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43. 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; 14(3):224-7. PubMed ID: 6104322 [TBL] [Abstract][Full Text] [Related]
44. [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]
45. 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]
46. [Deficiency of arylsulfatase A activity as a basis of metachromatic leucodystrophy]. Lugowska A; Tylki-Szymańska A Postepy Biochem; 1996; 42(3):284-9. PubMed ID: 9036380 [No Abstract] [Full Text] [Related]
47. A novel mutation of the arylsulfatase A gene in late-onset metachromatic leukodystrophy. Schneider A; Hasan A; Hirschel S; Wilhelm C; Kohlhase J; Falkai P; Gärtner J; Steinfeld R; Wobrock T; Degner D J Clin Psychiatry; 2009 Dec; 70(12):1724-5. PubMed ID: 20141713 [No Abstract] [Full Text] [Related]
48. Discussion: Metachromatic leukodystrophy, an unusual case with a subtle cerebroside sulfatase defect. Kihara H UCLA Forum Med Sci; 1975; (18):501-6. PubMed ID: 828 [No Abstract] [Full Text] [Related]
49. 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]
50. Novel mutations in the arylsulfatase A gene in eight Italian families with metachromatic leukodystrophy. Bertelli M; Gallo S; Buda A; Cecchin S; Fabbri A; Lapucci C; Andrighetto G; Sidoti V; Lorusso L; Pandolfo M J Clin Neurosci; 2006 May; 13(4):443-8. PubMed ID: 16678723 [TBL] [Abstract][Full Text] [Related]
51. 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]
52. [Problems in the diagnosis of metachromatic leukodystrophy by arylsulfatase-A assay in white blood cells. Genetic study of normal enzyme values in 64 mother and child pairs (author's transl)]. Harzer K; Gussmann KI Arch Psychiatr Nervenkr (1970); 1981; 229(4):291-304. PubMed ID: 6111988 [No Abstract] [Full Text] [Related]
53. The activity of arylsulfatase A and B on tyrosine O-sulfates. Fluharty AL; Stevens RL; Goldstein EB; Kihara H Biochim Biophys Acta; 1979 Feb; 566(2):321-6. PubMed ID: 33715 [TBL] [Abstract][Full Text] [Related]
54. Biochemical aspects of globoid and metachromatic leukodystrophies. Farooqui AA; Horrocks LA Neurochem Pathol; 1984; 2(3):189-218. PubMed ID: 6152665 [TBL] [Abstract][Full Text] [Related]
55. 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]
56. A simple chromogenic assay for arylsulfatase A. Lee-Vaupel M; Conzelmann E Clin Chim Acta; 1987 Apr; 164(2):171-80. PubMed ID: 2885112 [TBL] [Abstract][Full Text] [Related]