These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

119 related items for PubMed ID: 5171491

  • 1. 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]

  • 2. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families.
    Pilz H.
    Arch Neurol; 1972 Jul; 27(1):87-90. PubMed ID: 5049684
    [No Abstract] [Full Text] [Related]

  • 3. [Familial metachromatic leucodystrophy--arylsulfatase A activity of leukocytes and probable carrier state].
    Nanba K, Taniguchi N.
    Nihon Shonika Gakkai Zasshi; 1970 Jun; 74(6):590-5. PubMed ID: 5465441
    [No Abstract] [Full Text] [Related]

  • 4. Studies on arylsulfatase-A activity in metachromatic leucodystrophy.
    Komiya K, Arima M.
    Paediatr Univ Tokyo; 1970 Dec; 18():99-104. PubMed ID: 5535257
    [No Abstract] [Full Text] [Related]

  • 5. Enzymatic abnormality of the carrier state in metachromatic leukodystrophy.
    Taniguchi N, Nanba I.
    Clin Chim Acta; 1970 Sep; 29(3):375-9. PubMed ID: 5496557
    [No Abstract] [Full Text] [Related]

  • 6. Metachromatic leukodystrophy: ambiguity of heterozygote identification.
    Kihara H, Porter MT, Fluharty AL, Scott ML, De la Flor SD, Trammell JL, Nakamura RN.
    Am J Ment Defic; 1973 Jan; 77(4):389-94. PubMed ID: 4706397
    [No Abstract] [Full Text] [Related]

  • 7. 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
    [No Abstract] [Full Text] [Related]

  • 8. 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
    [No Abstract] [Full Text] [Related]

  • 9. Metachromatic leucodystrophy. Two unusual cases of the late infantile form.
    Nyberg-Hansen R.
    Z Neurol; 1972 Jan 30; 203(2):145-54. PubMed ID: 4119025
    [No Abstract] [Full Text] [Related]

  • 10. Deficiency of arylsulfatase A in juvenile metachromatic leucodystrophy: fibroblast studies.
    Leroy JG, Van Elsen A, Dumon JE, Radermecker J.
    Monogr Hum Genet; 1972 Jan 30; 6():148-9. PubMed ID: 4663890
    [No Abstract] [Full Text] [Related]

  • 11. Late infantile metachromatic leucodystrophy. Effect of low vitamin A diet.
    Moosa A, Dubowitz V.
    Arch Dis Child; 1971 Jun 30; 46(247):381-3. PubMed ID: 5556636
    [No Abstract] [Full Text] [Related]

  • 12. 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
    [No Abstract] [Full Text] [Related]

  • 13. Chemical detection of metachromatic leukodystrophy in disease and carrier states.
    Hackett TN, Hackett RJ, Bray PF, Madsen JA.
    Am J Dis Child; 1971 Sep 09; 122(3):223-5. PubMed ID: 5568583
    [No Abstract] [Full Text] [Related]

  • 14. Infantile metachromatic leukodystrophy.
    Kaback MM, Howell RR.
    N Engl J Med; 1970 Jun 11; 282(24):1336-40. PubMed ID: 4192207
    [No Abstract] [Full Text] [Related]

  • 15. Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency.
    Austin JH.
    Arch Neurol; 1973 Apr 11; 28(4):258-64. PubMed ID: 4265903
    [No Abstract] [Full Text] [Related]

  • 16. Metachromatic leukodystrophy: diagnosis with samples of venous blood.
    Percy AK, Brady RO.
    Science; 1968 Aug 09; 161(3841):594-5. PubMed ID: 5668537
    [Abstract] [Full Text] [Related]

  • 17. [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]

  • 18. Metachromatic leucodystrophy. Assay of arylsulfatase activities in the urine.
    Hagberg B, Ockerman PA.
    Neuropadiatrie; 1970 Aug 30; 2(1):53-8. PubMed ID: 5538094
    [No Abstract] [Full Text] [Related]

  • 19. Metachromatic leucodystrophy in early childhood. Treatment with a diet deficient in vitamin A.
    Melchior JC, Clausen J.
    Acta Paediatr Scand; 1968 Jan 30; 57(1):2-8. PubMed ID: 5637009
    [No Abstract] [Full Text] [Related]

  • 20. Arylsulfatase A in the urine and metachromatic leukodystrophy.
    Greene H, Hug G, Schubert WK.
    J Pediatr; 1967 Nov 30; 71(5):709-11. PubMed ID: 6054756
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.