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2. 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]
3. 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; 29(2):191-4. PubMed ID: 15452 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Genetic heterogeneity in metachromatic leukodystrophy. Kihara H Am J Hum Genet; 1982 Mar; 34(2):171-81. PubMed ID: 6122378 [No Abstract] [Full Text] [Related]
8. Metachromatic leukodystrophy caused by a partial cerebroside sulfatase. Kihara H; Fluharty AL; O'Brien JS; Fish CH Clin Genet; 1982 Apr; 21(4):253-61. PubMed ID: 6125284 [TBL] [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; 18(10):1021-2. PubMed ID: 6149514 [TBL] [Abstract][Full Text] [Related]
10. Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts. Kihara H; Tsay KK; Fluharty AL Hum Genet; 1984; 66(4):300-1. PubMed ID: 6144627 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Pseudoarylsulfatase-A deficiency in the neurologically impaired patient. Farrell K; Applegarth DA; Toone JR; McLeod PM; Savage AV Can J Neurol Sci; 1985 Aug; 12(3):274-7. PubMed ID: 2864994 [TBL] [Abstract][Full Text] [Related]
14. Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy. Inui K; Emmett M; Wenger DA Proc Natl Acad Sci U S A; 1983 May; 80(10):3074-7. PubMed ID: 6134282 [TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of pseudo arylsulphatase A deficiency. Kihara H; Fluharty AL; Tsay KK; Bachman RP; Stephens JD; Ng WG Prenat Diagn; 1983 Jan; 3(1):29-34. PubMed ID: 6133271 [TBL] [Abstract][Full Text] [Related]
16. 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]