Similar articles

• Sulphatases, lysosomes and disease.

  Roy AB. Roy AB. Aust J Exp Biol Med Sci. 1976 Apr;54(2):111-35. doi: 10.1038/icb.1976.13. Aust J Exp Biol Med Sci. 1976. PMID: 13772 No abstract available.
• Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate.

  Kolodny EH, Mumford RA. Kolodny EH, et al. Adv Exp Med Biol. 1976;68:239-51. doi: 10.1007/978-1-4684-7735-1_16. Adv Exp Med Biol. 1976. PMID: 7105
• P-Nitrocatechol sulfate for arylsulfatase assay: detection of metachromatic leukodystrophy variants.

  Dubois G, Turpin J, Baumann N. Dubois G, et al. Adv Exp Med Biol. 1976;68:233-7. doi: 10.1007/978-1-4684-7735-1_15. Adv Exp Med Biol. 1976. PMID: 7104 No abstract available.
• [Arylsulfatase deficiency and various metabolic diseases].

  Czyzewska K, Działoszyński L. Czyzewska K, et al. Pediatr Pol. 1978 Sep;53(9):1129-35. Pediatr Pol. 1978. PMID: 30935 Review. Polish. No abstract available.
• Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.

  Hall CW, Liebaers I, Di Natale P, Neufeld EF. Hall CW, et al. Methods Enzymol. 1978;50:439-56. doi: 10.1016/0076-6879(78)50048-7. Methods Enzymol. 1978. PMID: 26836 Review. No abstract available.