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: 4715673

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

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Metachromatic leukodystrophy in the adult. A biochemical study.
    Hirose G, Bass NH.
    Neurology; 1972 Mar; 22(3):312-20. PubMed ID: 5062266
    [No Abstract] [Full Text] [Related]

  • 24. The activator of cerebroside-sulphatase. A model of the activation.
    Fischer G, Jatzkewitz H.
    Biochim Biophys Acta; 1978 Jan 27; 528(1):69-76. PubMed ID: 23173
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 27. 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 27; 2(4):461-9. PubMed ID: 5171491
    [No Abstract] [Full Text] [Related]

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

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

  • 30. A preclinical case of late adult metachromatic leukodystrophy? Manifestation only with lipid abnormalities in urine, enzyme deficiency and decrease of nerve conduction velocity.
    Pilz H, Hopf HC.
    J Neurol Neurosurg Psychiatry; 1972 Jun 27; 35(3):360-4. PubMed ID: 4338447
    [Abstract] [Full Text] [Related]

  • 31. An improved method for the determination of leukocyte arylsulfatase A and its application to the diagnosis of metachromatic leukodystrophy in homozygous and heterozygous states.
    Potter JL, Timmons GD, Rinehart L, Witmer EJ.
    Clin Chim Acta; 1972 Jul 27; 39(2):518-23. PubMed ID: 5043787
    [No Abstract] [Full Text] [Related]

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

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

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Defective sulfatide synthesis in Krabbe's disease (globoid leukodystrophy).
    Austin J, Bachhawat B, Armstrong D, Stumpf D, Kretschmer L, Mitchell C, Van Zee B.
    J Neuropathol Exp Neurol; 1968 Jan 27; 27(1):141-2. PubMed ID: 5656559
    [No Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy.
    Rattazzi MC, Marks JS, Davidson RG.
    Am J Hum Genet; 1973 May 09; 25(3):310-6. PubMed ID: 4704863
    [No Abstract] [Full Text] [Related]

  • 38. 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]

  • 39. The use of white cells as a source of diagnostic material for lipid storage diseases.
    Snyder RA, Brady RO.
    Clin Chim Acta; 1969 Aug 09; 25(2):331-8. PubMed ID: 4895581
    [No Abstract] [Full Text] [Related]

  • 40. Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures.
    Porter MT, Fluharty AL, Kihara H.
    Proc Natl Acad Sci U S A; 1969 Mar 09; 62(3):887-91. PubMed ID: 5257010
    [Abstract] [Full Text] [Related]

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