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PUBMED FOR HANDHELDS

Journal Abstract Search


132 related items for PubMed ID: 16764352

  • 1. No association of CCR5delta32 gene mutation with multiple sclerosis in Croatian and Slovenian patients.
    Ristić S, Lovrecić L, Starcević-Cizmarević N, Brajenović-Milić B, Jazbec SS, Barac-Latas V, Vejnović D, Sepcić J, Kapović M, Peterlin B.
    Mult Scler; 2006 Jun; 12(3):360-2. PubMed ID: 16764352
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  • 3. Increase in CCR5 Delta32/Delta32 genotype in multiple sclerosis.
    Pulkkinen K, Luomala M, Kuusisto H, Lehtimäki T, Saarela M, Jalonen TO, Elovaara I.
    Acta Neurol Scand; 2004 May; 109(5):342-7. PubMed ID: 15080861
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  • 4. Tumor necrosis factor-alpha-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients.
    Ristić S, Lovrecić L, Starcević-Cizmarević N, Brajenović-Milić B, Sega Jazbec S, Sepcić J, Kapović M, Peterlin B.
    Eur Neurol; 2007 May; 57(4):203-7. PubMed ID: 17268200
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  • 5. CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients.
    Cizmarević NS, Gašparović I, Peterlin B, Sepčić J, Rudolf G, Kapović M, Lavtar P, Ristić S.
    Int J Immunogenet; 2011 Oct; 38(5):419-26. PubMed ID: 21797987
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  • 7. Genetic analysis of SLC11A1 polymorphisms in multiple sclerosis patients.
    Comabella M, Altet L, Peris F, Villoslada P, Sánchez A, Montalban X.
    Mult Scler; 2004 Dec; 10(6):618-20. PubMed ID: 15584484
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  • 8. CCR5Δ32 - A piece of protection in the inflammatory puzzle of multiple sclerosis susceptibility.
    Troncoso LL, Pontillo A, Oliveira EML, Finkelszteijn A, Schneider S, Chies JAB.
    Hum Immunol; 2018 Aug; 79(8):621-626. PubMed ID: 29729320
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  • 13. 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; 17(5):740-5. PubMed ID: 20067515
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  • 15. 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
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  • 17. The p150 subunit of dynactin (DCTN1) gene in multiple sclerosis.
    Münch C, Meyer R, Linke P, Meyer T, Ludolph AC, Haas J, Hemmer B.
    Acta Neurol Scand; 2007 Oct; 116(4):231-4. PubMed ID: 17824900
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  • 19. Multiple sclerosis risk: interaction between human leukocyte antigen and the environment in Sardinian population.
    Cocco E, Sardu C, Murru R, Frau J, Lorefice L, Mamusa E, Contu P, Marrosu MG.
    Mult Scler; 2009 Sep; 15(9):1030-6. PubMed ID: 19625333
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