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Journal Abstract Search

205 related items for PubMed ID: 14517684

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  • 3. Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions.
    Ohi T, Nabeshima K, Kato S, Yazawa S, Takechi S.
    J Neurol Sci; 2004 Oct 15; 225(1-2):19-25. PubMed ID: 15465081
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  • 4. 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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  • 5. Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
    Kato S, Sumi-Akamaru H, Fujimura H, Sakoda S, Kato M, Hirano A, Takikawa M, Ohama E.
    Acta Neuropathol; 2001 Sep 15; 102(3):233-8. PubMed ID: 11585247
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  • 8. 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
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  • 9. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
    Kato S, Funakoshi H, Nakamura T, Kato M, Nakano I, Hirano A, Ohama E.
    Acta Neuropathol; 2003 Aug 15; 106(2):112-20. PubMed ID: 12707786
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  • 10. [Different clinical phenotypes of siblings with familial amyotrophic lateral sclerosis showing Cys146Arg point mutation of superoxide dismutase 1 gene].
    Ito K, Uchiyama T, Fukutake T, Arai K, Kanesaka T, Hattori T.
    Rinsho Shinkeigaku; 2002 Feb 15; 42(2):175-7. PubMed ID: 12424972
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  • 11. 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 15; 136(1-2):108-16. PubMed ID: 8815157
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  • 12. 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 15; 18(6):639-47. PubMed ID: 9876871
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  • 15. [Familial amyotrophic lateral sclerosis (FALS) with a novel SOD1 gene mutation: a clinicopathological study].
    Kawamata C, Morita M, Shibata N, Nakano I.
    Rinsho Shinkeigaku; 2007 May 15; 47(5):211-6. PubMed ID: 17585602
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  • 17. 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 15; 100(6):603-7. PubMed ID: 11078211
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  • 19. Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.
    Kato S, Saito M, Hirano A, Ohama E.
    Histol Histopathol; 1999 Jul 15; 14(3):973-89. PubMed ID: 10425565
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  • 20. Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase.
    Ohi T, Saita K, Takechi S, Nabesima K, Tashiro H, Shiomi K, Sugimoto S, Akematsu T, Nakayama T, Iwaki T, Matsukura S.
    J Neurol Sci; 2002 May 15; 197(1-2):73-8. PubMed ID: 11997070
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