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Volumn 51, Issue 3, 1998, Pages 871-873

Familial amyotrophic lateral sclerosis with widespread vacuolation and hyaline inclusions

Author keywords

[No Author keywords available]

Indexed keywords

SUPEROXIDE DISMUTASE;

EID: 0031751093     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.3.871     Document Type: Article
Times cited : (17)

References (10)
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    • Gurney, M.E.1    Pu, H.2    Chiu, A.Y.3
  • 2
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    • Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis
    • Dal Canto MC, Gurney ME. Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis. Am J Pathol 1994;145:1271-1280.
    • (1994) Am J Pathol , vol.145 , pp. 1271-1280
    • Dal Canto, M.C.1    Gurney, M.E.2
  • 3
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    • An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
    • Wong PC, Pardo CA, Borchelt DR, et al. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 1995;14:1105-1116.
    • (1995) Neuron , vol.14 , pp. 1105-1116
    • Wong, P.C.1    Pardo, C.A.2    Borchelt, D.R.3
  • 4
    • 0029966363 scopus 로고    scopus 로고
    • Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions
    • Tu PH, Raju P, Robinson KA, Gurney ME, Trojanowski JQ, Lee VM-Y. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proc Natl Acad Sci USA 1996;93:3155-3160.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 3155-3160
    • Tu, P.H.1    Raju, P.2    Robinson, K.A.3    Gurney, M.E.4    Trojanowski, J.Q.5    Lee, V.M.-Y.6
  • 5
    • 0031051485 scopus 로고    scopus 로고
    • ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions
    • Bruijn LI, Becher MW, Lee MK, et al. ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions. Neuron 1997;18:327-338.
    • (1997) Neuron , vol.18 , pp. 327-338
    • Bruijn, L.I.1    Becher, M.W.2    Lee, M.K.3
  • 6
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    • Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene
    • Takahashi H, Makifuchi T, Nakano R, et al. Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene. Acta Neuropathol 1994;88:185-188.
    • (1994) Acta Neuropathol , vol.88 , pp. 185-188
    • Takahashi, H.1    Makifuchi, T.2    Nakano, R.3
  • 7
    • 0029840428 scopus 로고    scopus 로고
    • Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1 gene: Multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes
    • Kato S, Shimoda M, Watanabe Y, Nakashima K, Takahashi K, Ohama E. Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1 gene: multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes. J Neuropathol Exp Neurol 1996;55:1089-1101.
    • (1996) J Neuropathol Exp Neurol , vol.55 , pp. 1089-1101
    • Kato, S.1    Shimoda, M.2    Watanabe, Y.3    Nakashima, K.4    Takahashi, K.5    Ohama, E.6
  • 8
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    • Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: Pathological and immunocytochemical changes
    • Ince PG, Shaw PJ, Slade JY, Jones C, Hudgson P. Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changes. Acta Neuropathol 1996;92:395-403.
    • (1996) Acta Neuropathol , vol.92 , pp. 395-403
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  • 10
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    • Presence of Cu/Zn superoxide dismutase (SOD) immunoreactivity in neuronal hyaline inclusions in spinal cords from mice carrying a transgene for Gly 93 Ala mutant human Cu/Zn SOD
    • Shibata N, Hirano A, Kobayashi M, et al. Presence of Cu/Zn superoxide dismutase (SOD) immunoreactivity in neuronal hyaline inclusions in spinal cords from mice carrying a transgene for Gly 93 Ala mutant human Cu/Zn SOD. Acta Neuropathol 1998;95:136-142.
    • (1998) Acta Neuropathol , vol.95 , pp. 136-142
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.