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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 8051919

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Sialidosis: a review of human neuraminidase deficiency.
    Lowden JA, O'Brien JS.
    Am J Hum Genet; 1979 Jan; 31(1):1-18. PubMed ID: 107795
    [No Abstract] [Full Text] [Related]

  • 23. Biochemical study of sialidosis type I in a Russian family.
    Tsvetkova IV, Petushkova NA, Zolotuchina TV, Kucharenko VI, Rosenfeld EL.
    J Inherit Metab Dis; 1987 Jan; 10(1):18-23. PubMed ID: 3106711
    [Abstract] [Full Text] [Related]

  • 24. Action myoclonus induced by visually guided movement.
    Mitoma H, Uchihara T, Yokota T, Furukawa T, Tsukagoshi H.
    J Neurol; 1993 Dec; 241(2):92-5. PubMed ID: 8138831
    [Abstract] [Full Text] [Related]

  • 25. [Two siblings of galactosialidosis with marked progression of cardiac involvement during 10 years].
    Hisahara S, Fujita T, Yoshizawa K, Mizusawa H, Shoji S.
    Rinsho Shinkeigaku; 1996 Apr; 36(4):562-5. PubMed ID: 8810850
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  • 26.
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  • 27. Sialidosis type 2 in Japan. Clinical study in two siblings' cases and review of literature.
    Matsuo T, Egawa I, Okada S, Suetsugu M, Yamamoto K, Watanabe M.
    J Neurol Sci; 1983 Jan; 58(1):45-55. PubMed ID: 6405017
    [Abstract] [Full Text] [Related]

  • 28. [Sialidosis type II, infantile form. Apropos a case].
    Menau Martín G, Chabás Bergón A, López Gil JI, Fernández-Rojo F, Girós Blasco ML, González Aparicio H.
    An Esp Pediatr; 1996 Jan; 44(1):76-8. PubMed ID: 8849070
    [No Abstract] [Full Text] [Related]

  • 29. Application of a protocol for the detection of disorders of sialic acid metabolism to 124 high-risk Brazilian patients.
    Castilhos CD, Mello AS, Burin MG, Guidobono RR, Gotardo S, Giugliani R, Coelho JC.
    Am J Med Genet A; 2003 Jun 15; 119A(3):348-51. PubMed ID: 12784303
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31.
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  • 32. A longitudinal study of Taiwanese sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndrome.
    Lai SC, Chen RS, Wu Chou YH, Chang HC, Kao LY, Huang YZ, Weng YH, Chen JK, Hwu WL, Lu CS.
    Eur J Neurol; 2009 Aug 15; 16(8):912-9. PubMed ID: 19473359
    [Abstract] [Full Text] [Related]

  • 33. Normomorphic sialidosis in two female adults with severe neurologic disease and without sialyl oligosacchariduria.
    Harzer K, Cantz M, Sewell AC, Dhareshwar SS, Roggendorf W, Heckl RW, Schofer O, Thumler R, Peiffer J, Schlote W.
    Hum Genet; 1986 Nov 15; 74(3):209-14. PubMed ID: 3096875
    [Abstract] [Full Text] [Related]

  • 34. Sialidase (alpha-n-acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry-red spots and myoclonus without dementia.
    Thomas GH, Tipton RE, Ch'ien LT, Reynolds LW, Miller CS.
    Clin Genet; 1978 Apr 15; 13(4):369-79. PubMed ID: 657577
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36.
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  • 37. Severe infantile sialidosis--the characteristics of oligosaccharides isolated from the urine and the abdominal ascites.
    Nakamura Y, Takahashi Y, Yamaguchi S, Omiya S, Orii T, Yara A, Gushiken M.
    Tohoku J Exp Med; 1992 Apr 15; 166(4):407-15. PubMed ID: 1502687
    [Abstract] [Full Text] [Related]

  • 38.
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  • 39. Neuraminidase activity in the mucolipidoses (types I, II and III) and the cherry-red spot myoclonus syndrome.
    Potier M, Beauregard G, Bélisle M, Mameli L, Hong VN, Melançon SB, Dallaire L.
    Clin Chim Acta; 1979 Dec 03; 99(2):97-105. PubMed ID: 574433
    [Abstract] [Full Text] [Related]

  • 40.
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