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Journal Abstract Search

210 related items for PubMed ID: 16107368

  • 21.
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  • 22. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
    Millecamps S, Boillée S, Le Ber I, Seilhean D, Teyssou E, Giraudeau M, Moigneu C, Vandenberghe N, Danel-Brunaud V, Corcia P, Pradat PF, Le Forestier N, Lacomblez L, Bruneteau G, Camu W, Brice A, Cazeneuve C, Leguern E, Meininger V, Salachas F.
    J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
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  • 23. Flumazenil does not affect intracortical motor excitability in humans: a transcranial magnetic stimulation study.
    Jung HY, Sohn YH, Mason A, Considine E, Hallett M.
    Clin Neurophysiol; 2004 Feb; 115(2):325-9. PubMed ID: 14744573
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  • 24. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
    Tan CF, Eguchi H, Tagawa A, Onodera O, Iwasaki T, Tsujino A, Nishizawa M, Kakita A, Takahashi H.
    Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220
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  • 30. [11C]-WAY100635 PET demonstrates marked 5-HT1A receptor changes in sporadic ALS.
    Turner MR, Rabiner EA, Hammers A, Al-Chalabi A, Grasby PM, Shaw CE, Brooks DJ, Leigh PN.
    Brain; 2005 Apr; 128(Pt 4):896-905. PubMed ID: 15689356
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  • 33. Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
    Felbecker A, Camu W, Valdmanis PN, Sperfeld AD, Waibel S, Steinbach P, Rouleau GA, Ludolph AC, Andersen PM.
    J Neurol Neurosurg Psychiatry; 2010 May; 81(5):572-7. PubMed ID: 20460594
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  • 34. DNA sequence analysis of the conserved region around the SOD1 gene locus in recessively inherited ALS.
    Broom WJ, Johnson DV, Garber M, Andersen PM, Lennon N, Landers J, Nusbaum C, Russ C, Brown RH.
    Neurosci Lett; 2009 Sep 29; 463(1):64-9. PubMed ID: 19596401
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  • 35. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
    Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, Cairns NJ, Kwong LK, Forman MS, Ravits J, Stewart H, Eisen A, McClusky L, Kretzschmar HA, Monoranu CM, Highley JR, Kirby J, Siddique T, Shaw PJ, Lee VM, Trojanowski JQ.
    Ann Neurol; 2007 May 29; 61(5):427-34. PubMed ID: 17469116
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  • 37. Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes.
    Broom WJ, Russ C, Sapp PC, McKenna-Yasek D, Hosler BA, Andersen PM, Brown RH.
    Neurosci Lett; 2006 Jan 09; 392(1-2):52-7. PubMed ID: 16174551
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  • 40. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.
    Cudkowicz ME, McKenna-Yasek D, Chen C, Hedley-Whyte ET, Brown RH.
    Ann Neurol; 1998 Jun 09; 43(6):703-10. PubMed ID: 9629839
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