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Journal Abstract Search

122 related items for PubMed ID: 11284995

  • 41. A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course.
    Georgoulopoulou E, Gellera C, Bragato C, Sola P, Chiari A, Bernabei C, Mandrioli J.
    Muscle Nerve; 2010 Oct; 42(4):596-7. PubMed ID: 20740631
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  • 42. Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis.
    Bowling AC, Barkowski EE, McKenna-Yasek D, Sapp P, Horvitz HR, Beal MF, Brown RH.
    J Neurochem; 1995 May; 64(5):2366-9. PubMed ID: 7722523
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  • 43. 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; 129 Suppl():90-2. PubMed ID: 7595631
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  • 44. Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation.
    Jonsson PA, Graffmo KS, Andersen PM, Marklund SL, Brännström T.
    Neurobiol Dis; 2009 Dec; 36(3):421-4. PubMed ID: 19703565
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  • 45. [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; 36(3):485-7. PubMed ID: 8741355
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  • 46. 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; 26(2):274-8. PubMed ID: 12210393
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  • 52. An ALS case with a novel D90N-SOD1 heterozygous missense mutation.
    Calvo A, Ilardi A, Moglia C, Canosa A, Carrara G, Valentini C, Ossola I, Brunetti M, Restagno G, Chiò A.
    Amyotroph Lateral Scler; 2012 Jun; 13(4):393-5. PubMed ID: 22632444
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  • 53. Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients.
    Andersen PM, Forsgren L, Binzer M, Nilsson P, Ala-Hurula V, Keränen ML, Bergmark L, Saarinen A, Haltia T, Tarvainen I, Kinnunen E, Udd B, Marklund SL.
    Brain; 1996 Aug; 119 ( Pt 4)():1153-72. PubMed ID: 8813280
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  • 55. 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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  • 56. SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.
    Battistini S, Giannini F, Greco G, Bibbò G, Ferrera L, Marini V, Causarano R, Casula M, Lando G, Patrosso MC, Caponnetto C, Origone P, Marocchi A, Del Corona A, Siciliano G, Carrera P, Mascia V, Giagheddu M, Carcassi C, Orrù S, Garrè C, Penco S.
    J Neurol; 2005 Jul 15; 252(7):782-8. PubMed ID: 15789135
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