BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 18931102)

  • 1. Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.
    Rubio-Cabezas O; Minton JA; Caswell R; Shield JP; Deiss D; Sumnik Z; Cayssials A; Herr M; Loew A; Lewis V; Ellard S; Hattersley AT
    Diabetes Care; 2009 Jan; 32(1):111-6. PubMed ID: 18931102
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
    Hwang JL; Park SY; Ye H; Sanyoura M; Pastore AN; Carmody D; Del Gaudio D; Wilson JF; Hanis CL; Liu X; Atzmon G; Glaser B; Philipson LH; Greeley SAW;
    Pediatr Diabetes; 2018 May; 19(3):388-392. PubMed ID: 29193502
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in two cases].
    Zhu Q; Yuan K; Wang C; Fang Y; Zhu J; Liang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):389-392. PubMed ID: 29896738
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [New mutation in FOXP3 gene identified in an infant with chronic diarrhea as manifestation of autoinmune enteropathy - IPEX syndrome].
    Plata García C; Martín-Marín L; Soler-Ramírez A; Rojas JA; Salazar MP
    Rev Chil Pediatr; 2020 Aug; 91(4):584-590. PubMed ID: 33399737
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX).
    Kobayashi I; Shiari R; Yamada M; Kawamura N; Okano M; Yara A; Iguchi A; Ishikawa N; Ariga T; Sakiyama Y; Ochs HD; Kobayashi K
    J Med Genet; 2001 Dec; 38(12):874-6. PubMed ID: 11768393
    [No Abstract]   [Full Text] [Related]  

  • 11. IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T
    Magg T; Wiebking V; Conca R; Krebs S; Arens S; Schmid I; Klein C; Albert MH; Hauck F
    Clin Immunol; 2018 Jun; 191():52-58. PubMed ID: 29567430
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. IPEX Syndrome: Genetics and Treatment Options.
    Ben-Skowronek I
    Genes (Basel); 2021 Feb; 12(3):. PubMed ID: 33668198
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [From Ipex to foxp3: a new contribution of pediatrics to the understanding of the immune system].
    Marabelle A; Meyer M; Demeocq F; Lachaux A
    Arch Pediatr; 2008 Jan; 15(1):55-63. PubMed ID: 18155891
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child].
    An YF; Zhao XD; Xu F; Yang XQ
    Zhonghua Er Ke Za Zhi; 2009 Nov; 47(11):824-8. PubMed ID: 20078992
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unusual and early onset IPEX syndrome: a case report.
    Doğruel D; Gürbüz F; Turan İ; Altıntaş DU; Yılmaz M; Yüksel B
    Turk J Pediatr; 2019; 61(4):580-584. PubMed ID: 31990476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of Metaplastic atrophic gastritis in immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) syndrome.
    Luo Y; Chen J; Fang Y; Lou J; Yu J
    BMC Pediatr; 2018 Jun; 18(1):191. PubMed ID: 29907148
    [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. FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome.
    Wyatt RC; Olek S; De Franco E; Samans B; Patel K; Houghton J; Walter S; Schulze J; Bacchetta R; Hattersley AT; Flanagan SE; Johnson MB
    J Clin Immunol; 2023 Apr; 43(3):662-669. PubMed ID: 36600150
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical features and genetic analysis of three patients with Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome due to variants of FOXP3 gene].
    Zheng C; Meng Y; Deng Z; Liu J; Yan G; Huang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Feb; 41(2):181-186. PubMed ID: 38311556
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.