These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 18397664)

  • 1. [Multiple sclerosis--the significance of genes. The Danish Society of Neurology].
    Sellebjerg F; Oturai A; Sørensen PS;
    Ugeskr Laeger; 2008 Mar; 170(12):1046. PubMed ID: 18397664
    [No Abstract]   [Full Text] [Related]  

  • 2. [Towards the discovery of genes predisposing to multiple sclerosis].
    Seboun E
    Pathol Biol (Paris); 1994 Nov; 42(9):821-5. PubMed ID: 7753589
    [No Abstract]   [Full Text] [Related]  

  • 3. Genomewide study of multiple sclerosis.
    Chaudhuri A; Behan PO
    N Engl J Med; 2007 Nov; 357(21):2200; author reply 2200-1. PubMed ID: 18038461
    [No Abstract]   [Full Text] [Related]  

  • 4. Genetics of multiple sclerosis.
    Oksenberg JR; Hauser SL
    Neurol Clin; 2005 Feb; 23(1):61-75, vi. PubMed ID: 15661088
    [No Abstract]   [Full Text] [Related]  

  • 5. Chromosome 7q21-22 and multiple sclerosis.
    Villoslada P; Barcellos LF; Oksenberg JR
    J Neuroimmunol; 2004 May; 150(1-2):1-2. PubMed ID: 15081242
    [No Abstract]   [Full Text] [Related]  

  • 6. An overview of gene-epigenetic-environmental contributions to MS causation.
    Lincoln JA; Cook SD
    J Neurol Sci; 2009 Nov; 286(1-2):54-7. PubMed ID: 19616791
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The genetics of multiple sclerosis: SNPs to pathways to pathogenesis.
    Oksenberg JR; Baranzini SE; Sawcer S; Hauser SL
    Nat Rev Genet; 2008 Jul; 9(7):516-26. PubMed ID: 18542080
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The genetics of clinical outcome in multiple sclerosis.
    Ramagopalan SV; Deluca GC; Degenhardt A; Ebers GC
    J Neuroimmunol; 2008 Sep; 201-202():183-99. PubMed ID: 18632165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No evidence for association between the EIF2B5 gene and multiple sclerosis in French families.
    Fogli A; Barbier C; Cournu-Rebeix I; Babron MC; Clerget-Darpoux F; Fontaine B; Boespflug-Tanguy O
    Mult Scler; 2008 May; 14(4):573. PubMed ID: 18562513
    [No Abstract]   [Full Text] [Related]  

  • 10. The SH2D2A gene and susceptibility to multiple sclerosis.
    Lorentzen AR; Smestad C; Lie BA; Oturai AB; Akesson E; Saarela J; Myhr KM; Vartdal F; Celius EG; Sørensen PS; Hillert J; Spurkland A; Harbo HF
    J Neuroimmunol; 2008 Jul; 197(2):152-8. PubMed ID: 18554728
    [TBL] [Abstract][Full Text] [Related]  

  • 11. APOE epsilon4 allele is associated with cognitive impairment in patients with multiple sclerosis.
    Mazurek AA; Shi J
    Neurology; 2008 Oct; 71(15):1203; author reply 1203. PubMed ID: 18838671
    [No Abstract]   [Full Text] [Related]  

  • 12. Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.
    Perera D; Stankovich J; Butzkueven H; Taylor BV; Foote SJ; Kilpatrick TJ; Rubio JP
    J Neuroimmunol; 2009 Jun; 211(1-2):105-9. PubMed ID: 19375175
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 213(1-2):142-7. PubMed ID: 19515430
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Re: GAMES issue.
    Ebers GC; Sadovnik AD
    J Neuroimmunol; 2004 Aug; 153(1-2):4-5. PubMed ID: 15334747
    [No Abstract]   [Full Text] [Related]  

  • 15. Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families.
    Ramagopalan SV; Morrison KM; Para A; Handel A; Disanto G; Handunnetthi L; Orton SM; Sadovnick AD; Ebers GC
    J Neuroimmunol; 2009 Jul; 212(1-2):142-4. PubMed ID: 19428123
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Re: GAMES issue study: Are international genetic consortia functional?
    De Jager PL; Walsh EC; Rioux JD; Hafler DA
    J Neuroimmunol; 2004 Aug; 153(1-2):5-6. PubMed ID: 15334748
    [No Abstract]   [Full Text] [Related]  

  • 17. Reproductive issues in persons with multiple sclerosis.
    Giesser B
    Del Med J; 2004 Mar; 76(3):125-8. PubMed ID: 15061459
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetic polymorphism at codon 129 of the prion protein gene is not associated with multiple sclerosis.
    Stüve O; Korth C; Gabatto P; Cameron EM; Hu W; Eagar TN; Monson NL; Frohman EM; Racke MK; Zabetian CP; Oksenberg JR
    Arch Neurol; 2009 Feb; 66(2):280-1. PubMed ID: 19204171
    [No Abstract]   [Full Text] [Related]  

  • 19. EVI5 is a risk gene for multiple sclerosis.
    Hoppenbrouwers IA; Aulchenko YS; Ebers GC; Ramagopalan SV; Oostra BA; van Duijn CM; Hintzen RQ
    Genes Immun; 2008 Jun; 9(4):334-7. PubMed ID: 18401352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. KIR2DL4 (CD158d) polymorphisms and susceptibility to multiple sclerosis.
    Goris A; Dobosi R; Boonen S; Nagels G; Dubois B
    J Neuroimmunol; 2009 May; 210(1-2):113-5. PubMed ID: 19304328
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.