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Journal Abstract Search

191 related items for PubMed ID: 21208036

  • 41. Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients.
    Lattante S, Marangi G, Luigetti M, Conte A, Mandrioli J, Del Grande A, Zollino M, Sabatelli M.
    Amyotroph Lateral Scler; 2012 Feb; 13(2):241-2. PubMed ID: 22292847
    [No Abstract] [Full Text] [Related]

  • 42. [Causative genes for familial amyotrophic lateral sclerosis].
    Hadano S.
    Seikagaku; 2002 Jun; 74(6):483-9. PubMed ID: 12138710
    [No Abstract] [Full Text] [Related]

  • 43. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene.
    Tortelli R, Conforti FL, Cortese R, D'Errico E, Distaso E, Mazzei R, Ungaro C, Magariello A, Gambardella A, Logroscino G, Simone IL.
    Neurobiol Aging; 2013 Jun; 34(6):1709.e3-5. PubMed ID: 23182243
    [Abstract] [Full Text] [Related]

  • 44. Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers.
    Freischmidt A, Müller K, Zondler L, Weydt P, Volk AE, Božič AL, Walter M, Bonin M, Mayer B, von Arnim CA, Otto M, Dieterich C, Holzmann K, Andersen PM, Ludolph AC, Danzer KM, Weishaupt JH.
    Brain; 2014 Nov; 137(Pt 11):2938-50. PubMed ID: 25193138
    [Abstract] [Full Text] [Related]

  • 45. [Progress in the field of neurology in the last 100 years: History of research in amyotrophic lateral sclerosis].
    Mannen T.
    Nihon Naika Gakkai Zasshi; 2002 Aug 10; 91(8):2349-53. PubMed ID: 12373847
    [No Abstract] [Full Text] [Related]

  • 46. Disease penetrance in amyotrophic lateral sclerosis associated with mutations in the SOD1 gene.
    Andersen PM, Restagno G, Stewart HG, Chiò A.
    Ann Neurol; 2004 Feb 10; 55(2):298-9; author reply 299. PubMed ID: 14755739
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  • 48. [Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with an H43R mutation in Cu/Zn superoxide dismutase].
    Mochizuki Y, Mizutani T, Nakano R, Fukushima T, Honma T, Nemoto N, Takei K.
    Rinsho Shinkeigaku; 2003 Aug 10; 43(8):491-5. PubMed ID: 14658402
    [Abstract] [Full Text] [Related]

  • 49. [From gene to disease: amyotrophic lateral sclerosis].
    van Vught PW, Veldink JH, Baas F, van Muiswinkel FL, van den Berg LH.
    Ned Tijdschr Geneeskd; 2004 Oct 23; 148(43):2125-7. PubMed ID: 15553356
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  • 53. [Familial amyotrophic lateral sclerosis and a mutation of Cu/Zn superoxide dismutase gene].
    Nakano R, Tsuji S.
    No To Shinkei; 1995 Jun 23; 47(6):529-34. PubMed ID: 7605679
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  • 56. 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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