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PUBMED FOR HANDHELDS

Journal Abstract Search


280 related items for PubMed ID: 15607211

  • 21.
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  • 22. HLA-DRB1*1501, -DQB1*0301, -DQB1*0302, -DQB1*0602, and -DQB1*0603 alleles are associated with more severe disease outcome on MRI in patients with multiple sclerosis.
    Zivadinov R, Uxa L, Bratina A, Bosco A, Srinivasaraghavan B, Minagar A, Ukmar M, Benedetto Sy, Zorzon M.
    Int Rev Neurobiol; 2007; 79():521-35. PubMed ID: 17531857
    [Abstract] [Full Text] [Related]

  • 23. An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians.
    Bugeja MJ, Booth D, Bennetts B, Heard R, Rubio J, Stewart G.
    BMC Med Genet; 2006 Jul 26; 7():64. PubMed ID: 16872505
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  • 24.
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  • 25. [Multiple sclerosis--a disease with complex genetics].
    Myhr KM, Harbo HF.
    Tidsskr Nor Laegeforen; 2003 Oct 09; 123(19):2723-6. PubMed ID: 14600746
    [Abstract] [Full Text] [Related]

  • 26. CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population.
    Wray BN, Stankovich J, Whittock L, Dwyer T, Ponsonby AL, van der Mei IA, Taylor B, Dickinson J, Foote S, McMorran BJ.
    J Neuroimmunol; 2008 May 30; 196(1-2):139-42. PubMed ID: 18378005
    [Abstract] [Full Text] [Related]

  • 27. Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis.
    Galimberti D, Scalabrini D, Fenoglio C, De Riz M, Comi C, Venturelli E, Cortini F, Piola M, Leone M, Dianzani U, D'Alfonso S, Monaco F, Bresolin N, Scarpini E.
    J Neurol Sci; 2008 Apr 15; 267(1-2):86-90. PubMed ID: 17967467
    [Abstract] [Full Text] [Related]

  • 28. Genetics of multiple sclerosis.
    Fukazawa T, Sasaki H, Kikuchi S, Hamada T, Tashiro K.
    Biomed Pharmacother; 2000 Mar 15; 54(2):103-6. PubMed ID: 10759295
    [Abstract] [Full Text] [Related]

  • 29. Association to the Glypican-5 gene in multiple sclerosis.
    Lorentzen AR, Melum E, Ellinghaus E, Smestad C, Mero IL, Aarseth JH, Myhr KM, Celius EG, Lie BA, Karlsen TH, Franke A, Harbo HF.
    J Neuroimmunol; 2010 Sep 14; 226(1-2):194-7. PubMed ID: 20692050
    [Abstract] [Full Text] [Related]

  • 30. Effect of BSN-MST1 locus on inflammatory bowel disease and multiple sclerosis susceptibility.
    Márquez A, Cénit MC, Núñez C, Mendoza JL, Taxonera C, Díaz-Rubio M, Bartolomé M, Arroyo R, Fernández-Arquero M, de la Concha EG, Urcelay E.
    Genes Immun; 2009 Oct 14; 10(7):631-5. PubMed ID: 19657358
    [Abstract] [Full Text] [Related]

  • 31. The tag SNP for HLA-DRB1*1501, rs3135388, is significantly associated with multiple sclerosis susceptibility: cost-effective high-throughput detection by real-time PCR.
    Zivković M, Stanković A, Dincić E, Popović M, Popović S, Raicević R, Alavantić D.
    Clin Chim Acta; 2009 Aug 14; 406(1-2):27-30. PubMed ID: 19433080
    [Abstract] [Full Text] [Related]

  • 32. Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis.
    Cournu-Rebeix I, Génin E, Lesca G, Azoulay-Cayla A, Tubridy N, Noé E, Clanet M, Edan G, Clerget-Darpoux F, Sémana G, Fontaine B.
    Genes Immun; 2003 Oct 14; 4(7):518-23. PubMed ID: 14551606
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34.
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  • 35. Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients.
    Sun J, Lange EM, Isaacs SD, Liu W, Wiley KE, Lange L, Gronberg H, Duggan D, Carpten JD, Walsh PC, Xu J, Chang BL, Isaacs WB, Zheng SL.
    Prostate; 2008 Apr 01; 68(5):489-97. PubMed ID: 18213635
    [Abstract] [Full Text] [Related]

  • 36. Exploration of methods to identify polymorphisms associated with variation in DNA repair capacity phenotypes.
    Jones IM, Thomas CB, Xi T, Mohrenweiser HW, Nelson DO.
    Mutat Res; 2007 Mar 01; 616(1-2):213-20. PubMed ID: 17145065
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  • 37.
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  • 39. Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
    Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J.
    Mol Psychiatry; 2007 Oct 01; 12(10):923-33. PubMed ID: 17579611
    [Abstract] [Full Text] [Related]

  • 40. Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland.
    Pihlaja H, Rantamäki T, Wikström J, Sumelahti ML, Laaksonen M, Ilonen J, Ruutiainen J, Pirttilä T, Elovaara I, Reunanen M, Kuokkanen S, Peltonen L, Koivisto K, Tienari PJ.
    Genes Immun; 2003 Mar 01; 4(2):138-46. PubMed ID: 12618862
    [Abstract] [Full Text] [Related]


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