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2. 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]
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. 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]
5. 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]
6. 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]
7. 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]
12. 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]
13. Metachromatic leukodystrophy and arylsulphatase A: relations and discrepancies. Dubois G; Turpin JC; Baumann N Biomedicine; 1977 Oct; 26(5):317-9. PubMed ID: 21002 [No Abstract] [Full Text] [Related]
14. Metachromatic leukodystrophy and pseudoarylsulfatase A deficiency in a Danish family. Tønnesen T; Bro PV; Brøndum Nielsen K; Lykkelund C Acta Paediatr Scand; 1983 Mar; 72(2):175-8. PubMed ID: 6132516 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Problems in the clinical interpretation of arylsulfatase A deficiency. Zlotogora J; Schaap T; Bach G Am J Med Genet; 1981; 10(4):413-5. PubMed ID: 6120651 [No Abstract] [Full Text] [Related]
19. The relationship of the metachromatic leukodystrophies to neuropsychiatric disorders. Fluharty AL Mol Chem Neuropathol; 1990; 13(1-2):81-94. PubMed ID: 1982780 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]