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

112 related items for PubMed ID: 5514400

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

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

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. 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]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. 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 15; 77(4):389-94. PubMed ID: 4706397
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Primary enzyme immunoassay (PEIA): studies of the mutant enzyme in metachromatic leukodystrophy (primary enzyme immunoassay of arylsulfatase-A).
    Neuwelt E, Kohler PF, Austin J.
    Immunochemistry; 1973 Nov 15; 10(11):767-73. PubMed ID: 4128980
    [No Abstract] [Full Text] [Related]

  • 38. A pedigree study of metachromatic leukodystrophy. Biochemical identification of the carrier state.
    Bass NH, Witmer EJ, Dreifuss FE.
    Neurology; 1970 Jan 15; 20(1):52-62. PubMed ID: 5460770
    [No Abstract] [Full Text] [Related]

  • 39. Metachromatic leucodystrophy in early childhood. Treatment with a diet deficient in vitamin A.
    Melchior JC, Clausen J.
    Acta Paediatr Scand; 1968 Jan 15; 57(1):2-8. PubMed ID: 5637009
    [No Abstract] [Full Text] [Related]

  • 40. 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]

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