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143 related items for PubMed ID: 31889944

  • 1. Neonatal Crohn's disease with Oral ulcer as the first symptom caused by a compound heterozygote mutation in IL-10RA: a case report.
    Lv H, Qiao B, Fang L, Yang L, Wang Q, Wu S, Ren P, Li L.
    Hereditas; 2019; 156():38. PubMed ID: 31889944
    [Abstract] [Full Text] [Related]

  • 2. Interleukin-10 receptor mutations in children with neonatal-onset Crohn's disease and intractable ulcerating enterocolitis.
    Shim JO, Hwang S, Yang HR, Moon JS, Chang JY, Ko JS, Park SS, Kang GH, Kim WS, Seo JK.
    Eur J Gastroenterol Hepatol; 2013 Oct; 25(10):1235-40. PubMed ID: 23839161
    [Abstract] [Full Text] [Related]

  • 3. [Interleukin-10 receptor mutations in children with neonatal onset inflammatory bowel disease: genetic diagnosis and pathogenesis].
    Lu D, Xu Y, Chen Y, Zeng P, Chen H, Zeng H.
    Zhonghua Er Ke Za Zhi; 2015 May; 53(5):348-54. PubMed ID: 26080664
    [Abstract] [Full Text] [Related]

  • 4. Novel de novo mutations of the interleukin-10 receptor gene lead to infantile onset inflammatory bowel disease.
    Lee CH, Hsu P, Nanan B, Nanan R, Wong M, Gaskin KJ, Leong RW, Murchie R, Muise AM, Stormon MO.
    J Crohns Colitis; 2014 Nov; 8(11):1551-6. PubMed ID: 24813381
    [Abstract] [Full Text] [Related]

  • 5. [Interleukin-10 receptor gene mutations induced very early onset inflammatory bowel disease in 6 infants].
    Wang FP, Ma X, Zhu D, Gong YZ, Ning HJ, Zhong XM.
    Zhonghua Er Ke Za Zhi; 2018 Oct 02; 56(10):753-758. PubMed ID: 30293279
    [Abstract] [Full Text] [Related]

  • 6. Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease.
    Xiao Y, Wang XQ, Yu Y, Guo Y, Xu X, Gong L, Zhou T, Li XQ, Xu CD.
    World J Gastroenterol; 2016 Jun 28; 22(24):5578-88. PubMed ID: 27350736
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  • 8. Very early-onset inflammatory bowel disease (IBD) in infancy is a different disease entity from adult-onset IBD; one form of interleukin-10 receptor mutations.
    Shim JO, Seo JK.
    J Hum Genet; 2014 Jun 28; 59(6):337-41. PubMed ID: 24785691
    [Abstract] [Full Text] [Related]

  • 9. Novel Compound Heterozygote Mutation in IL10RA in a Patient With Very Early-Onset Inflammatory Bowel Disease.
    Oh SH, Sung YH, Kim I, Sim CK, Lee JH, Baek M, Pack CG, Seok C, Seo EJ, Lee MS, Kim KM.
    Inflamm Bowel Dis; 2019 Feb 21; 25(3):498-509. PubMed ID: 30462267
    [Abstract] [Full Text] [Related]

  • 10. Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease.
    Mao H, Yang W, Lee PP, Ho MH, Yang J, Zeng S, Chong CY, Lee TL, Tu W, Lau YL.
    Genes Immun; 2012 Jul 21; 13(5):437-42. PubMed ID: 22476154
    [Abstract] [Full Text] [Related]

  • 11. Importance of early detection of infantile inflammatory bowel disease with defective IL-10 pathway: A case report.
    Hung HH, Lee HC, Yeung CY, Wang NL, Tang TY, Winter HS, Kelsen JR, Jiang CB.
    Medicine (Baltimore); 2021 May 28; 100(21):e25868. PubMed ID: 34032699
    [Abstract] [Full Text] [Related]

  • 12. IL-10RA Mutation as a Risk Factor of Severe Influenza-Associated Encephalopathy: A Case Report.
    Ishige T, Igarashi Y, Hatori R, Tatsuki M, Sasahara Y, Takizawa T, Arakawa H.
    Pediatrics; 2018 Jun 28; 141(6):. PubMed ID: 29724880
    [Abstract] [Full Text] [Related]

  • 13. Elevated IgA and IL-10 levels in very-early-onset inflammatory bowel disease secondary to IL-10 receptor deficiency.
    Sandy NS, Marega LF, Bechara GD, Riccetto AGL, Bonfim C, Vilela MMDS, Ribeiro AF, Servidoni MF, Lomazi EA.
    Rev Paul Pediatr; 2021 Jun 28; 40():e2020434. PubMed ID: 34730757
    [Abstract] [Full Text] [Related]

  • 14. Genetic association and epistatic interaction of the interleukin-10 signaling pathway in pediatric inflammatory bowel disease.
    Lin Z, Wang Z, Hegarty JP, Lin TR, Wang Y, Deiling S, Wu R, Thomas NJ, Floros J.
    World J Gastroenterol; 2017 Jul 21; 23(27):4897-4909. PubMed ID: 28785144
    [Abstract] [Full Text] [Related]

  • 15. IL-10R polymorphisms are associated with very-early-onset ulcerative colitis.
    Moran CJ, Walters TD, Guo CH, Kugathasan S, Klein C, Turner D, Wolters VM, Bandsma RH, Mouzaki M, Zachos M, Langer JC, Cutz E, Benseler SM, Roifman CM, Silverberg MS, Griffiths AM, Snapper SB, Muise AM.
    Inflamm Bowel Dis; 2013 Jan 21; 19(1):115-23. PubMed ID: 22550014
    [Abstract] [Full Text] [Related]

  • 16. [Clinical and genotypic characteristics of infantile inflammatory bowel disease].
    Gong YZ, Ning HJ, Ma X, Zhu D, Wang FP, Zhang R, Zhang YL, Zhong XM.
    Zhonghua Er Ke Za Zhi; 2019 Jul 02; 57(7):520-525. PubMed ID: 31269551
    [Abstract] [Full Text] [Related]

  • 17. Mutations in Interleukin-10 Receptor and Clinical Phenotypes in Patients with Very Early Onset Inflammatory Bowel Disease: A Chinese VEO-IBD Collaboration Group Survey.
    Huang Z, Peng K, Li X, Zhao R, You J, Cheng X, Wang Z, Wang Y, Wu B, Wang H, Zeng H, Yu Z, Zheng C, Wang Y, Huang Y.
    Inflamm Bowel Dis; 2017 Apr 02; 23(4):578-590. PubMed ID: 28267044
    [Abstract] [Full Text] [Related]

  • 18. Very early onset inflammatory bowel disease: Investigation of the IL-10 signaling pathway in Iranian children.
    Nemati S, Teimourian S, Tabrizi M, Najafi M, Dara N, Imanzadeh F, Ahmadi M, Aghdam MK, Tavassoli M, Rohani P, Madani SR, de Boer M, Kuijpers TW, Roos D.
    Eur J Med Genet; 2017 Dec 02; 60(12):643-649. PubMed ID: 28864178
    [Abstract] [Full Text] [Related]

  • 19. Clinical features of interleukin 10 receptor gene mutations in children with very early-onset inflammatory bowel disease.
    Beser OF, Conde CD, Serwas NK, Cokugras FC, Kutlu T, Boztug K, Erkan T.
    J Pediatr Gastroenterol Nutr; 2015 Mar 02; 60(3):332-8. PubMed ID: 25373860
    [Abstract] [Full Text] [Related]

  • 20. TLR4, IL10RA, and NOD2 mutation in paediatric Crohn's disease patients: an association with Mycobacterium avium subspecies paratuberculosis and TLR4 and IL10RA expression.
    Wagner J, Skinner NA, Catto-Smith AG, Cameron DJ, Michalski WP, Visvanathan K, Kirkwood CD.
    Med Microbiol Immunol; 2013 Aug 02; 202(4):267-76. PubMed ID: 23455702
    [Abstract] [Full Text] [Related]

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