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 *

197 related articles for article (PubMed ID: 15452)

  • 21. Measurement of recombinant human arylsulfatase A and leukocyte sulfatase activities by analytical isotachophoresis.
    Pajarola S; Weißenberg C; Baysal F; Bruchelt G; Krägeloh-Mann I; Böhringer J
    J Chromatogr B Analyt Technol Biomed Life Sci; 2019 Aug; 1124():109-113. PubMed ID: 31195190
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [An exceptional case of a family suffering from metachromatic leukocystrophy. Very low level of arylsulfatase A and cerebroside sulfate sulfatase in healthy subjects].
    Turpin JC; Bergondi C; Haidar H; Dubois G
    Nouv Presse Med; 1977 Apr; 6(16):1373, 1379. PubMed ID: 16245
    [No Abstract]   [Full Text] [Related]  

  • 23. Retinal pigment epithelial degeneration and arylsulfatase A deficiency.
    Zlotogora J; Schaap T; Bach G
    Am J Ophthalmol; 1981 Jul; 92(1):136-8. PubMed ID: 6114638
    [No Abstract]   [Full Text] [Related]  

  • 24. 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; 68():239-51. PubMed ID: 7105
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A variant form of metachromatic leukodystrophy without arylsulfatase deficiency.
    Hahn AF; Gordon BA; Hinton GG; Gilbert JJ
    Ann Neurol; 1982 Jul; 12(1):33-6. PubMed ID: 6126151
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Placental steroid deficiency: association with arylsulfatase A deficiency.
    Vidgoff J; Buxman MM; Shapiro LJ; Dimond RL; Wilson TG; Hepburn CA; Tabei T; Heinrichs WR
    Am J Hum Genet; 1982 May; 34(3):434-43. PubMed ID: 6123259
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Monozygotic twins with presumed metachromatic leukodystrophy. Activity of arylsulfatase A in serum of patients and family.
    Hashimoto T; Minato H; Kuroda Y; Toshima K; Ohara K; Miyao M
    Arch Neurol; 1978 Oct; 35(10):689-91. PubMed ID: 29593
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 13(10):1179-81. PubMed ID: 41211
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pseudodeficiencies in lysosomal storage disorders.
    Zlotogora J; Bach G
    Lancet; 1985 Dec; 2(8467):1296. PubMed ID: 2866352
    [No Abstract]   [Full Text] [Related]  

  • 33. Presymptomatic diagnosis: metachromatic leukodystrophy or pseudo arylsulphatase A deficiency?
    Kihara H; Fluharty AL; Ng WG; Leider W
    J Inherit Metab Dis; 1982; 5(4):215-7. PubMed ID: 6133034
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Arylsulfatase A (ASA) defect and psychiatric illness. A review.
    Shah SN
    Mol Chem Neuropathol; 1990 Mar; 12(2):121-9; discussion 143-5. PubMed ID: 1981468
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Leukocyte sulfatidase for the reliable diagnosis of metachromatic leukodystrophy.
    Raghavan SS; Gajewski A; Kolodny EH
    J Neurochem; 1981 Feb; 36(2):724-31. PubMed ID: 6109767
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Letter: Absence of ASA activity in healthy father of a patient with metachromatic leukodystrophy.
    Dubois G; Turpin JC; Baumann N
    N Engl J Med; 1975 Aug; 293(6):302. PubMed ID: 1138177
    [No Abstract]   [Full Text] [Related]  

  • 37. Adult metachromatic leukodystrophy. Arylsulphatase-A values in four generations of one family and some reflections about the genetics.
    Hoes MJ; Lamers KJ; Hommes OR; ter Haar B
    Clin Neurol Neurosurg; 1978; 80(3):174-88. PubMed ID: 34493
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Detecting MLD carriers.
    Pickett J
    Neurology; 1979 Sep; 29(9 Pt 1):1314. PubMed ID: 39274
    [No Abstract]   [Full Text] [Related]  

  • 39. Immunofluorescence staining and immunological studies of arylsulphatase A of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts.
    Tanaka A; Higami S; Isshiki G; Matsumoto T; Furusawa M
    J Inherit Metab Dis; 1983; 6(1):21-6. PubMed ID: 6134864
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Metachromatic leukodystrophy].
    Aracena M; Valenzuela E; Selman E; Milos C
    Rev Chil Pediatr; 1984; 55(6):411-3. PubMed ID: 6152638
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.