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Items: 1 to 20 of 121

1.

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;82(6):416-9. doi: 10.1111/tan.12251.

PMID:
24498998
2.

Lack of association of IL6R rs2228145 and IL6ST/gp130 rs2228044 gene polymorphisms with cardiovascular disease in patients with rheumatoid arthritis.

López-Mejías R, García-Bermúdez M, González-Juanatey C, Castañeda S, Miranda-Filloy JA, Gómez-Vaquero C, Fernández-Gutiérrez B, Balsa A, Pascual-Salcedo D, Blanco R, González-Álvaro I, Llorca J, Martín J, González-Gay MA.

Tissue Antigens. 2011 Dec;78(6):438-41. doi: 10.1111/j.1399-0039.2011.01774.x.

PMID:
21981268
3.

No evidence of association between functional polymorphisms located within IL6R and IL6ST genes and systemic sclerosis.

Cénit MC, Simeón CP, Fonollosa V, Espinosa G, Beltrán E, Sáez-Comet L, Vicente-Rabaneda E, García-Hernández FJ, Martínez-Estupiñán L, Rodríguez-Carballeira M, Hernández V, de la Peña PG, Fernández-Castro M, Narváez FJ, Pros A, Gallego M, Ríos-Fernández R, Camps MT, Fernández-Nebro A, Egurbide MV, Carreira P, González-Gay MA, Martín J; Spanish Scleroderma Group..

Tissue Antigens. 2012 Sep;80(3):254-8. doi: 10.1111/j.1399-0039.2012.01915.x.

PMID:
22742541
4.

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 13;17:286. doi: 10.1186/s13075-015-0796-x.

5.

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.

PMID:
11361181
6.

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;62(1):160-4. doi: 10.1016/j.cyto.2013.02.024.

PMID:
23523092
7.

Interleukin 8 gene polymorphism is associated with increased risk of nephritis in cutaneous vasculitis.

Amoli MM, Thomson W, Hajeer AH, Calviño MC, Garcia-Porrua C, Ollier WE, Gonzalez-Gay MA.

J Rheumatol. 2002 Nov;29(11):2367-70.

PMID:
12415593
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.

PMID:
16395752
9.

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.

PMID:
14760800
10.

Interleukin 1 receptor antagonist gene polymorphism is associated with severe renal involvement and renal sequelae in Henoch-Schönlein purpura.

Amoli MM, Thomson W, Hajeer AH, Calviño MC, Garcia-Porrua C, Ollier WE, Gonzalez-Gay MA.

J Rheumatol. 2002 Jul;29(7):1404-7.

PMID:
12136897
11.

Interleukin 1beta gene polymorphism association with severe renal manifestations and renal sequelae in Henoch-Schönlein purpura.

Amoli MM, Calviño MC, Garcia-Porrua C, Llorca J, Ollier WE, Gonzalez-Gay MA.

J Rheumatol. 2004 Feb;31(2):295-8.

PMID:
14760799
12.

[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. Chinese.

13.

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.

PMID:
15940772
14.

TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement.

Soylu A, Kizildağ S, Kavukçu S, Cingöz S, Türkmen M, Demir BK, Sakizli M.

Rheumatol Int. 2010 Mar;30(5):667-70. doi: 10.1007/s00296-009-1052-y.

PMID:
19597734
15.

Association between RAS gene polymorphisms (ACE I/D, AGT M235T) and Henoch-Schönlein purpura in a Turkish population.

Nalbantoglu S, Tabel Y, Mir S, Serdaroğlu E, Berdeli A.

Dis Markers. 2013;34(1):23-32. doi: 10.3233/DMA-2012-120946.

16.

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.

PMID:
12022355
17.

Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement.

Ozkaya O, Söylemezoğlu O, Gönen S, Misirlioğlu M, Tuncer S, Kalman S, Buyan N, Hasanoğlu E.

Clin Rheumatol. 2006 Nov;25(6):861-5.

PMID:
16521052
18.

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 Jan-Feb;25(1 Suppl 44):S6-9.

PMID:
17428355
19.

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. doi: 10.3109/0886022X.2014.1000802.

PMID:
25585947
20.

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):2059-64. doi: 10.1007/s00467-012-2216-7.

PMID:
22700162
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