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Journal Abstract Search

113 related items for PubMed ID: 7608718

  • 1. Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease.
    Bandmann O, Davis MB, Marsden CD, Harding AE.
    J Neurol Neurosurg Psychiatry; 1995 Jul; 59(1):90-1. PubMed ID: 7608718
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  • 2. Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.
    Orrell RW, Habgood J, Rudge P, Lane RJ, de Belleroche JS.
    Ann Neurol; 1996 Jun; 39(6):810-2. PubMed ID: 8651656
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  • 3. [Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis].
    Shi SG, Li LS, Chen KN, Liu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):149-52. PubMed ID: 15079798
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  • 4. Identification of three mutations in the Cu,Zn-superoxide dismutase (Cu,Zn-SOD) gene with familial amyotrophic lateral sclerosis: transduction of human Cu,Zn-SOD into PC12 cells by HIV-1 TAT protein basic domain.
    Chou CM, Huang CJ, Shih CM, Chen YP, Liu TP, Chen CT.
    Ann N Y Acad Sci; 2005 May; 1042():303-13. PubMed ID: 15965076
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  • 5. The Cu/Zn superoxide dismutase gene in ALS and parkinsonism-dementia of Guam.
    Figlewicz DA, Garruto RM, Krizus A, Yanagihara R, Rouleau GA.
    Neuroreport; 1994 Jan 31; 5(5):557-60. PubMed ID: 8025243
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  • 6. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
    García-Redondo A, Bustos F, Juan Y Seva B, Del Hoyo P, Jiménez S, Campos Y, Martín MA, Rubio JC, Cañadillas F, Arenas J, Esteban J.
    Muscle Nerve; 2002 Aug 31; 26(2):274-8. PubMed ID: 12210393
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  • 7. Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis.
    Deng HX, Tainer JA, Mitsumoto H, Ohnishi A, He X, Hung WY, Zhao Y, Juneja T, Hentati A, Siddique T.
    Hum Mol Genet; 1995 Jun 31; 4(6):1113-6. PubMed ID: 7655471
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  • 9. A novel T137A SOD1 mutation in an Italian family with two subjects affected by amyotrophic lateral sclerosis.
    Visani M, de Biase D, Bartolomei I, Plasmati R, Morandi L, Cenacchi G, Salvi F, Pession A.
    Amyotroph Lateral Scler; 2011 Sep 31; 12(5):385-8. PubMed ID: 21574856
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  • 10. Mutant SOD1 mediated pathogenesis of Amyotrophic Lateral Sclerosis.
    Kaur SJ, McKeown SR, Rashid S.
    Gene; 2016 Feb 15; 577(2):109-18. PubMed ID: 26657039
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  • 14. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
    Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX.
    Nature; 1993 Mar 04; 362(6415):59-62. PubMed ID: 8446170
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  • 15. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase.
    Andersen PM, Nilsson P, Ala-Hurula V, Keränen ML, Tarvainen I, Haltia T, Nilsson L, Binzer M, Forsgren L, Marklund SL.
    Nat Genet; 1995 May 04; 10(1):61-6. PubMed ID: 7647793
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  • 16. [Parkinson disease and amyotrophic lateral sclerosis. Tauopathies, TDP-43 and SOD mutations].
    Le Forestier N, Lacomblez L, Meininger V.
    Rev Neurol (Paris); 2009 Jan 04; 165(1):15-30. PubMed ID: 18808763
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  • 18. A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis.
    Baek W, Koh SH, Park JS, Kim YS, Kim HY, Kwon MJ, Ki CS, Kim SH.
    J Neurol Sci; 2011 Jul 15; 306(1-2):157-9. PubMed ID: 21496827
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  • 19. The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.
    Syriani E, Morales M, Gamez J.
    J Neurol Sci; 2009 Oct 15; 285(1-2):46-53. PubMed ID: 19524271
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