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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
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] Page: [Next] [New Search]