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Journal Abstract Search

119 related items for PubMed ID: 5171491

  • 21. The patterns of arylsulphatases A and B in human normal and metachromatic leucodystrophy tissues and their relationship to the cerebroside sulphatase activity.
    Harzer K, Stinshoff K, Mraz W, Jatzkewitz H.
    J Neurochem; 1973 Feb; 20(2):279-87. PubMed ID: 4698279
    [No Abstract] [Full Text] [Related]

  • 22. [Metachromatic leucodystrophy or sulfatidosis in children].
    Marchal C, Vidailhet M, Vidailhet C, Humbel R, Grignon G, Floquet J.
    Arch Fr Pediatr; 1970 Nov; 27(9):996. PubMed ID: 5510699
    [No Abstract] [Full Text] [Related]

  • 23. Diagnostic techniques in metachromatic leukodystrophy.
    Julius R, Buehler B, Aylsworth A, Petery LS, Rennert O, Greer M.
    Neurology; 1971 Jan; 21(1):15-8. PubMed ID: 4099955
    [No Abstract] [Full Text] [Related]

  • 24. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.
    Leroy JG, Van Elsen AF, Martin JJ, Dumon JE, Hulet AE, Okada S, Navarro C.
    N Engl J Med; 1973 Jun 28; 288(26):1365-9. PubMed ID: 4707419
    [No Abstract] [Full Text] [Related]

  • 25. Krabbe's globoid cell leukodystrophy: deficiency of glactocerebrosidase in serum, leukocytes, and fibroblasts.
    Suzuki Y, Suzuki K.
    Science; 1971 Jan 08; 171(3966):73-5. PubMed ID: 5538703
    [Abstract] [Full Text] [Related]

  • 26. Electron microscopic study of metachromatic leucodystrophy. 3. Lysosomal nature of the inclusions.
    Résibois A.
    Acta Neuropathol; 1969 Jan 08; 13(2):149-56. PubMed ID: 5806784
    [No Abstract] [Full Text] [Related]

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  • 29. Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures.
    Porter MT, Fluharty AL, Kihara H.
    Proc Natl Acad Sci U S A; 1969 Mar 08; 62(3):887-91. PubMed ID: 5257010
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  • 31. Cerebroside-sulphatase and arylsulphatase A deficiency in metachromatic leukodystrophy (ML).
    Jatzkewitz H, Mehl E.
    J Neurochem; 1969 Jan 08; 16(1):19-28. PubMed ID: 5776610
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  • 33. An activator of cerebroside sulphatase in human normal liver and in cases of congenital metachromatic leukodystrophy.
    Jatzkewitz H, Stinshoff K.
    FEBS Lett; 1973 May 15; 32(1):129-31. PubMed ID: 4715673
    [No Abstract] [Full Text] [Related]

  • 34. [Combination of metachromatic leucodystrophy and mucopolysaccharidosis: a disease entity (mucosulfatidosis)].
    Rampini S, Isler W, Baerlocher K, Bischoff A, Ulrich J, Plüss HJ.
    Helv Paediatr Acta; 1970 Nov 15; 25(5):436-61. PubMed ID: 4250178
    [No Abstract] [Full Text] [Related]

  • 35. Arylsulfatase A activity in human urine: quantitative studies on patients with lysosomal disorders including metachromatic leukodystrophy.
    Thomas GH, Howell RR.
    Clin Chim Acta; 1972 Jan 15; 36(1):99-103. PubMed ID: 5007723
    [No Abstract] [Full Text] [Related]

  • 36. The incidence and genetics of metachromatic leucodystrophy in northern Sweden.
    Gustavson KH, Hagberg B.
    Acta Paediatr Scand; 1971 Sep 15; 60(5):585-90. PubMed ID: 5110535
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  • 39. Qualitative and quantitative differences in sulfatase A which distinguish the different forms of classical metachromatic leukodystrophy (MLD).
    Stumpf D, Austin JH.
    Trans Am Neurol Assoc; 1970 Sep 15; 95():315-6. PubMed ID: 5514400
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