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Journal Abstract Search

186 related items for PubMed ID: 22272128

  • 21. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
    Ince PG, Tomkins J, Slade JY, Thatcher NM, Shaw PJ.
    J Neuropathol Exp Neurol; 1998 Oct; 57(10):895-904. PubMed ID: 9786240
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  • 23. Motor unit number estimation as a complementary test to routine electromyography in the diagnosis of amyotrophic lateral sclerosis.
    Gawel M, Zalewska E, Lipowska M, Kostera-Pruszczyk A, Szmidt-Salkowska E, Kaminska A.
    J Electromyogr Kinesiol; 2016 Feb; 26():60-5. PubMed ID: 26614440
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  • 25. Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.
    Pramatarova A, Figlewicz DA, Krizus A, Han FY, Ceballos-Picot I, Nicole A, Dib M, Meininger V, Brown RH, Rouleau GA.
    Am J Hum Genet; 1995 Mar; 56(3):592-6. PubMed ID: 7887412
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  • 27. Genetics of ALS in Italian families.
    Gellera C.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Mar; 2 Suppl 1():S43-6. PubMed ID: 11465924
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  • 29. Oxidative stress and metal content in blood and cerebrospinal fluid of amyotrophic lateral sclerosis patients with and without a Cu, Zn-superoxide dismutase mutation.
    Ihara Y, Nobukuni K, Takata H, Hayabara T.
    Neurol Res; 2005 Jan; 27(1):105-8. PubMed ID: 15829169
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  • 30. Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.
    Aguirre T, Matthijs G, Robberecht W, Tilkin P, Cassiman JJ.
    Eur J Hum Genet; 1999 Jul; 7(5):599-602. PubMed ID: 10439968
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  • 32. TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.
    Maekawa S, Leigh PN, King A, Jones E, Steele JC, Bodi I, Shaw CE, Hortobagyi T, Al-Sarraj S.
    Neuropathology; 2009 Dec; 29(6):672-83. PubMed ID: 19496940
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  • 36. HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis.
    Kawamoto Y, Ito H, Kobayashi Y, Suzuki Y, Akiguchi I, Fujimura H, Sakoda S, Kusaka H, Hirano A, Takahashi R.
    Neuropathol Appl Neurobiol; 2010 Jun; 36(4):331-44. PubMed ID: 20202124
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  • 38. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.
    Jackson M, Al-Chalabi A, Enayat ZE, Chioza B, Leigh PN, Morrison KE.
    Ann Neurol; 1997 Nov; 42(5):803-7. PubMed ID: 9392581
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  • 39. 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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