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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 8599)

  • 1. Apparent biochemical homozygosity in two obligatory heterozygotes for metachromatic leukodystrophy.
    Lott IT; Dulaney JT; Milunsky A; Hoefnagel D; Moser HW
    J Pediatr; 1976 Sep; 89(3):438-40. PubMed ID: 8599
    [No Abstract]   [Full Text] [Related]  

  • 2. Biochemical abnormalities of metachromatic leukodystrophy in an adult psychiatric population.
    Mahon-Haft H; Stone RK; Johnson R; Shah S
    Am J Psychiatry; 1981 Oct; 138(10):1372-4. PubMed ID: 6117201
    [No Abstract]   [Full Text] [Related]  

  • 3. Juvenile-onset metachromatic leukodystrophy: biochemical and electrophysiologic studies.
    Clark JR; Miller RG; Vidgoff JM
    Neurology; 1979 Mar; 29(3):346-3. PubMed ID: 36575
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Metachromatic leukodystrophy and arylsulphatase A: relations and discrepancies.
    Dubois G; Turpin JC; Baumann N
    Biomedicine; 1977 Oct; 26(5):317-9. PubMed ID: 21002
    [No Abstract]   [Full Text] [Related]  

  • 5. A Km mutant of arylsulfatase A.
    Harben AM; Krawiecki N; Marcus R; Hommes FA
    Clin Chim Acta; 1982 Nov; 125(3):351-4. PubMed ID: 6129081
    [No Abstract]   [Full Text] [Related]  

  • 6. Elevated sulfatide excretion in heterozygotes of metachromatic leukodystrophy: dependence on reduction of arylsulfatase A activity.
    Molzer B; Sundt-Heller R; Kainz-Korschinsky M; Zobel M
    Am J Med Genet; 1992 Nov; 44(4):523-6. PubMed ID: 1359786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Arylsulfatases isoenzymes in metachromatic leucodystrophy/detection of a new variant by electrophoresis improvement of quantitative assay.
    Dubois G; Turpin JC; Baumann N
    Biomedicine; 1975 Apr; 23(3):116-9. PubMed ID: 4167
    [TBL] [Abstract][Full Text] [Related]  

  • 8. P-Nitrocatechol sulfate for arylsulfatase assay: detection of metachromatic leukodystrophy variants.
    Dubois G; Turpin J; Baumann N
    Adv Exp Med Biol; 1976; 68():233-7. PubMed ID: 7104
    [No Abstract]   [Full Text] [Related]  

  • 9. Auditory evoked brainstem response and high-performance liquid chromatography sulfatide assay as early indices of metachromatic leukodystrophy.
    Brown FR; Shimizu H; McDonald JM; Moser AB; Marquis P; Chen WW; Moser HW
    Neurology; 1981 Aug; 31(8):980-5. PubMed ID: 6115337
    [No Abstract]   [Full Text] [Related]  

  • 10. Juvenile and adult metachromatic leukodystrophy: partial restoration of arylsulfatase A (cerebroside sulfatase) activity by inhibitors of thiol proteinases.
    von Figura K; Steckel F; Hasilik A
    Proc Natl Acad Sci U S A; 1983 Oct; 80(19):6066-70. PubMed ID: 6136972
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple molecular forms of arylsulfatase A in different forms of metachromatic leukodystrophy (MLD).
    Farrell DF; MacMartin MP; Clark AF
    Neurology; 1979 Jan; 29(1):16-20. PubMed ID: 34126
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Enzymic detection of metachromatic leukodystrophy patients and heterozygotes.
    Jordan TW; Casey B; Weston HJ
    N Z Med J; 1977 May; 85(587):369-72. PubMed ID: 23508
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Early manifestations of multiple sulfatase deficiency.
    Burk RD; Valle D; Thomas GH; Miller C; Moser A; Moser H; Rosenbaum KN
    J Pediatr; 1984 Apr; 104(4):574-8. PubMed ID: 6142938
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Arylsulfatases A and B in leukocytes: a comparative statistical study of late infantile and juvenile forms of metachromatic leukodystrophy and controls.
    Dubois G; Turpin JC; Georges MC; Baumann N
    Biomedicine; 1980 Feb; 33(1):2-4. PubMed ID: 6102873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy.
    Stevens RL; Fluharty AL; Kihara H; Kaback MM; Shapiro LJ; Marsh B; Sandhoff K; Fischer G
    Am J Hum Genet; 1981 Nov; 33(6):900-6. PubMed ID: 6119902
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Metachromatic leukodystrophy: clinical and enzymatic parameters.
    McKhann GM
    Neuropediatrics; 1984 Sep; 15 Suppl():4-10. PubMed ID: 6152812
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diagnostic enzyme studies in patients with metachromatic leukodystrophy, and their relatives].
    Aranka L; Ilona N; Zoltán H
    Orv Hetil; 1975 Mar; 116(9):483-8. PubMed ID: 1114007
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetic heterogeneity in metachromatic leukodystrophy.
    Kihara H
    Am J Hum Genet; 1982 Mar; 34(2):171-81. PubMed ID: 6122378
    [No Abstract]   [Full Text] [Related]  

  • 19. Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.
    Eto Y; Wiesmann UN; Carson JH; Herschkowitz NN
    Arch Neurol; 1974 Feb; 30(2):153-6. PubMed ID: 4272659
    [No Abstract]   [Full Text] [Related]  

  • 20. Brain lysosomal enzymes in generalized gangliosidosis and metachromatic leukodystrophy.
    Den Tandt WR; Hooghwinkel GJ
    Acta Neurol (Napoli); 1980 Feb; 2(1):10-4. PubMed ID: 6156575
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.