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Journal Abstract Search

133 related items for PubMed ID: 8051919

  • 1. Sialidosis type I: first report in the Czech population of two siblings with cherry-red spot myoclonus syndrome but without sialyloligosacchariduria.
    Ledvinová J, Poupĕtová H, Elleder M, Tichý J, Pĕnicková V, Harzer K.
    J Inherit Metab Dis; 1994; 17(1):118-9. PubMed ID: 8051919
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  • 5. Neuraminidase activities in sialidosis and mucolipidosis.
    Kuriyama M, Miyatake T, Owada M, Kitagawa T.
    J Neurol Sci; 1982 May; 54(2):181-7. PubMed ID: 7097297
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  • 7. Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobility of some enzymes known to be glycoproteins. II. Enzymes studies.
    Swallow DM, Evans L, Stewart G, Thomas PK, Abrams JD.
    Ann Hum Genet; 1979 Jul; 43(1):27-35. PubMed ID: 496393
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  • 10. The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency.
    O'Brien JS.
    Clin Genet; 1978 Jul; 14(1):55-60. PubMed ID: 679523
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  • 13. Cherry-red spot-myoclonus syndrome.
    Sogg RL, Steinman L, Rathjen B, Tharp BR, O'Brien JS, Kenyon KR.
    Ophthalmology; 1979 Oct; 86(10):1861-74. PubMed ID: 553258
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  • 18. Activated sialidase activity in transformed lymphocytes by Epstein-Barr (EB) virus of sialidosis type I (cherry-red spot-myoclonus syndrome).
    Yamamoto M, Yamauchi T, Yamamoto K, Kobayashi T.
    J Neurol Sci; 1995 Jul; 131(1):105-7. PubMed ID: 7561940
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  • 19. Juvenile galactosialidosis with attacks of neuropathic pain and absence of sialyloligosacchariduria.
    Darin N, Kyllerman M, Hård AL, Nordborg C, Månsson JE.
    Eur J Paediatr Neurol; 2009 Nov; 13(6):553-5. PubMed ID: 19097920
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