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Journal Abstract Search

210 related items for PubMed ID: 9365366

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  • 3. 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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  • 4. 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; 10(1):61-6. PubMed ID: 7647793
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  • 5. Motor system abnormalities in heterozygous relatives of a D90A homozygous CuZn-SOD ALS patient of finnish extraction.
    Mezei M, Andersen PM, Stewart H, Weber M, Eisen A.
    J Neurol Sci; 1999 Oct 31; 169(1-2):49-55. PubMed ID: 10540007
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  • 9. CuZn-superoxide dismutase, extracellular superoxide dismutase, and glutathione peroxidase in blood from individuals homozygous for Asp90Ala CuZu-superoxide dismutase mutation.
    Andersen PM, Nilsson P, Forsgren L, Marklund SL.
    J Neurochem; 1998 Feb 31; 70(2):715-20. PubMed ID: 9453566
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  • 12. Recessively inherited amyotrophic lateral sclerosis: a Germany family with the D90A CuZn-SOD mutation.
    Winter SM, Claus A, Oberwittler C, Völkel H, Wenzler S, Ludolph AC.
    J Neurol; 2000 Oct 31; 247(10):783-6. PubMed ID: 11127534
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  • 17. Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.
    Skvortsova VI, Limborska SA, Slominsky PA, Levitskaya NI, Levitsky GN, Shadrina MI, Kondratyeva EA.
    Eur J Neurol; 2001 Mar 31; 8(2):167-72. PubMed ID: 11284995
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  • 18. D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis.
    Robberecht W, Aguirre T, Van den Bosch L, Tilkin P, Cassiman JJ, Matthijs G.
    Neurology; 1996 Nov 31; 47(5):1336-9. PubMed ID: 8909456
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  • 19. Sporadic motor neuron disease in a familial novel SOD1 mutation: incomplete penetrance or chance association?
    Conforti FL, Barone R, Fermo SL, Giliberto C, Patti F, Gambardella A, Quattrone A, Zappia M.
    Amyotroph Lateral Scler; 2011 May 31; 12(3):220-2. PubMed ID: 21545237
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  • 20. Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene.
    Nakamura A, Kuru S, Hineno A, Kobayashi C, Kinoshita T, Miyazaki D, Ikeda S.
    Neurobiol Aging; 2014 Oct 31; 35(10):2420.e7-2420.e12. PubMed ID: 24838187
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