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Journal Abstract Search

198 related items for PubMed ID: 20363033

  • 1. Genetic association of CASP8 polymorphisms with primary progressive multiple sclerosis.
    Camiña-Tato M, Fernández M, Morcillo-Suárez C, Navarro A, Julià E, Edo MC, Montalban X, Comabella M.
    J Neuroimmunol; 2010 May; 222(1-2):70-5. PubMed ID: 20363033
    [Abstract] [Full Text] [Related]

  • 2. Genetic association between polymorphisms in the BTG1 gene and multiple sclerosis.
    Camiña-Tato M, Morcillo-Suárez C, Navarro A, Fernández M, Horga A, Montalban X, Comabella M.
    J Neuroimmunol; 2009 Aug 18; 213(1-2):142-7. PubMed ID: 19515430
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  • 3. Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis.
    Scalabrini D, Fenoglio C, Scarpini E, De Riz M, Comi C, Venturelli E, Cortini F, Piola M, Villa C, Naldi P, Monaco F, Bresolin N, Galimberti D.
    Neurosci Lett; 2007 Oct 02; 425(3):173-6. PubMed ID: 17825989
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  • 6. 3'UTR C2370A allele of the IL-23 receptor gene is associated with relapsing-remitting multiple sclerosis.
    Illes Z, Safrany E, Peterfalvi A, Magyari L, Farago B, Pozsonyi E, Rozsa C, Komoly S, Melegh B.
    Neurosci Lett; 2008 Jan 24; 431(1):36-8. PubMed ID: 18180107
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  • 7. Tumour necrosis factor alpha gene (TNF-alpha) -376 polymorphism in Hungarian patients with primary progressive multiple sclerosis.
    Losonczi E, Bencsik K, Nagy ZF, Honti V, Szalczer E, Rajda C, Illés Z, Mátyás K, Rózsa C, Csépány T, Füvesi J, Vécsei L.
    J Neuroimmunol; 2009 Mar 31; 208(1-2):115-8. PubMed ID: 19201038
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  • 8. 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
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  • 9. Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort.
    Martinelli-Boneschi F, Esposito F, Scalabrini D, Fenoglio C, Rodegher ME, Brambilla P, Colombo B, Ghezzi A, Capra R, Collimedaglia L, Coniglio G, De Riz M, Serpente M, Cantoni C, Scarpini E, Martinelli V, Galimberti D, Comi G.
    Eur J Neurol; 2010 May 15; 17(5):740-5. PubMed ID: 20067515
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  • 10. CASP-9: A susceptibility locus for multiple sclerosis in Italy.
    Andreoli V, Trecroci F, La Russa A, Valentino P, Condino F, Latorre V, Nisticò R, Pirritano D, Del Giudice F, Canino M, Cittadella R, Quattrone A.
    J Neuroimmunol; 2009 May 29; 210(1-2):100-3. PubMed ID: 19359048
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  • 11. An investigation of susceptibility loci in benign, aggressive and primary progressive multiple sclerosis in Northern Irish population.
    Gray OM, Abdeen H, McDonnell GV, Patterson CC, Graham CA, Hawkins SA.
    Mult Scler; 2009 Mar 29; 15(3):299-303. PubMed ID: 19244395
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  • 12. Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosis.
    Camiña-Tato M, Morcillo-Suárez C, Bustamante MF, Ortega I, Navarro A, Muntasell A, López-Botet M, Sánchez A, Carmona P, Julià E, Tortola MT, Audí L, Oksenberg JR, Martin R, Montalban X, Comabella M.
    J Immunol; 2010 Nov 01; 185(9):5392-404. PubMed ID: 20921521
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  • 14. Apolipoprotein E genotype does not associate with disease severity measured by Multiple Sclerosis Severity Score.
    Guerrero AL, Laherrán E, Gutiérrez F, Martín-Polo J, Iglesias F, Alcázar C, Peralta J, Rostami P.
    Acta Neurol Scand; 2008 Jan 01; 117(1):21-5. PubMed ID: 17883422
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  • 15. Interleukin (IL)-1 gene polymorphisms: relevance of disease severity associated alleles with IL-1beta and IL-1ra production in multiple sclerosis.
    Schrijver HM, van As J, Crusius JB, Dijkstra CD, Uitdehaag BM.
    Mediators Inflamm; 2003 Apr 01; 12(2):89-94. PubMed ID: 12775358
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  • 16. Interleukin 18 receptor 1 expression distinguishes patients with multiple sclerosis.
    Gillett A, Thessen Hedreul M, Khademi M, Espinosa A, Beyeen AD, Jagodic M, Kockum I, Harris RA, Olsson T.
    Mult Scler; 2010 Sep 01; 16(9):1056-65. PubMed ID: 20354066
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  • 17. Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients.
    Otaegui D, Zuriarrain O, Castillo-Triviño T, Aransay A, Ruíz-Martinez J, Olaskoaga J, Marti-Masso J, Lopez de Munain A.
    Mult Scler; 2009 Jan 01; 15(1):124-8. PubMed ID: 18755822
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  • 18. Progression of multiple sclerosis is associated with exon 1 CTLA-4 gene polymorphism.
    Bilińska M, Frydecka I, Noga L, Dobosz T, Zołedziewska M, Suwalska K, Tutak A, Pokryszko-Dragan A.
    Acta Neurol Scand; 2004 Jul 01; 110(1):67-71. PubMed ID: 15180809
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  • 19. Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population.
    Myhre R, Toft M, Kachergus J, Hulihan MM, Aasly JO, Klungland H, Farrer MJ.
    Acta Neurol Scand; 2008 Nov 01; 118(5):320-7. PubMed ID: 18485051
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