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Journal Abstract Search

267 related items for PubMed ID: 6580647

  • 1. Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.
    Chang PL, Davidson RG.
    Proc Natl Acad Sci U S A; 1983 Dec; 80(23):7323-7. PubMed ID: 6580647
    [Abstract] [Full Text] [Related]

  • 2. Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.
    Chang PL, Davidson RG.
    Proc Natl Acad Sci U S A; 1980 Oct; 77(10):6166-70. PubMed ID: 6108562
    [Abstract] [Full Text] [Related]

  • 3. Diagnosis of pseudo-arylsulfatase A deficiency with electrophoretic techniques.
    Chang PL, Rosa NE, Varey PA, Kihara H, Kolodny EH, Davidson RG.
    Pediatr Res; 1984 Oct; 18(10):1042-5. PubMed ID: 6149515
    [Abstract] [Full Text] [Related]

  • 4. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
    Hreidarsson SJ, Thomas GH, Kihara H, Fluharty AL, Kolodny EH, Moser HW, Reynolds LW.
    Pediatr Res; 1983 Sep; 17(9):701-4. PubMed ID: 6137805
    [Abstract] [Full Text] [Related]

  • 5. Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate.
    Kolodny EH, Mumford RA.
    Adv Exp Med Biol; 1976 Sep; 68():239-51. PubMed ID: 7105
    [Abstract] [Full Text] [Related]

  • 6. Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy.
    Chang PL, Rosa NE, Davidson RG.
    Hum Genet; 1982 Sep; 61(3):231-5. PubMed ID: 7173866
    [Abstract] [Full Text] [Related]

  • 7. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays.
    Tempesta MC, Levade T, Salvayre R.
    Clin Chim Acta; 1991 Oct 31; 202(3):149-65. PubMed ID: 1687673
    [Abstract] [Full Text] [Related]

  • 8. Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophy.
    Harzer K, Recke AS.
    Humangenetik; 1975 Oct 07; 29(4):299-307. PubMed ID: 1176145
    [Abstract] [Full Text] [Related]

  • 9. Genotype assignments in a family with the pseudo arylsulfatase a deficiency trait without metachromatic leukodystrophy.
    Kihara H, Meek WE, Fluharty AL.
    Pediatr Res; 1984 Oct 07; 18(10):1021-2. PubMed ID: 6149514
    [Abstract] [Full Text] [Related]

  • 10. Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy family.
    Dubois G, Harzer K, Baumann N.
    Am J Hum Genet; 1977 Mar 07; 29(2):191-4. PubMed ID: 15452
    [Abstract] [Full Text] [Related]

  • 11. Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts.
    Kihara H, Tsay KK, Fluharty AL.
    Hum Genet; 1984 Mar 07; 66(4):300-1. PubMed ID: 6144627
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
    Kihara H, Ho CK, Fluharty AL, Tsay KK, Hartlage PL.
    Pediatr Res; 1980 Mar 07; 14(3):224-7. PubMed ID: 6104322
    [Abstract] [Full Text] [Related]

  • 13. Infantile metachromatic leukodystrophy: deficiency of arylsulfatase A in skin fibroblasts: heterozygote detection.
    Kaback M.
    Birth Defects Orig Artic Ser; 1971 Feb 07; 7(1):239. PubMed ID: 5317490
    [No Abstract] [Full Text] [Related]

  • 14. Low arylsulphatase A activity in a family without metachromatic leukodystrophy.
    Butterworth J, Broadhead DM, Keay AJ.
    Clin Genet; 1978 Oct 07; 14(4):213-8. PubMed ID: 699360
    [Abstract] [Full Text] [Related]

  • 15. DNA-based diagnosis of arylsulfatase A deficiencies as a supplement to enzyme assay: a case in point.
    Coulter-Mackie MB, Applegarth DA, Toone J, Vallance H.
    Clin Biochem; 1997 Feb 07; 30(1):57-61. PubMed ID: 9056111
    [Abstract] [Full Text] [Related]

  • 16. 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 07; 80(19):6066-70. PubMed ID: 6136972
    [Abstract] [Full Text] [Related]

  • 17.
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  • 18. Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis.
    Basner R, von Figura K, Glössl J, Klein U, Kresse H, Mlekusch W.
    Pediatr Res; 1979 Dec 07; 13(12):1316-8. PubMed ID: 523191
    [Abstract] [Full Text] [Related]

  • 19. The nature of the residual arylsulfatase activity in metachromatic leukodystrophy.
    Shapira E, Nadler HL.
    J Pediatr; 1975 Jun 07; 86(6):881-4. PubMed ID: 1127527
    [No Abstract] [Full Text] [Related]

  • 20. Metachromatic leukodystrophy without arylsulfatase A deficiency.
    Shapiro LJ, Aleck KA, Kaback MM, Itabashi H, Desnick RJ, Brand N, Stevens RL, Fluharty AL, Kihara H.
    Pediatr Res; 1979 Oct 07; 13(10):1179-81. PubMed ID: 41211
    [Abstract] [Full Text] [Related]

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