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Journal Abstract Search


116 related items for PubMed ID: 14681966

  • 1. [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; 103(11):46-52. PubMed ID: 14681966
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. 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 Mar; 11(1-2):216-9. PubMed ID: 20184519
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  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. [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 Oct 31; 100(1):44-7. PubMed ID: 10666886
    [Abstract] [Full Text] [Related]

  • 8. DNA sequence analysis of the conserved region around the SOD1 gene locus in recessively inherited ALS.
    Broom WJ, Johnson DV, Garber M, Andersen PM, Lennon N, Landers J, Nusbaum C, Russ C, Brown RH.
    Neurosci Lett; 2009 Sep 29; 463(1):64-9. PubMed ID: 19596401
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  • 12. Distinct cerebral lesions in sporadic and 'D90A' SOD1 ALS: studies with [11C]flumazenil PET.
    Turner MR, Hammers A, Al-Chalabi A, Shaw CE, Andersen PM, Brooks DJ, Leigh PN.
    Brain; 2005 Jun 29; 128(Pt 6):1323-9. PubMed ID: 15843422
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  • 13. 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 29; 124(Pt 7):1461-6. PubMed ID: 11408340
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  • 15. A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis.
    Mancuso M, Filosto M, Naini A, Rocchi A, Del Corona A, Sartucci F, Siciliano G, Murri L.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Dec 29; 3(4):215-8. PubMed ID: 12710511
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  • 16. The geographical and ethnic distribution of the D90A CuZn-SOD mutation in the Russian Federation.
    Andersen PM, Spitsyn VA, Makarov SV, Nilsson L, Kravchuk OI, Bychkovskaya LS, Marklund SL.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Jun 29; 2(2):63-9. PubMed ID: 11675874
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  • 17. 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 29; 47(5):1336-9. PubMed ID: 8909456
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  • 18. Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis.
    Dalla Bella E, Rigamonti A, Mantero V, Morbin M, Saccucci S, Gellera C, Mora G, Lauria G.
    J Neurol Neurosurg Psychiatry; 2014 Sep 29; 85(9):1009-11. PubMed ID: 24591457
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  • 20. Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia.
    Andersen PM, Nilsson P, Keränen ML, Forsgren L, Hägglund J, Karlsborg M, Ronnevi LO, Gredal O, Marklund SL.
    Brain; 1997 Oct 29; 120 ( Pt 10)():1723-37. PubMed ID: 9365366
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