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Journal Abstract Search

183 related items for PubMed ID: 9876871

  • 1. Molecular analyses of the Cu/Zn superoxide dismutase gene in patients with familial amyotrophic lateral sclerosis (ALS) in Japan.
    Aoki M, Abe K, Itoyama Y.
    Cell Mol Neurobiol; 1998 Dec; 18(6):639-47. PubMed ID: 9876871
    [Abstract] [Full Text] [Related]

  • 2. Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations.
    Abe K, Aoki M, Ikeda M, Watanabe M, Hirai S, Itoyama Y.
    J Neurol Sci; 1996 Mar; 136(1-2):108-16. PubMed ID: 8815157
    [Abstract] [Full Text] [Related]

  • 3. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS.
    Aoki M, Ogasawara M, Matsubara Y, Narisawa K, Nakamura S, Itoyama Y, Abe K.
    J Neurol Sci; 1994 Oct; 126(1):77-83. PubMed ID: 7836951
    [Abstract] [Full Text] [Related]

  • 4. A clinical variance in familial amyotrophic lateral sclerosis with a point mutation in Cu/Zn superoxide dismutase gene.
    Sakuma R, Abe K, Aoki M, Ikeda M, Okita N, Hiwatari M, Sakurai M, Itoyama Y.
    Eur J Neurol; 1995 Sep; 2(4):369-74. PubMed ID: 24283690
    [Abstract] [Full Text] [Related]

  • 5. Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn superoxide dismutase mutation.
    Aoki M, Abe K, Houi K, Ogasawara M, Matsubara Y, Kobayashi T, Mochio S, Narisawa K, Itoyama Y.
    Ann Neurol; 1995 May; 37(5):676-9. PubMed ID: 7755363
    [Abstract] [Full Text] [Related]

  • 6. A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.
    Zhang H, Zhao H, Lu M, Zhang Y, Wang L, Zhang J, Ma D, Fan D.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Dec; 6(4):234-8. PubMed ID: 16319027
    [Abstract] [Full Text] [Related]

  • 7. [Molecular mechanism of ALS and a possible gene therapy].
    Abe K, Warita H.
    Rinsho Shinkeigaku; 1999 Jan; 39(1):68-9. PubMed ID: 10377808
    [Abstract] [Full Text] [Related]

  • 8. A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis.
    Nakano R, Sato S, Inuzuka T, Sakimura K, Mishina M, Takahashi H, Ikuta F, Honma Y, Fujii J, Taniguchi N.
    Biochem Biophys Res Commun; 1994 Apr 29; 200(2):695-703. PubMed ID: 8179602
    [Abstract] [Full Text] [Related]

  • 9. Variable clinical symptoms in familial amyotrophic lateral sclerosis with a novel point mutation in the Cu/Zn superoxide dismutase gene.
    Ikeda M, Abe K, Aoki M, Sahara M, Watanabe M, Shoji M, St George-Hyslop PH, Hirai S, Itoyama Y.
    Neurology; 1995 Nov 29; 45(11):2038-42. PubMed ID: 7501156
    [Abstract] [Full Text] [Related]

  • 10. [On intra-familial clinical diversities of a familial amyotrophic lateral sclerosis with a point mutation of Cu/Zn superoxide dismutase (Asn 86-Ser].
    Maeda T, Kurahashi K, Matsunaga M, Inoue K, Inoue M.
    No To Shinkei; 1997 Sep 29; 49(9):847-51. PubMed ID: 9311004
    [Abstract] [Full Text] [Related]

  • 11. Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.
    Takazawa T, Ikeda K, Hirayama T, Kawabe K, Nakamura Y, Ito H, Kano O, Yoshii Y, Tanaka F, Sobue G, Iwasaki Y.
    Intern Med; 2010 Sep 29; 49(2):183-6. PubMed ID: 20075587
    [Abstract] [Full Text] [Related]

  • 12. A novel mutation (Cys6Gly) in the Cu/Zn superoxide dismutase gene associated with rapidly progressive familial amyotrophic lateral sclerosis.
    Kohno S, Takahashi Y, Miyajima H, Serizawa M, Mizoguchi K.
    Neurosci Lett; 1999 Dec 03; 276(2):135-7. PubMed ID: 10624810
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  • 17. Superoxide dismutase activity in lymphoblastoid cells from motor neurone disease/amyotrophic lateral sclerosis (MND/ALS) patients.
    Garofalo O, Figlewicz DA, Thomas SM, Butler R, Lebuis L, Rouleau G, Meininger V, Leigh PN.
    J Neurol Sci; 1995 May 03; 129 Suppl():90-2. PubMed ID: 7595631
    [Abstract] [Full Text] [Related]

  • 18. Familial amyotrophic lateral sclerosis with onset in bulbar sign, benign clinical course, and Bunina bodies: a clinical, genetic, and pathological study of a Japanese family.
    Tsuchiya K, Shintani S, Nakabayashi H, Kikugawa K, Nakano R, Haga C, Nakano I, Ikeda K, Tsuji S.
    Acta Neuropathol; 2000 Dec 03; 100(6):603-7. PubMed ID: 11078211
    [Abstract] [Full Text] [Related]

  • 19. Genetics of ALS in Italian families.
    Gellera C.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Mar 03; 2 Suppl 1():S43-6. PubMed ID: 11465924
    [Abstract] [Full Text] [Related]

  • 20. [Familial amyotrophic lateral sclerosis showing variable clinical courses with (Leu84-->Val) mutation of Cu/Zn superoxide dismutase].
    Ohnishi A, Miyazaki S, Murai Y, Ueno S, Sakai H.
    Rinsho Shinkeigaku; 1996 Mar 03; 36(3):485-7. PubMed ID: 8741355
    [Abstract] [Full Text] [Related]

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