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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

74 related items for PubMed ID: 16443201

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  • 2. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
    García-Redondo A, Bustos F, Juan Y Seva B, Del Hoyo P, Jiménez S, Campos Y, Martín MA, Rubio JC, Cañadillas F, Arenas J, Esteban J.
    Muscle Nerve; 2002 Aug; 26(2):274-8. PubMed ID: 12210393
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  • 4. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
    Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, Cairns NJ, Kwong LK, Forman MS, Ravits J, Stewart H, Eisen A, McClusky L, Kretzschmar HA, Monoranu CM, Highley JR, Kirby J, Siddique T, Shaw PJ, Lee VM, Trojanowski JQ.
    Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
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  • 8. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
    Tan CF, Eguchi H, Tagawa A, Onodera O, Iwasaki T, Tsujino A, Nishizawa M, Kakita A, Takahashi H.
    Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220
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  • 9. The IVS1 +319 t>a of SOD1 gene is not an ALS causing mutation.
    Restagno G, Gomez A, Lombardo F, Cocco E, Calvo A, Ghiglione P, Mutani R, Chiò A.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Mar; 6(1):45-9. PubMed ID: 16036425
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  • 13. Cerebrospinal fluid neurofilament light levels in amyotrophic lateral sclerosis: impact of SOD1 genotype.
    Zetterberg H, Jacobsson J, Rosengren L, Blennow K, Andersen PM.
    Eur J Neurol; 2007 Dec; 14(12):1329-33. PubMed ID: 17903209
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  • 14. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
    Kato S, Funakoshi H, Nakamura T, Kato M, Nakano I, Hirano A, Ohama E.
    Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786
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  • 15. VCP mutations in familial and sporadic amyotrophic lateral sclerosis.
    Koppers M, van Blitterswijk MM, Vlam L, Rowicka PA, van Vught PW, Groen EJ, Spliet WG, Engelen-Lee J, Schelhaas HJ, de Visser M, van der Kooi AJ, van der Pol WL, Pasterkamp RJ, Veldink JH, van den Berg LH.
    Neurobiol Aging; 2012 Apr; 33(4):837.e7-13. PubMed ID: 22078486
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  • 16. Genetics of amyotrophic lateral sclerosis.
    Robberecht W.
    J Neurol; 2000 Dec; 247 Suppl 6():VI/2-6. PubMed ID: 19714405
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  • 17. Genetics of amyotrophic lateral sclerosis.
    Robberecht W.
    J Neurol; 2000 Dec; 247():2-6. PubMed ID: 11200702
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  • 18. Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3.
    Yamamoto-Watanabe Y, Watanabe M, Jackson M, Akimoto H, Sugimoto K, Yasujima M, Wakasaya Y, Matsubara E, Kawarabayashi T, Harigaya Y, Lyndon AR, Shoji M.
    Brain Res; 2010 Nov 18; 1361():140-5. PubMed ID: 20849835
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