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2. 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; 61(3):296-302. PubMed ID: 5021451 [No Abstract] [Full Text] [Related]
8. Deficiency of arylsulfatase A in juvenile metachromatic leucodystrophy: fibroblast studies. Leroy JG, Van Elsen A, Dumon JE, Radermecker J. Monogr Hum Genet; 1972 Jan; 6():148-9. PubMed ID: 4663890 [No Abstract] [Full Text] [Related]
10. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families. Pilz H. Arch Neurol; 1972 Jul; 27(1):87-90. PubMed ID: 5049684 [No Abstract] [Full Text] [Related]
12. An activator of cerebroside sulphatase in human normal liver and in cases of congenital metachromatic leukodystrophy. Jatzkewitz H, Stinshoff K. FEBS Lett; 1973 May 15; 32(1):129-31. PubMed ID: 4715673 [No Abstract] [Full Text] [Related]
13. 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 15; 20(2):279-87. PubMed ID: 4698279 [No Abstract] [Full Text] [Related]
14. Cerebroside sulfatase determination in cultured human fibroblasts. Porter MT, Fluharty AL, De la Flor SD, Kihara H. Biochim Biophys Acta; 1972 Mar 08; 258(3):769-78. PubMed ID: 5017701 [No Abstract] [Full Text] [Related]
15. The enzymic degradation of cerebrosides and sulphatides in human demyelination due to disseminated sclerosis and encephalitis, and to Tay-Sachs disease. Pellkofer R, Jatzkewitz H. Acta Neuropathol; 1974 Mar 08; 29(1):25-35. PubMed ID: 4440453 [No Abstract] [Full Text] [Related]