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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

192 related items for PubMed ID: 19685200

  • 1. Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis.
    Luigetti M, Conte A, Madia F, Marangi G, Zollino M, Mancuso I, Dileone M, Del Grande A, Di Lazzaro V, Tonali PA, Sabatelli M.
    Neurol Sci; 2009 Dec; 30(6):517-20. PubMed ID: 19685200
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  • 3. 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; 85(9):1009-11. PubMed ID: 24591457
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  • 5. 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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  • 7. 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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  • 8. 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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  • 10. 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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  • 11. 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 Dec; 11(1-2):216-9. PubMed ID: 20184519
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  • 12. 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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  • 15. 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 29; 8(2):167-72. PubMed ID: 11284995
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  • 16. A novel L67P SOD1 mutation in an Italian ALS patient.
    del Grande A, Luigetti M, Conte A, Mancuso I, Lattante S, Marangi G, Stipa G, Zollino M, Sabatelli M.
    Amyotroph Lateral Scler; 2011 Mar 29; 12(2):150-2. PubMed ID: 21247266
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  • 20. [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 29; 103(11):46-52. PubMed ID: 14681966
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