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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

108 related items for PubMed ID: 17308297

  • 1.
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  • 2. H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.
    van Rheenen W, Diekstra FP, van Doormaal PT, Seelen M, Kenna K, McLaughlin R, Shatunov A, Czell D, van Es MA, van Vught PW, van Damme P, Smith BN, Waibel S, Schelhaas HJ, van der Kooi AJ, de Visser M, Weber M, Robberecht W, Hardiman O, Shaw PJ, Shaw CE, Morrison KE, Al-Chalabi A, Andersen PM, Ludolph AC, Veldink JH, van den Berg LH.
    Neurobiol Aging; 2013 May; 34(5):1517.e5-7. PubMed ID: 23063643
    [Abstract] [Full Text] [Related]

  • 3. H63D HFE polymorphisms are associated with increased disease duration and decreased muscle superoxide dismutase-1 expression in amyotrophic lateral sclerosis patients.
    Su XW, Lee SY, Mitchell RM, Stephens HE, Simmons Z, Connor JR.
    Muscle Nerve; 2013 Aug; 48(2):242-6. PubMed ID: 23813494
    [Abstract] [Full Text] [Related]

  • 4. The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
    Sutedja NA, Sinke RJ, Van Vught PW, Van der Linden MW, Wokke JH, Van Duijn CM, Njajou OT, Van der Schouw YT, Veldink JH, Van den Berg LH.
    Arch Neurol; 2007 Jan; 64(1):63-7. PubMed ID: 17210810
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  • 5. H63D HFE genotype accelerates disease progression in animal models of amyotrophic lateral sclerosis.
    Nandar W, Neely EB, Simmons Z, Connor JR.
    Biochim Biophys Acta; 2014 Dec; 1842(12 Pt A):2413-26. PubMed ID: 25283820
    [Abstract] [Full Text] [Related]

  • 6. HFE p.H63D polymorphism does not influence ALS phenotype and survival.
    Chiò A, Mora G, Sabatelli M, Caponnetto C, Lunetta C, Traynor BJ, Johnson JO, Nalls MA, Calvo A, Moglia C, Borghero G, Monsurrò MR, La Bella V, Volanti P, Simone I, Salvi F, Logullo FO, Nilo R, Giannini F, Mandrioli J, Tanel R, Murru MR, Mandich P, Zollino M, Conforti FL, Penco S, ITALSGEN consortium, SARDINIALS consortium, Brunetti M, Barberis M, Restagno G.
    Neurobiol Aging; 2015 Oct; 36(10):2906.e7-11. PubMed ID: 26174855
    [Abstract] [Full Text] [Related]

  • 7. Mutations in the HFE gene and sporadic amyotrophic lateral sclerosis risk: a meta-analysis of observational studies.
    Li M, Wang L, Wang W, Qi XL, Tang ZY.
    Braz J Med Biol Res; 2014 Feb; 47(3):215-22. PubMed ID: 24604426
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  • 8. H63D polymorphism in the hemochromatosis gene is associated with sporadic amyotrophic lateral sclerosis in China.
    He X, Lu X, Hu J, Xi J, Zhou D, Shang H, Liu L, Zhou H, Yan B, Yu L, Hu F, Liu Z, He L, Yao X, Xu Y.
    Eur J Neurol; 2011 Feb; 18(2):359-361. PubMed ID: 20642794
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  • 9. Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis.
    Praline J, Blasco H, Vourc'h P, Rat V, Gendrot C, Camu W, Andres CR, French ALS Study Group.
    J Neurol Sci; 2012 Jun 15; 317(1-2):58-61. PubMed ID: 22425014
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  • 10. Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences.
    Wang XS, Lee S, Simmons Z, Boyer P, Scott K, Liu W, Connor J.
    J Neurol Sci; 2004 Dec 15; 227(1):27-33. PubMed ID: 15546588
    [Abstract] [Full Text] [Related]

  • 11. Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALS.
    Goodall EF, Greenway MJ, van Marion I, Carroll CB, Hardiman O, Morrison KE.
    Neurology; 2005 Sep 27; 65(6):934-7. PubMed ID: 16186539
    [Abstract] [Full Text] [Related]

  • 12. Mutant HFE H63D protein is associated with prolonged endoplasmic reticulum stress and increased neuronal vulnerability.
    Liu Y, Lee SY, Neely E, Nandar W, Moyo M, Simmons Z, Connor JR.
    J Biol Chem; 2011 Apr 15; 286(15):13161-70. PubMed ID: 21349849
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  • 14. H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population.
    Zhang QQ, Jiang H, Li CY, Liu YL, Tian XY.
    J Integr Neurosci; 2020 Sep 30; 19(3):495-499. PubMed ID: 33070529
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  • 17. Prevalence of HFE (hemochromatosis) gene mutations C282Y and H63D in a Romanian population.
    Voicu PM, Cojocariu C, Petrescu-Danila E, Covic M, Stanciu C, Rusu M.
    Blood Cells Mol Dis; 2009 Sep 30; 42(1):14-5. PubMed ID: 18842428
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  • 20. Haemochromatosis gene (HFE) polymorphisms and migraine: an association study.
    Rainero I, Rubino E, Rivoiro C, Valfrè W, Binello E, Zampella E, De Martino P, Gentile S, Fenoglio P, Savi L, Gallone S, Pinessi L.
    Cephalalgia; 2007 Jan 30; 27(1):9-13. PubMed ID: 17212677
    [Abstract] [Full Text] [Related]

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