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Journal Abstract Search

122 related items for PubMed ID: 11284995

  • 1. 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; 8(2):167-72. PubMed ID: 11284995
    [Abstract] [Full Text] [Related]

  • 2. [Sporadic amyotrophic lateral sclerosis associated with Asp90Ala CuZn-superoxide dismutase mutations in Russia].
    Skvortsova VI, Limborskaia SA, Slominskiĭ PA, Levitskaia NI, Levitskiĭ GN, Shadrina MI, Kondrat'eva EA.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2000 Mar; 100(1):44-7. PubMed ID: 10666886
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  • 3. Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country.
    Khoris J, Moulard B, Briolotti V, Hayer M, Durieux A, Clavelou P, Malafosse A, Rouleau GA, Camu W.
    Eur J Neurol; 2000 Mar; 7(2):207-11. PubMed ID: 10809943
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  • 4. [Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population].
    Skvortsova VI, Limborskaia SA, Slominskiĭ PA, Levitskiĭ GN, Levitskaia NI, Shadrina MI, Kondrat'eva EA, Brusov OS, Lysko AI, Karakhan VB, Alekhin AV, Serdiuk AV.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2003 Mar; 103(11):46-52. PubMed ID: 14681966
    [Abstract] [Full Text] [Related]

  • 5. Preserved slow conducting corticomotoneuronal projections in amyotrophic lateral sclerosis with autosomal recessive D90A CuZn-superoxide dismutase mutation.
    Weber M, Eisen A, Stewart HG, Andersen PM.
    Brain; 2000 Jul; 123 ( Pt 7)():1505-15. PubMed ID: 10869061
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  • 6. Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.
    Hand CK, Mayeux-Portas V, Khoris J, Briolotti V, Clavelou P, Camu W, Rouleau GA.
    Ann Neurol; 2001 Feb; 49(2):267-71. PubMed ID: 11220750
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  • 7. Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations.
    Jacobsson J, Jonsson PA, Andersen PM, Forsgren L, Marklund SL.
    Brain; 2001 Jul; 124(Pt 7):1461-6. PubMed ID: 11408340
    [Abstract] [Full Text] [Related]

  • 8. Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.
    Luisa Conforti F, Sprovieri T, Mazzei R, Patitucci A, Ungaro C, Zoccolella S, Magariello A, Bella VL, Tessitore A, Tedeschi G, Simone IL, Majorana G, Valentino P, Citrigno L, Gabriele A, Bono F, Monsurrò MR, Muglia M, Quattrone A.
    Amyotroph Lateral Scler; 2009 Feb; 10(1):58-60. PubMed ID: 18608106
    [Abstract] [Full Text] [Related]

  • 9. D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings.
    Giannini F, Battistini S, Mancuso M, Greco G, Ricci C, Volpi N, Del Corona A, Piazza S, Siciliano G.
    Amyotroph Lateral Scler; 2010 Feb; 11(1-2):216-9. PubMed ID: 20184519
    [Abstract] [Full Text] [Related]

  • 10. Molecular analyses of the Cu/Zn superoxide dismutase gene in patients with familial amyotrophic lateral sclerosis (ALS) in Japan.
    Aoki M, Abe K, Itoyama Y.
    Cell Mol Neurobiol; 1998 Dec; 18(6):639-47. PubMed ID: 9876871
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  • 11. 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; 247(10):783-6. PubMed ID: 11127534
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  • 13. Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
    Felbecker A, Camu W, Valdmanis PN, Sperfeld AD, Waibel S, Steinbach P, Rouleau GA, Ludolph AC, Andersen PM.
    J Neurol Neurosurg Psychiatry; 2010 May; 81(5):572-7. PubMed ID: 20460594
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  • 15. Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.
    Gellera C, Castellotti B, Riggio MC, Silani V, Morandi L, Testa D, Casali C, Taroni F, Di Donato S, Zeviani M, Mariotti C.
    Neuromuscul Disord; 2001 May; 11(4):404-10. PubMed ID: 11369193
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  • 18. "True" sporadic ALS associated with a novel SOD-1 mutation.
    Alexander MD, Traynor BJ, Miller N, Corr B, Frost E, McQuaid S, Brett FM, Green A, Hardiman O.
    Ann Neurol; 2002 Nov; 52(5):680-3. PubMed ID: 12402272
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  • 20. The physiological basis of conduction slowing in ALS patients homozygous for the D90A CuZn-SOD mutation.
    Weber M, Eisen A, Stewart HG, Andersen PM, Hirota N.
    Muscle Nerve; 2001 Jan; 24(1):89-97. PubMed ID: 11150970
    [Abstract] [Full Text] [Related]

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