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

122 related items for PubMed ID: 4194292

  • 1. The accumulation of cerebroside sulfates by fibroblasts in culture from patients with late infantile metachromatic leukocystrophy.
    Porter MT, Fluharty AL, Harris SE, Kihara H.
    Arch Biochem Biophys; 1970 Jun; 138(2):646-52. PubMed ID: 4194292
    [No Abstract] [Full Text] [Related]

  • 2. Correction of abnormal cerebroside sulfate metabolism in cultured metachromatic leukodystrophy fibroblasts.
    Porter MT, Fluharty AL, Kihara H.
    Science; 1971 Jun 18; 172(3989):1263-5. PubMed ID: 5576165
    [Abstract] [Full Text] [Related]

  • 3. Correction of the defective sulfatide degradation in cultured fibroblasts from patients with metachromatic leucodystrophy.
    Wiesmann UN, Rossi EE, Herschkowitz NN.
    Acta Paediatr Scand; 1972 May 18; 61(3):296-302. PubMed ID: 5021451
    [No Abstract] [Full Text] [Related]

  • 4. Treatment of metachromatic leukodystrophy in fibroblasts by enzyme replacement.
    Wiesmann UN, Rossi EE, Herschkowitz NN.
    N Engl J Med; 1971 Mar 25; 284(12):672-3. PubMed ID: 5545612
    [No Abstract] [Full Text] [Related]

  • 5. 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 25; 20(2):279-87. PubMed ID: 4698279
    [No Abstract] [Full Text] [Related]

  • 6. A correlation of intracellular cerebroside sulfatase activity in fibroblasts with latency in metachromatic leukodystrophy.
    Porter MT, Fluharty AL, Trammell J, Kihara H.
    Biochem Biophys Res Commun; 1971 Aug 06; 44(3):660-6. PubMed ID: 5123204
    [No Abstract] [Full Text] [Related]

  • 7. [Two types of cerebroside sulfates as so-called prelipids and storage substances in leukodystrophy of type Scholz (metachromatic form of diffuse sclerosis)].
    JATZKEWITZ H.
    Hoppe Seylers Z Physiol Chem; 1958 Aug 06; 311(4-6):279-82. PubMed ID: 13598392
    [No Abstract] [Full Text] [Related]

  • 8. Cerebroside-sulphatase and arylsulphatase A deficiency in metachromatic leukodystrophy (ML).
    Jatzkewitz H, Mehl E.
    J Neurochem; 1969 Jan 06; 16(1):19-28. PubMed ID: 5776610
    [No Abstract] [Full Text] [Related]

  • 9. [Sulfatide lipoidosis in childhood].
    Hagberg B.
    Monatsschr Kinderheilkd (1902); 1967 Apr 06; 115(4):250-4. PubMed ID: 5592530
    [No Abstract] [Full Text] [Related]

  • 10. Evaluation of the metabolic defect in metachromatic leukodystrophy (MLD).
    Moser H, Moser AB, McKhann GM.
    Trans Am Neurol Assoc; 1967 Apr 06; 92():171-4. PubMed ID: 5634023
    [No Abstract] [Full Text] [Related]

  • 11. Enzymatic desulphation of cerebroside-3-sulphate by chicken brain arylsulphatase A.
    Farooqui AA, Bachawat BK.
    J Neurochem; 1973 Mar 06; 20(3):889-91. PubMed ID: 4703798
    [No Abstract] [Full Text] [Related]

  • 12. A cerebroside sulphotransferase deficiency in a human disorder of myelin.
    Bachhawat BK, Austin J, Armstrong D.
    Biochem J; 1967 Aug 06; 104(2):15contd-17c. PubMed ID: 4860468
    [No Abstract] [Full Text] [Related]

  • 13. Leucodystrophy in mink. A biochemical study.
    Andersen HA.
    Acta Neuropathol; 1967 Feb 03; 7(4):297-304. PubMed ID: 6067796
    [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. Metachromatic leukodystrophy in the adult. A biochemical study.
    Hirose G, Bass NH.
    Neurology; 1972 Mar 11; 22(3):312-20. PubMed ID: 5062266
    [No Abstract] [Full Text] [Related]

  • 16. Cerebroside 3-sulfate as a physiological substrate of arylsulfatase A.
    Mehl E, Jatzkewitz H.
    Biochim Biophys Acta; 1968 Mar 25; 151(3):619-27. PubMed ID: 5646041
    [No Abstract] [Full Text] [Related]

  • 17. Sulfate metabolism in metachromatic leukodystrophy.
    Moser HW, McKhann GM, Moser AE.
    Trans Am Neurol Assoc; 1964 Mar 25; 89():229-31. PubMed ID: 5828511
    [No Abstract] [Full Text] [Related]

  • 18. Deficiency of arylsulfatase A in juvenile metachromatic leucodystrophy: fibroblast studies.
    Leroy JG, Van Elsen A, Dumon JE, Radermecker J.
    Monogr Hum Genet; 1972 Mar 25; 6():148-9. PubMed ID: 4663890
    [No Abstract] [Full Text] [Related]

  • 19. Myelin Membrane: a molecular abnormality.
    O'Brien JS, Sampson EL.
    Science; 1965 Dec 17; 150(3703):1613-4. PubMed ID: 5866661
    [Abstract] [Full Text] [Related]

  • 20. The late form of metachromatic leukodystrophy. I. A histochemical and neurochemical study.
    Kraus-Ruppert R, Wildbolz A, Matthieu JM, Herschkowitz N.
    J Neurol Sci; 1972 Dec 17; 17(4):373-81. PubMed ID: 4117555
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.