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Journal Abstract Search

247 related items for PubMed ID: 10451958

  • 21. Frequent immune response to a melanocyte specific protein KU-MEL-1 in patients with Vogt-Koyanagi-Harada disease.
    Otani S, Sakurai T, Yamamoto K, Fujita T, Matsuzaki Y, Goto Y, Ando Y, Suzuki S, Usui M, Takeuchi M, Kawakami Y.
    Br J Ophthalmol; 2006 Jun; 90(6):773-7. PubMed ID: 16481377
    [Abstract] [Full Text] [Related]

  • 22. [Association of HLA-DQA1 and DQB1 alleles with Vogt-Koyanagi-Harada syndrome in Han Chinese population].
    Liu Q, Zhang M, Qiu C, Hu T.
    Zhonghua Yan Ke Za Zhi; 1999 May; 35(3):210-5. PubMed ID: 11835809
    [Abstract] [Full Text] [Related]

  • 23. Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population.
    Shu Q, Yang P, Hou S, Li F, Chen Y, Du L, Jiang Z.
    Hum Immunol; 2010 Oct; 71(10):988-91. PubMed ID: 20620187
    [Abstract] [Full Text] [Related]

  • 24. PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome.
    Meng Q, Liu X, Yang P, Hou S, Du L, Zhou H, Kijlstra A.
    Mol Vis; 2009 Oct; 15():386-92. PubMed ID: 19234630
    [Abstract] [Full Text] [Related]

  • 25. HLA-DR is strongly associated with Vogt-Koyanagi-Harada disease in Mexican Mestizo patients.
    Arellanes-García L, Bautista N, Mora P, Ortega-Larrocea G, Burguet A, Gorodezky C.
    Ocul Immunol Inflamm; 1998 Jun; 6(2):93-100. PubMed ID: 9689639
    [Abstract] [Full Text] [Related]

  • 26. In silico prediction of binding of putative antigenic peptides to HLA-DRB1 alleles in Vogt-Koyanagi-Harada disease.
    Prasad PS, Levinson RD.
    Clin Immunol; 2005 Aug; 116(2):143-8. PubMed ID: 15927531
    [Abstract] [Full Text] [Related]

  • 27. Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population.
    Jiang Z, Yang P, Hou S, Li F, Zhou H.
    Hum Immunol; 2010 Apr; 71(4):414-7. PubMed ID: 20116410
    [Abstract] [Full Text] [Related]

  • 28. HLA-DRB1*0405 is the predominant allele in Brazilian patients with Vogt-Koyanagi-Harada disease.
    Goldberg AC, Yamamoto JH, Chiarella JM, Marin ML, Sibinelli M, Neufeld R, Hirata CE, Olivalves E, Kalil J.
    Hum Immunol; 1998 Mar; 59(3):183-8. PubMed ID: 9548078
    [Abstract] [Full Text] [Related]

  • 29. Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population.
    Hou S, Yang P, Du L, Zhou H, Lin X, Liu X, Kijlstra A.
    Mol Vis; 2008 Mar; 14():2597-603. PubMed ID: 19122825
    [Abstract] [Full Text] [Related]

  • 30. Revised diagnostic criteria for vogt-koyanagi-harada disease: considerations on the different disease categories.
    da Silva FT, Damico FM, Marin ML, Goldberg AC, Hirata CE, Takiuti PH, Olivalves E, Yamamoto JH.
    Am J Ophthalmol; 2009 Feb; 147(2):339-345.e5. PubMed ID: 18992868
    [Abstract] [Full Text] [Related]

  • 31. Elevated serum osteopontin levels and genetic polymorphisms of osteopontin are associated with Vogt-Koyanagi-Harada disease.
    Chu M, Yang P, Hu R, Hou S, Li F, Chen Y, Kijlstra A.
    Invest Ophthalmol Vis Sci; 2011 Sep 09; 52(10):7084-9. PubMed ID: 21810982
    [Abstract] [Full Text] [Related]

  • 32. Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.
    Chen Y, Yang P, Li F, Hou S, Jiang Z, Shu Q, Kijlstra A.
    Curr Eye Res; 2012 Apr 09; 37(4):312-7. PubMed ID: 22440163
    [Abstract] [Full Text] [Related]

  • 33. Vogt-Koyanagi-Harada syndrome in patients of Vietnamese ancestry.
    Riddington L, Hall AJ, Tait B, Nicholson I, Varney M.
    Aust N Z J Ophthalmol; 1996 May 09; 24(2):147-9. PubMed ID: 9199747
    [Abstract] [Full Text] [Related]

  • 34. [Polymorphism of HLA-DQB1 alleles in Chinese Han patients with Vogt-Koyanagi-Harada syndrome].
    Min HY, Liu Y, Niu NF, Zhang MF, Zhu XL, Zhao JL.
    Zhonghua Yan Ke Za Zhi; 2007 Apr 09; 43(4):355-60. PubMed ID: 17605936
    [Abstract] [Full Text] [Related]

  • 35. Association between Vogt-Koyanagi-Harada syndrome and HLA-DR1 and -DR4 in Hispanic patients living in southern California.
    Weisz JM, Holland GN, Roer LN, Park MS, Yuge AJ, Moorthy RS, Forster DJ, Rao NA, Terasaki PI.
    Ophthalmology; 1995 Jul 09; 102(7):1012-5. PubMed ID: 9121744
    [Abstract] [Full Text] [Related]

  • 36. Relationship between HLA-DRB1 and DQ alleles and the genetic susceptibility to type 1 diabetes.
    Sang Y, Yan C, Zhu C, Ni G.
    Chin Med J (Engl); 2001 Apr 09; 114(4):407-9. PubMed ID: 11780465
    [Abstract] [Full Text] [Related]

  • 37. Leptin increases in Vogt-Koyanagi-Harada (VKH) disease and promotes cell proliferation and inflammatory cytokine secretion.
    Liu L, Yang P, He H, Lin X, Jiang L, Chi W, Zhao C, Zhou H.
    Br J Ophthalmol; 2008 Apr 09; 92(4):557-61. PubMed ID: 18245271
    [Abstract] [Full Text] [Related]

  • 38. Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients.
    Horie Y, Takemoto Y, Miyazaki A, Namba K, Kase S, Yoshida K, Ota M, Hasumi Y, Inoko H, Mizuki N, Ohno S.
    Mol Vis; 2006 Dec 20; 12():1601-5. PubMed ID: 17200659
    [Abstract] [Full Text] [Related]

  • 39. [Relationship between human leukocyte antigen-DRB1 allele gene polymorphism and intrahepatic cholestasis of pregnancy].
    Chen F, Fan L, Xu L, Yao F.
    Zhonghua Fu Chan Ke Za Zhi; 2002 Sep 20; 37(9):519-22. PubMed ID: 12411009
    [Abstract] [Full Text] [Related]

  • 40. Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.
    Zheng M, Yu H, Zhang L, Li H, Liu Y, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2015 Dec 20; 56(13):8280-7. PubMed ID: 26747760
    [Abstract] [Full Text] [Related]

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