177 related articles for article (PubMed ID: 28963667)
41. 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]
42. HLA-DRB1 in Henoch-Schönlein purpura: A susceptibility study from North India.
Aggarwal R; Gupta A; Naru J; Berka N; Nanda N; Suri D; Singh S
Hum Immunol; 2016 Jul; 77(7):555-8. PubMed ID: 27184863
[TBL] [Abstract][Full Text] [Related]
43. A study on the association between C1GALT1 polymorphisms and the risk of Henoch-Schönlein purpura in a Chinese population.
An J; Lü Q; Zhao H; Cao Y; Yan B; Ma Z
Rheumatol Int; 2013 Oct; 33(10):2539-42. PubMed ID: 23624553
[TBL] [Abstract][Full Text] [Related]
44. Imbalance of interleukin-18 and interleukin-18 binding protein in children with Henoch-Schönlein purpura.
Wang YB; Shan NN; Chen O; Gao Y; Zou X; Wei DE; Wang CX; Zhang Y
J Int Med Res; 2011; 39(6):2201-8. PubMed ID: 22289535
[TBL] [Abstract][Full Text] [Related]
45. 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; 32(6):1081-5. PubMed ID: 15940772
[TBL] [Abstract][Full Text] [Related]
46. Clinical significance of the serum biomarker index detection in children with Henoch-Schonlein purpura.
Purevdorj N; Mu Y; Gu Y; Zheng F; Wang R; Yu J; Sun X
Clin Biochem; 2018 Feb; 52():167-170. PubMed ID: 29129626
[TBL] [Abstract][Full Text] [Related]
47. Association of HLA-B*41:02 with Henoch-Schönlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status.
López-Mejías R; Genre F; Pérez BS; Castañeda S; Ortego-Centeno N; Llorca J; Ubilla B; Remuzgo-Martínez S; Mijares V; Pina T; Calvo-Río V; Márquez A; Miranda-Filloy JA; Parejo AN; Conde-Jaldón M; Ortiz-Fernández L; Argila D; Aragües M; Rubio E; Luque ML; Blanco-Madrigal JM; Galíndez-Aguirregoikoa E; González Escribano F; Ocejo-Vinyals JG; Martín J; Blanco R; González-Gay MA
Arthritis Res Ther; 2015 Apr; 17(1):102. PubMed ID: 25889603
[TBL] [Abstract][Full Text] [Related]
48. The association between MEFV gene polymorphisms and Henoch-Schönlein purpura, and additional SNP-SNP interactions in Chinese Han children.
Xiong S; Xiong Y; Huang Q; Wang J; Zhang X
Rheumatol Int; 2017 Mar; 37(3):455-460. PubMed ID: 27796522
[TBL] [Abstract][Full Text] [Related]
49. Interferon-gamma gene polymorphism +874 (a/t) in Chinese children with Henoch-Schonlein purpura.
Xu H; Li W; Fu H; Jiang G
Iran J Allergy Asthma Immunol; 2014 Jun; 13(3):184-9. PubMed ID: 24659122
[TBL] [Abstract][Full Text] [Related]
50. Expansion of Circulating T Follicular Helper Cells in Children with Acute Henoch-Schönlein Purpura.
Xie J; Liu Y; Wang L; Ruan G; Yuan H; Fang H; Wu J; Cui D
J Immunol Res; 2015; 2015():742535. PubMed ID: 26491701
[TBL] [Abstract][Full Text] [Related]
51. 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
[TBL] [Abstract][Full Text] [Related]
52. Henoch-Schonlein purpura: polymorphisms in thrombophilia genes.
Dagan E; Brik R; Broza Y; Gershoni-Baruch R
Pediatr Nephrol; 2006 Aug; 21(8):1117-21. PubMed ID: 16791607
[TBL] [Abstract][Full Text] [Related]
53. Prevalence of MEFV gene mutations and their clinical correlations in Turkish children with Henoch-Schönlein purpura.
Bayram C; Demircin G; Erdoğan O; Bülbül M; Caltik A; Akyüz SG
Acta Paediatr; 2011 May; 100(5):745-9. PubMed ID: 21231959
[TBL] [Abstract][Full Text] [Related]
54. Increased frequency of C4B*Q0 alleles in patients with Henoch-Schönlein purpura.
Stefansson Thors V; Kolka R; Sigurdardottir SL; Edvardsson VO; Arason G; Haraldsson A
Scand J Immunol; 2005 Mar; 61(3):274-8. PubMed ID: 15787745
[TBL] [Abstract][Full Text] [Related]
55. [Association of Cosmc gene mutation with susceptibility to Henoch-Schönlein purpura in children].
Xie QL; Mo X; Liu SL; Zhu MA; Tao Y; Zhang XQ; Wang J; Jin YL
Zhongguo Dang Dai Er Ke Za Zhi; 2016 Jul; 18(7):625-9. PubMed ID: 27412546
[TBL] [Abstract][Full Text] [Related]
56. The CD18 AvaII polymorphic site not associated with Henoch-Schönlein purpura.
He X; Li Y; Kang S; Luan J; Wu Y; Liu Z; Yin W
Clin Exp Rheumatol; 2011; 29(1 Suppl 64):S117-20. PubMed ID: 21269583
[TBL] [Abstract][Full Text] [Related]
57. HLA-B35 association with nephritis in Henoch-Schönlein purpura.
Amoli MM; Thomson W; Hajeer AH; Calviño MC; Garcia-Porrua C; Ollier WE; Gonzalez-Gay MA
J Rheumatol; 2002 May; 29(5):948-9. PubMed ID: 12022355
[TBL] [Abstract][Full Text] [Related]
58. 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
[TBL] [Abstract][Full Text] [Related]
59. Association of IL-10 gene polymorphisms and susceptibility to Juvenile Idiopathic Arthritis in Egyptian children and adolescents: a case-control study.
Fathy MM; Elsaadany HF; Ali YF; Farghaly MA; Hamed ME; Ibrahim HE; Noah MA; Allah MA; Elashkar SS; Abdelsalam NI; Abdelrahman HM; Ahmed AR; Anany HG; Ismail SM; Ibrahim BR; Al Azizi NM; Gawish HH; Al-Akad GM; Nabil RM; Fahmy DS; Alsayed SF
Ital J Pediatr; 2017 Jan; 43(1):9. PubMed ID: 28257625
[TBL] [Abstract][Full Text] [Related]
60. MicroRNA profiling in Chinese children with Henoch-Schonlein purpura and association between selected microRNAs and inflammatory biomarkers.
Li J; Chen M; Wang J; Lu L; Li X; Le Y
Acta Paediatr; 2021 Jul; 110(7):2221-2229. PubMed ID: 33533510
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
