A
    Ital J Pediatr; 2014 Oct; 40():68. PubMed ID: 25326164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome).
    Bindl L; Torgerson T; Perroni L; Youssef N; Ochs HD; Goulet O; Ruemmele FM
    J Pediatr; 2005 Aug; 147(2):256-9. PubMed ID: 16126062
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and molecular aspects of autoimmune enteropathy and immune dysregulation, polyendocrinopathy autoimmune enteropathy X-linked syndrome.
    Ruemmele FM; Moes N; de Serre NP; Rieux-Laucat F; Goulet O
    Curr Opin Gastroenterol; 2008 Nov; 24(6):742-8. PubMed ID: 19122524
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autoantibodies to villin occur frequently in IPEX, a severe immune dysregulation, syndrome caused by mutation of FOXP3.
    Kobayashi I; Kubota M; Yamada M; Tanaka H; Itoh S; Sasahara Y; Whitesell L; Ariga T
    Clin Immunol; 2011 Oct; 141(1):83-9. PubMed ID: 21741320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regulatory T-like cells: another variation on the theme of hypomorphic mutations?
    Notarangelo LD
    Clin Immunol; 2011 Dec; 141(3):242-3. PubMed ID: 21955568
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: a model of immune dysregulation.
    Torgerson TR; Ochs HD
    Curr Opin Allergy Clin Immunol; 2002 Dec; 2(6):481-7. PubMed ID: 14752330
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Immune dysregulation, polyendocrinopathy and enteropathy, X-linked (IPEX) syndrome due to a mutation in FOXP3, modified by a pathogenic variant in SON (SON DNA-binding protein).
    Kylat RI; Stanley K; Simon S; Erickson RP
    J Appl Genet; 2023 Feb; 64(1):141-144. PubMed ID: 36175752
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.