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5. Treatment of metachromatic leukodystrophy in fibroblasts by enzyme replacement. Wiesmann UN; Rossi EE; Herschkowitz NN N Engl J Med; 1971 Mar; 284(12):672-3. PubMed ID: 5545612 [No Abstract] [Full Text] [Related]
6. 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]
7. Infantile and adult-onset metachromatic leukodystrophy. Biochemical comparisons and predictive diagnosis. Percy AK; Kaback MM N Engl J Med; 1971 Sep; 285(14):785-7. PubMed ID: 5567265 [No Abstract] [Full Text] [Related]
8. [Diagnostic value of the determination of intraleukocytic arylsulfatase for the early detection of metachromatic leukodystrophy]. Baumann N; Turpin JC; Castaigne P Presse Med (1893); 1971 Jan; 79(6):244-5. PubMed ID: 5546796 [No Abstract] [Full Text] [Related]
9. Arylsulfatase A in the urine and metachromatic leukodystrophy. Greene H; Hug G; Schubert WK J Pediatr; 1967 Nov; 71(5):709-11. PubMed ID: 6054756 [No Abstract] [Full Text] [Related]
10. Studies on arylsulfatase-A activity in metachromatic leucodystrophy. Komiya K; Arima M Paediatr Univ Tokyo; 1970 Dec; 18():99-104. PubMed ID: 5535257 [No Abstract] [Full Text] [Related]
11. Chemical detection of metachromatic leukodystrophy in disease and carrier states. Hackett TN; Hackett RJ; Bray PF; Madsen JA Am J Dis Child; 1971 Sep; 122(3):223-5. PubMed ID: 5568583 [No Abstract] [Full Text] [Related]
12. Enzymatic abnormality of the carrier state in metachromatic leukodystrophy. Taniguchi N; Nanba I Clin Chim Acta; 1970 Sep; 29(3):375-9. PubMed ID: 5496557 [No Abstract] [Full Text] [Related]
13. Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures. Porter MT; Fluharty AL; Kihara H Proc Natl Acad Sci U S A; 1969 Mar; 62(3):887-91. PubMed ID: 5257010 [TBL] [Abstract][Full Text] [Related]
14. Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy. Rattazzi MC; Marks JS; Davidson RG Am J Hum Genet; 1973 May; 25(3):310-6. PubMed ID: 4704863 [No Abstract] [Full Text] [Related]
15. Qualitative and quantitative differences in sulfatase A which distinguish the different forms of classical metachromatic leukodystrophy (MLD). Stumpf D; Austin JH Trans Am Neurol Assoc; 1970; 95():315-6. PubMed ID: 5514400 [No Abstract] [Full Text] [Related]
16. An improved method for the determination of leukocyte arylsulfatase A and its application to the diagnosis of metachromatic leukodystrophy in homozygous and heterozygous states. Potter JL; Timmons GD; Rinehart L; Witmer EJ Clin Chim Acta; 1972 Jul; 39(2):518-23. PubMed ID: 5043787 [No Abstract] [Full Text] [Related]
18. Metachromatic leukodystrophy in the adult. A biochemical study. Hirose G; Bass NH Neurology; 1972 Mar; 22(3):312-20. PubMed ID: 5062266 [No Abstract] [Full Text] [Related]
19. Metachromatic leucodystrophy. Two unusual cases of the late infantile form. Nyberg-Hansen R Z Neurol; 1972; 203(2):145-54. PubMed ID: 4119025 [No Abstract] [Full Text] [Related]
20. Cerebroside-sulphatase and arylsulphatase A deficiency in metachromatic leukodystrophy (ML). Jatzkewitz H; Mehl E J Neurochem; 1969 Jan; 16(1):19-28. PubMed ID: 5776610 [No Abstract] [Full Text] [Related] [Next] [New Search]