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Journal Abstract Search

255 related items for PubMed ID: 19411082

  • 1. Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.
    Kamada M, Maruyama H, Tanaka E, Morino H, Wate R, Ito H, Kusaka H, Kawano Y, Miki T, Nodera H, Izumi Y, Kaji R, Kawakami H.
    J Neurol Sci; 2009 Sep 15; 284(1-2):69-71. PubMed ID: 19411082
    [Abstract] [Full Text] [Related]

  • 2. 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 15; 113(5):535-42. PubMed ID: 17333220
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  • 3. TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.
    Maekawa S, Leigh PN, King A, Jones E, Steele JC, Bodi I, Shaw CE, Hortobagyi T, Al-Sarraj S.
    Neuropathology; 2009 Dec 15; 29(6):672-83. PubMed ID: 19496940
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  • 4. 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 15; 61(5):427-34. PubMed ID: 17469116
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 49(4):258-63. PubMed ID: 22499346
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  • 6. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.
    Tsai CP, Soong BW, Lin KP, Tu PH, Lin JL, Lee YC.
    Neurobiol Aging; 2011 Mar 15; 32(3):553.e13-21. PubMed ID: 20472325
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  • 7. Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations.
    Chiò A, Calvo A, Moglia C, Restagno G, Ossola I, Brunetti M, Montuschi A, Cistaro A, Ticca A, Traynor BJ, Schymick JC, Mutani R, Marrosu MG, Murru MR, Borghero G.
    Arch Neurol; 2010 Aug 15; 67(8):1002-9. PubMed ID: 20697052
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  • 13. Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis.
    van Es MA, Dahlberg C, Birve A, Veldink JH, van den Berg LH, Andersen PM.
    J Neurol Neurosurg Psychiatry; 2010 May 15; 81(5):562-6. PubMed ID: 19965850
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  • 14. Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.
    Chen S, Zhou RL, Zhang W, Che CH, Feng SY, Huang HP, Liu CY, Zou ZY.
    Neurobiol Aging; 2021 Nov 15; 107():168-173. PubMed ID: 34175147
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  • 15. Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
    van Blitterswijk M, van Es MA, Hennekam EA, Dooijes D, van Rheenen W, Medic J, Bourque PR, Schelhaas HJ, van der Kooi AJ, de Visser M, de Bakker PI, Veldink JH, van den Berg LH.
    Hum Mol Genet; 2012 Sep 01; 21(17):3776-84. PubMed ID: 22645277
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  • 16. Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease.
    Lattante S, Conte A, Zollino M, Luigetti M, Del Grande A, Marangi G, Romano A, Marcaccio A, Meleo E, Bisogni G, Rossini PM, Sabatelli M.
    Neurology; 2012 Jul 03; 79(1):66-72. PubMed ID: 22722621
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  • 17. Mutational analysis of the Cu/Zn superoxide dismutase gene in a Catalan ALS population: should all sporadic ALS cases also be screened for SOD1?
    Gamez J, Corbera-Bellalta M, Nogales G, Raguer N, García-Arumí E, Badia-Canto M, Lladó-Carbó E, Alvarez-Sabín J.
    J Neurol Sci; 2006 Aug 15; 247(1):21-8. PubMed ID: 16674979
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  • 18. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
    Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noël L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V.
    J Med Genet; 2010 Aug 15; 47(8):554-60. PubMed ID: 20577002
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  • 19. Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.
    Kühnlein P, Sperfeld AD, Vanmassenhove B, Van Deerlin V, Lee VM, Trojanowski JQ, Kretzschmar HA, Ludolph AC, Neumann M.
    Arch Neurol; 2008 Sep 15; 65(9):1185-9. PubMed ID: 18779421
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  • 20. Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
    Rutherford NJ, Zhang YJ, Baker M, Gass JM, Finch NA, Xu YF, Stewart H, Kelley BJ, Kuntz K, Crook RJ, Sreedharan J, Vance C, Sorenson E, Lippa C, Bigio EH, Geschwind DH, Knopman DS, Mitsumoto H, Petersen RC, Cashman NR, Hutton M, Shaw CE, Boylan KB, Boeve B, Graff-Radford NR, Wszolek ZK, Caselli RJ, Dickson DW, Mackenzie IR, Petrucelli L, Rademakers R.
    PLoS Genet; 2008 Sep 19; 4(9):e1000193. PubMed ID: 18802454
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