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Journal Abstract Search

73 related items for PubMed ID: 18042235

  • 1. Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.
    Venturelli E, Villa C, Scarpini E, Fenoglio C, Guidi I, Lovati C, Marcone A, Cortini F, Scalabrini D, Clerici F, Bresolin N, Mariani C, Cappa S, Galimberti D.
    Eur J Neurol; 2008 Jan; 15(1):77-81. PubMed ID: 18042235
    [Abstract] [Full Text] [Related]

  • 2. The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
    Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Ghidoni R, Cortini F, Scalabrini D, Gallone S, Rainero I, Mandelli A, Restelli I, Binetti G, Cappa S, Mariani C, Giordana MT, Bresolin N, Scarpini E, Galimberti D.
    Eur J Neurol; 2009 Jan; 16(1):37-42. PubMed ID: 19087148
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  • 3. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
    Ingelsson M, Ramasamy K, Russ C, Freeman SH, Orne J, Raju S, Matsui T, Growdon JH, Frosch MP, Ghetti B, Brown RH, Irizarry MC, Hyman BT.
    Acta Neuropathol; 2007 Nov; 114(5):471-9. PubMed ID: 17721707
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  • 4. MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels.
    Galimberti D, Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Cortini F, Scalabrini D, Perini L, Restelli I, Binetti G, Cappa S, Mariani C, Bresolin N, Scarpini E.
    J Alzheimers Dis; 2009 Nov; 17(1):125-33. PubMed ID: 19494437
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  • 5. Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.
    Josephs KA, Petersen RC, Knopman DS, Boeve BF, Whitwell JL, Duffy JR, Parisi JE, Dickson DW.
    Neurology; 2006 Jan 10; 66(1):41-8. PubMed ID: 16401843
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  • 6. Lack of association between the C276T polymorphism of the neuronal nitric oxide synthase gene and migraine.
    Alaşehirli B, Akçalı A, Demiryürek AT, Özel A, Erdal ME, Neyal M.
    Int J Neurosci; 2013 Jan 10; 123(1):50-4. PubMed ID: 22937753
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  • 7. TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease.
    Johansson A, Zetterberg H, Håkansson A, Nissbrandt H, Blennow K.
    Neurodegener Dis; 2005 Jan 10; 2(1):28-35. PubMed ID: 16909000
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  • 9. Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degeneration.
    Borroni B, Ghezzi S, Agosti C, Archetti S, Fenoglio C, Galimberti D, Scarpini E, Di Luca M, Bresolin N, Comi GP, Padovani A, Del Bo R.
    Rejuvenation Res; 2008 Aug 10; 11(4):773-80. PubMed ID: 18729809
    [Abstract] [Full Text] [Related]

  • 10. Alcohol dehydrogenase 2 genotype and risk for migraine.
    García-Martín E, Martínez C, Serrador M, Alonso-Navarro H, Navacerrada F, Agúndez JA, Jiménez-Jiménez FJ.
    Headache; 2010 Jan 10; 50(1):85-91. PubMed ID: 19486361
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  • 11. Association between achalasia and nitric oxide synthase gene polymorphisms.
    Mearin F, García-González MA, Strunk M, Zárate N, Malagelada JR, Lanas A.
    Am J Gastroenterol; 2006 Sep 10; 101(9):1979-84. PubMed ID: 16848803
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  • 12. BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease.
    Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Cortini F, Serpente M, Cantoni C, Fumagalli G, Ridolfi E, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D.
    J Alzheimers Dis; 2011 Sep 10; 23(4):701-7. PubMed ID: 21157029
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  • 13. Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.
    Villa C, Fenoglio C, De Riz M, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Cortini F, Serpente M, Cantoni C, Fumagalli G, Martinelli Boneschi F, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D.
    Rejuvenation Res; 2011 Jun 10; 14(3):275-81. PubMed ID: 21548758
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  • 19. Increased frequency of positive family history of dementia in sporadic CJD.
    Krasnianski A, von Ahsen N, Heinemann U, Meissner B, Schulz-Schaeffer WJ, Kretzschmar HA, Armstrong VW, Zerr I.
    Neurobiol Aging; 2009 Apr 10; 30(4):615-21. PubMed ID: 17822808
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