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Journal Abstract Search


221 related items for PubMed ID: 23428118

  • 1. [Association of tumor necrosis factor-alpha gene polymorphisms with Henoch-Schonlein purpura nephritis in children].
    Wang JJ, Shi YP, Huang Y, Wu C, Li XC.
    Zhongguo Dang Dai Er Ke Za Zhi; 2013 Feb; 15(2):88-90. PubMed ID: 23428118
    [Abstract] [Full Text] [Related]

  • 2. Gene polymorphism of vascular endothelial growth factor in children with Henoch-Schonlein purpura nephritis.
    Zeng HS, Xiong XY, Chen YY, Luo XP.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jun; 11(6):417-21. PubMed ID: 19558800
    [Abstract] [Full Text] [Related]

  • 3. Role of PAX2 gene polymorphisms in Henoch-Schonlein purpura nephritis.
    Yi ZW, Fang XL, Wu XC, He XJ, He QN, Dang XQ, Zhu CP, Mo SH.
    Nephrology (Carlton); 2006 Feb; 11(1):42-8. PubMed ID: 16509931
    [Abstract] [Full Text] [Related]

  • 4. Association of endothelial nitric oxide synthase gene polymorphism with the risk of Henoch-Schönlein purpura/Henoch-Schönlein purpura nephritis.
    Zhong W, Zhou TB, Jiang Z.
    Ren Fail; 2015 Apr; 37(3):372-6. PubMed ID: 25585947
    [Abstract] [Full Text] [Related]

  • 5. Heat shock protein 70-2 and tumor necrosis factor-α gene polymorphisms in Chinese children with Henoch-Schönlein purpura.
    Ding GX, Wang CH, Che RC, Guan WZ, Yuan YG, Su M, Zhang AH, Huang SM.
    World J Pediatr; 2016 Feb; 12(1):49-54. PubMed ID: 26547206
    [Abstract] [Full Text] [Related]

  • 6. Association of Endothelial Nitric Oxide Synthase Gene Polymorphism with Susceptibility and Nephritis Development of Henoch-Schönlein Purpura in Chinese Han Children.
    Wang A, Wang A, Xiao Y, Wang J, Xu E.
    Genet Test Mol Biomarkers; 2017 Jun; 21(6):373-381. PubMed ID: 28409662
    [Abstract] [Full Text] [Related]

  • 7. [Clinical significance of serum levels of IGF-1 and IGFBP-3 in children with Henoch-Schonlein purpura or Henoch-Schonlein purpura nephritis].
    Ru L, Abudouhaer A, Guo YF.
    Zhongguo Dang Dai Er Ke Za Zhi; 2013 Nov; 15(11):1009-13. PubMed ID: 24229600
    [Abstract] [Full Text] [Related]

  • 8. Association between functional haplotypes of vascular endothelial growth factor and renal complications in Henoch-Schönlein purpura.
    Rueda B, Perez-Armengol C, Lopez-Lopez S, Garcia-Porrua C, Martín J, Gonzalez-Gay MA.
    J Rheumatol; 2006 Jan; 33(1):69-73. PubMed ID: 16395752
    [Abstract] [Full Text] [Related]

  • 9. Effect of paraoxonase 1 gene polymorphisms on clinical course of Henoch-Schönlein purpura.
    Yilmaz A, Emre S, Agachan B, Bilge I, Yilmaz H, Ergen A, Isbir T, Sirin A.
    J Nephrol; 2009 Jan; 22(6):726-32. PubMed ID: 19967651
    [Abstract] [Full Text] [Related]

  • 10. [Meta-analysis of the association between angiotension-converting enzyme I/D polymorphism and susceptibility to children with Henoch-Schönlein purpura or Henoch-Schölein purpura nephritis].
    Li H, Zhao D, Yang Q.
    Zhonghua Yi Xue Za Zhi; 2014 Jul 08; 94(26):2039-44. PubMed ID: 25312666
    [Abstract] [Full Text] [Related]

  • 11. [Association between CTLA-4 gene polymorphism and Henoch-Schönlein purpura in children].
    Hou HH, Huang YP, Liu L, He GT.
    Zhongguo Dang Dai Er Ke Za Zhi; 2017 Mar 08; 19(3):296-302. PubMed ID: 28302200
    [Abstract] [Full Text] [Related]

  • 12. [Roles of serum and urinary interleukins 13Ralpha2 and other cytokines in pediatric Henoch-Schonlein purpura].
    Yu YH, Pan KL, Li Q, Zhang BJ, Huang Y, Zhang JJ, DU L.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jan 08; 11(1):37-40. PubMed ID: 19149920
    [Abstract] [Full Text] [Related]

  • 13. Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients.
    Nalbantoglu S, Tabel Y, Mir S, Berdeli A.
    Cytokine; 2013 Apr 08; 62(1):160-4. PubMed ID: 23523092
    [Abstract] [Full Text] [Related]

  • 14. [Clinical Significance of Serum Midkine in Children with Henoch-Schonlein Purpura].
    Li MM, Liu N, Zhagn M, Xue HR.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Feb 08; 25(1):181-185. PubMed ID: 28245398
    [Abstract] [Full Text] [Related]

  • 15. C1GALT1 polymorphisms are associated with Henoch-Schönlein purpura nephritis.
    He X, Zhao P, Kang S, Ding Y, Luan J, Liu Z, Wu Y, Yin W.
    Pediatr Nephrol; 2012 Sep 08; 27(9):1505-9. PubMed ID: 22544166
    [Abstract] [Full Text] [Related]

  • 16. No evidence of association between functional polymorphisms located within IL6R and IL6ST genes and Henoch-Schönlein purpura.
    López-Mejías R, Sevilla Pérez B, Genre F, Castañeda S, Ortego-Centeno N, Llorca J, Ubilla B, Ochoa R, Pina T, Marquez A, Sala-Icardo L, Miranda-Filloy JA, Rueda-Gotor J, Martín J, Blanco R, González-Gay MA.
    Tissue Antigens; 2013 Dec 08; 82(6):416-9. PubMed ID: 24498998
    [Abstract] [Full Text] [Related]

  • 17. Lack of association between endothelial nitric oxide synthase polymorphisms and Henoch-Schönlein purpura.
    Amoli MM, Garcia-Porrua C, Calviño MC, Ollier WE, Gonzalez-Gay MA.
    J Rheumatol; 2004 Feb 08; 31(2):299-301. PubMed ID: 14760800
    [Abstract] [Full Text] [Related]

  • 18. Association study between matrix metalloproteinase-9 gene (MMP9) polymorphisms and the risk of Henoch-Schönlein purpura in children.
    Xu ED, Xiao YF, Wang JJ, Dong L.
    Genet Mol Res; 2016 Jun 03; 15(2):. PubMed ID: 27323137
    [Abstract] [Full Text] [Related]

  • 19. Serum levels of alpha-smooth muscle actin and c-Met as biomarkers of the degree of severity of Henoch-Schonlein purpura nephritis.
    Zhang L, Han C, Sun C, Meng H, Ye F, Na S, Chen F, Zhang D, Jin X.
    Transl Res; 2013 Jan 03; 161(1):26-36. PubMed ID: 23041443
    [Abstract] [Full Text] [Related]

  • 20. Inducible nitric oxide synthase polymorphism is associated with susceptibility to Henoch-Schönlein purpura in northwestern Spain.
    Martin J, Paco L, Ruiz MP, Lopez-Nevot MA, Garcia-Porrua C, Amoli MM, Calviño MC, Ollier WE, Gonzalez-Gay MA.
    J Rheumatol; 2005 Jun 03; 32(6):1081-5. PubMed ID: 15940772
    [Abstract] [Full Text] [Related]


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