233 related articles for article (PubMed ID: 28691415)
21. The genetics of Henoch-Schönlein purpura: a systematic review and meta-analysis.
He X; Yu C; Zhao P; Ding Y; Liang X; Zhao Y; Yue X; Wu Y; Yin W
Rheumatol Int; 2013 Jun; 33(6):1387-95. PubMed ID: 23325094
[TBL] [Abstract][Full Text] [Related]
22. Polymorphism at codon 469 of the intercellular adhesion molecule-1 locus is associated with protection against severe gastrointestinal complications in Henoch-Schönlein purpura.
Amoli MM; Mattey DL; Calviño MC; Garcia-Porrua C; Thomson W; Hajeer AH; Ollier WE; Gonzalez-Gay MA
J Rheumatol; 2001 May; 28(5):1014-8. PubMed ID: 11361181
[TBL] [Abstract][Full Text] [Related]
23. Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).
López-Mejías R; Genre F; Remuzgo-Martínez S; Pérez BS; Castañeda S; Llorca J; Ortego-Centeno N; Ubilla B; Mijares V; Pina T; Calvo-Río V; Palmou N; Miranda-Filloy JA; Parejo AN; Argila D; Sánchez-Pérez J; Rubio E; Luque ML; Blanco-Madrigal JM; Galíndez-Aguirregoikoa E; Ocejo-Vinyals JG; Martín J; Blanco R; González-Gay MA
Arthritis Res Ther; 2015 Oct; 17():286. PubMed ID: 26458874
[TBL] [Abstract][Full Text] [Related]
24. [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; 19(3):296-302. PubMed ID: 28302200
[TBL] [Abstract][Full Text] [Related]
25. [The I/D polymorphism of the ACE gene in children with Henoch-Schoenlein purpura].
Brodkiewicz A; Ciechanowicz A; Urbańska A; Peregud-Pogorzelski J; Dzieński P; Subicka D; Fydryk J
Pol Merkur Lekarski; 2000 Apr; 8(46):236-8. PubMed ID: 10897627
[TBL] [Abstract][Full Text] [Related]
26. CTLA-4 exon 1 +49A/G polymorphism is associated with renal involvement in pediatric Henoch-Schönlein purpura.
Wang JJ; Shi YP; Yue H; Chun W; Zou LP
Pediatr Nephrol; 2012 Nov; 27(11):2059-2064. PubMed ID: 22700162
[TBL] [Abstract][Full Text] [Related]
27. [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
[TBL] [Abstract][Full Text] [Related]
28. Association between HLA-A and -B polymorphisms and susceptibility to Henoch-Schönlein purpura in Han and Mongolian children from Inner Mongolia.
Ren SM; Yang GL; Liu CZ; Zhang CX; Shou QH; Yu SF; Li WC; Su XL
Genet Mol Res; 2012 Feb; 11(1):221-8. PubMed ID: 22370889
[TBL] [Abstract][Full Text] [Related]
29. Inducible nitric oxide synthase gene polymorphisms are associated with a risk of nephritis in Henoch-Schönlein purpura children.
Jiang J; Duan W; Shang X; Wang H; Gao Y; Tian P; Zhou Q
Eur J Pediatr; 2017 Aug; 176(8):1035-1045. PubMed ID: 28593405
[TBL] [Abstract][Full Text] [Related]
30. 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; 31(2):299-301. PubMed ID: 14760800
[TBL] [Abstract][Full Text] [Related]
31. Interleukin 1 beta (IL1ß) rs16944 genetic variant as a genetic marker of severe renal manifestations and renal sequelae in Henoch-Schönlein purpura.
López-Mejías R; Genre F; Remuzgo-Martínez S; Sevilla Pérez B; Castañeda S; Llorca J; Ortego-Centeno N; Ubilla B; Mijares V; Pina T; Calvo-Río V; Miranda-Filloy JA; Navas Parejo A; Argila D; Sánchez-Pérez J; Rubio E; Luque ML; Blanco-Madrigal JM; Galíndez-Aguirregoikoa E; Martín J; Blanco R; González-Gay MA
Clin Exp Rheumatol; 2016; 34(3 Suppl 97):S84-8. PubMed ID: 26842496
[TBL] [Abstract][Full Text] [Related]
32. 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; 22(6):726-32. PubMed ID: 19967651
[TBL] [Abstract][Full Text] [Related]
33. Association of the paired box 2 gene polymorphism with the susceptibility and pathogenesis of Henoch‑Schönlein purpura in children.
Chen J; Fang X; Dang X; Wu X; Yi Z
Mol Med Rep; 2015 Mar; 11(3):1997-2003. PubMed ID: 25385517
[TBL] [Abstract][Full Text] [Related]
34. HLA class 1 associations in Henoch Schonlein purpura: increased and decreased frequencies.
Peru H; Soylemezoglu O; Gonen S; Cetinyurek A; Bakkaloğlu SA; Buyan N; Hasanoglu E
Clin Rheumatol; 2008 Jan; 27(1):5-10. PubMed ID: 17487448
[TBL] [Abstract][Full Text] [Related]
35. Methylenetetrahydrofolate reductase C677T polymorphism in patients with Henoch-Schönlein purpura.
Emre S; Sirin A; Ergen A; Bilge I; Sucu A; Yilmaz A; Isbir T
Pediatr Int; 2011 Jun; 53(3):358-62. PubMed ID: 20831652
[TBL] [Abstract][Full Text] [Related]
36. Lack of association between interleukin-6 promoter polymorphism at position -174 and Henoch-Schönlein pur pura.
Amoli MM; Martin J; Miranda-Filloy JA; Garcia-Porrua C; Ollier WE; Gonzalez-Gay MA
Clin Exp Rheumatol; 2007; 25(1 Suppl 44):S6-9. PubMed ID: 17428355
[TBL] [Abstract][Full Text] [Related]
37. 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; 27(9):1505-9. PubMed ID: 22544166
[TBL] [Abstract][Full Text] [Related]
38. CTLA-4 +49 A/G genotype and HLA-DRB1 polymorphisms in Turkish patients with Henoch-Schönlein purpura.
Soylemezoglu O; Peru H; Gonen S; Cetinyurek A; Ozkaya O; Bakkaloğlu S; Buyan N; Hasanoglu E
Pediatr Nephrol; 2008 Aug; 23(8):1239-44. PubMed ID: 18449568
[TBL] [Abstract][Full Text] [Related]
39. HLA-DRB1 alleles and Henoch-Schönlein purpura: susceptibility and severity of disease.
Soylemezoglu O; Peru H; Gonen S; Cetinyurek A; Buyan N
J Rheumatol; 2008 Jun; 35(6):1165-8. PubMed ID: 18412308
[TBL] [Abstract][Full Text] [Related]
40. 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; 15(2):. PubMed ID: 27323137
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]