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Journal Abstract Search

122 related items for PubMed ID: 11284995

  • 21. 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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  • 22. Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation.
    Kato M, Aoki M, Ohta M, Nagai M, Ishizaki F, Nakamura S, Itoyama Y.
    Neurosci Lett; 2001 Oct 26; 312(3):165-8. PubMed ID: 11602336
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  • 25. 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 26; 47(5):1336-9. PubMed ID: 8909456
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  • 29. A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.
    Zhang H, Zhao H, Lu M, Zhang Y, Wang L, Zhang J, Ma D, Fan D.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Dec 26; 6(4):234-8. PubMed ID: 16319027
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  • 31. Mutational analysis of the Cu/Zn superoxide dismutase gene in a Catalan ALS population: should all sporadic ALS cases also be screened for SOD1?
    Gamez J, Corbera-Bellalta M, Nogales G, Raguer N, García-Arumí E, Badia-Canto M, Lladó-Carbó E, Alvarez-Sabín J.
    J Neurol Sci; 2006 Aug 15; 247(1):21-8. PubMed ID: 16674979
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  • 32. 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 15; 128(Pt 6):1323-9. PubMed ID: 15843422
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  • 33. Heterozygous D90A-SOD1 mutation in an Italian ALS patient with atypical presentation.
    Origone P, Caponnetto C, Mascolo M, Mandich P.
    Amyotroph Lateral Scler; 2009 Jun 15; 10(5-6):492. PubMed ID: 19922148
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  • 37. Differential motor neuron impairment and axonal regeneration in sporadic and familiar amyotrophic lateral sclerosis with SOD-1 mutations: lessons from neurophysiology.
    Bocci T, Pecori C, Giorli E, Briscese L, Tognazzi S, Caleo M, Sartucci F.
    Int J Mol Sci; 2011 Jun 15; 12(12):9203-15. PubMed ID: 22272128
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  • 38. Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.
    Berdyński M, Kuźma-Kozakiewicz M, Ricci C, Kubiszewska J, Millecamps S, Salachas F, Łusakowska A, Carrera P, Meininger V, Battistini S, Kwieciński H, Zekanowski C.
    Amyotroph Lateral Scler; 2012 Jan 15; 13(1):132-6. PubMed ID: 21877919
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  • 39. 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 15; 85(9):1009-11. PubMed ID: 24591457
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  • 40. A novel central motor conduction abnormality in D90A-homozygous patients with amyotrophic lateral sclerosis.
    Osei-Lah AD, Turner MR, Andersen PM, Leigh PN, Mills KR.
    Muscle Nerve; 2004 Jun 15; 29(6):790-4. PubMed ID: 15170611
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