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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

174 related items for PubMed ID: 7643359

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  • 2. Identification of a novel exon 4 SOD1 mutation in a sporadic amyotrophic lateral sclerosis patient.
    Jones CT, Shaw PJ, Chari G, Brock DJ.
    Mol Cell Probes; 1994 Aug; 8(4):329-30. PubMed ID: 7870076
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  • 8. Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis.
    Hosler BA, Nicholson GA, Sapp PC, Chin W, Orrell RW, de Belleroche JS, Esteban J, Hayward LJ, Mckenna-Yasek D, Yeung L, Cherryson AK, Dench JE, Wilton SD, Laing NG, Horvitz HR, Brown RH.
    Neuromuscul Disord; 1996 Oct; 6(5):361-6. PubMed ID: 8938700
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  • 11. Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis.
    Robberecht W, Sapp P, Viaene MK, Rosen D, McKenna-Yasek D, Haines J, Horvitz R, Theys P, Brown R.
    J Neurochem; 1994 Jan; 62(1):384-7. PubMed ID: 8263541
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  • 12. 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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  • 13. Identification of a novel SOD1 mutation in an apparently sporadic amyotrophic lateral sclerosis patient and the detection of Ile113Thr in three others.
    Jones CT, Swingler RJ, Brock DJ.
    Hum Mol Genet; 1994 Apr; 3(4):649-50. PubMed ID: 8069312
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  • 16. 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; 252(7):782-8. PubMed ID: 15789135
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  • 17. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.
    Jackson M, Al-Chalabi A, Enayat ZE, Chioza B, Leigh PN, Morrison KE.
    Ann Neurol; 1997 Nov; 42(5):803-7. PubMed ID: 9392581
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