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Journal Abstract Search

118 related items for PubMed ID: 5556636

  • 1. Late infantile metachromatic leucodystrophy. Effect of low vitamin A diet.
    Moosa A, Dubowitz V.
    Arch Dis Child; 1971 Jun; 46(247):381-3. PubMed ID: 5556636
    [No Abstract] [Full Text] [Related]

  • 2. Metachromatic leucodystrophy in early childhood. Treatment with a diet deficient in vitamin A.
    Melchior JC, Clausen J.
    Acta Paediatr Scand; 1968 Jan; 57(1):2-8. PubMed ID: 5637009
    [No Abstract] [Full Text] [Related]

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  • 4. Metachromatic leucodystrophy. Assay of arylsulfatase activities in the urine.
    Hagberg B, Ockerman PA.
    Neuropadiatrie; 1970 Aug; 2(1):53-8. PubMed ID: 5538094
    [No Abstract] [Full Text] [Related]

  • 5. The biochemical differentiation between heterozygote carriers of metachromatic leucodystrophy and normal persons.
    Gabreëls F, Lamers K, Kok J, Loonen M, Lommen E.
    Neuropadiatrie; 1971 Apr; 2(4):461-9. PubMed ID: 5171491
    [No Abstract] [Full Text] [Related]

  • 6. Studies on arylsulfatase-A activity in metachromatic leucodystrophy.
    Komiya K, Arima M.
    Paediatr Univ Tokyo; 1970 Dec; 18():99-104. PubMed ID: 5535257
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  • 11. Infantile and adult-onset metachromatic leukodystrophy. Biochemical comparisons and predictive diagnosis.
    Percy AK, Kaback MM.
    N Engl J Med; 1971 Sep 30; 285(14):785-7. PubMed ID: 5567265
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  • 14. [Familial metachromatic leucodystrophy--arylsulfatase A activity of leukocytes and probable carrier state].
    Nanba K, Taniguchi N.
    Nihon Shonika Gakkai Zasshi; 1970 Jun 30; 74(6):590-5. PubMed ID: 5465441
    [No Abstract] [Full Text] [Related]

  • 15. Studies on cerebral lipidosis. Enzymatic diagnosis of metachromatic leukodystrophy.
    Yabuuchi H, Sumi K.
    Acta Paediatr Jpn; 1970 Dec 30; 12(2):1-3. PubMed ID: 4993715
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  • 16. [Diagnostic value of the determination of intraleukocytic arylsulfatase for the early detection of metachromatic leukodystrophy].
    Baumann N, Turpin JC, Castaigne P.
    Presse Med (1893); 1971 Jan 30; 79(6):244-5. PubMed ID: 5546796
    [No Abstract] [Full Text] [Related]

  • 17. A pedigree study of metachromatic leukodystrophy. Biochemical identification of the carrier state.
    Bass NH, Witmer EJ, Dreifuss FE.
    Neurology; 1970 Jan 30; 20(1):52-62. PubMed ID: 5460770
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  • 19. Infantile metachromatic leukodystrophy.
    Kaback MM, Howell RR.
    N Engl J Med; 1970 Jun 11; 282(24):1336-40. PubMed ID: 4192207
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  • 20. Deficiency of arylsulphatase A in leucocytes and skin fibroblasts in juvenile machromatic leucodystrophy.
    Leroy JG, Dumon J, Radermecker J.
    Nature; 1970 May 09; 226(5245):553-4. PubMed ID: 5442355
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