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Journal Abstract Search

171 related items for PubMed ID: 8592323

  • 1. Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments.
    de Belleroche J, Orrell R, King A.
    J Med Genet; 1995 Nov; 32(11):841-7. PubMed ID: 8592323
    [No Abstract] [Full Text] [Related]

  • 2. Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.
    Giess R, Holtmann B, Braga M, Grimm T, Müller-Myhsok B, Toyka KV, Sendtner M.
    Am J Hum Genet; 2002 May; 70(5):1277-86. PubMed ID: 11951178
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  • 3. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
    Tan CF, Piao YS, Hayashi S, Obata H, Umeda Y, Sato M, Fukushima T, Nakano R, Tsuji S, Takahashi H.
    Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
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  • 4. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
    Nakano R.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1546-8. PubMed ID: 8752459
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  • 5. Complex genetics of amyotrophic lateral sclerosis.
    Kunst CB.
    Am J Hum Genet; 2004 Dec; 75(6):933-47. PubMed ID: 15478096
    [No Abstract] [Full Text] [Related]

  • 6. Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees.
    Orlacchio A, Kawarai T, Massaro AM, St George-Hyslop PH, Sorbi S.
    Neurosci Lett; 2000 May 12; 285(2):83-6. PubMed ID: 10793232
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  • 7. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.
    Jaarsma D, Haasdijk ED, Grashorn JA, Hawkins R, van Duijn W, Verspaget HW, London J, Holstege JC.
    Neurobiol Dis; 2000 Dec 12; 7(6 Pt B):623-43. PubMed ID: 11114261
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  • 14. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.
    Rouleau GA, Clark AW, Rooke K, Pramatarova A, Krizus A, Suchowersky O, Julien JP, Figlewicz D.
    Ann Neurol; 1996 Jan 12; 39(1):128-31. PubMed ID: 8572658
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  • 15. N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.
    Mayeux V, Corcia P, Besson G, Jafari-Schluep HF, Briolotti V, Camu W.
    Ann Neurol; 2003 Jun 12; 53(6):815-8. PubMed ID: 12783432
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  • 16. Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded.
    Julien JP.
    Cell; 2001 Feb 23; 104(4):581-91. PubMed ID: 11239414
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  • 17. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.
    Cudkowicz ME, McKenna-Yasek D, Chen C, Hedley-Whyte ET, Brown RH.
    Ann Neurol; 1998 Jun 23; 43(6):703-10. PubMed ID: 9629839
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  • 20. [On intra-familial clinical diversities of a familial amyotrophic lateral sclerosis with a point mutation of Cu/Zn superoxide dismutase (Asn 86-Ser].
    Maeda T, Kurahashi K, Matsunaga M, Inoue K, Inoue M.
    No To Shinkei; 1997 Sep 23; 49(9):847-51. PubMed ID: 9311004
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