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22. Metachromatic leukodystrophy: ambiguity of heterozygote identification. Kihara H; Porter MT; Fluharty AL; Scott ML; De la Flor SD; Trammell JL; Nakamura RN Am J Ment Defic; 1973 Jan; 77(4):389-94. PubMed ID: 4706397 [No Abstract] [Full Text] [Related]
23. 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]
24. Diagnostic techniques in metachromatic leukodystrophy. Julius R; Buehler B; Aylsworth A; Petery LS; Rennert O; Greer M Neurology; 1971 Jan; 21(1):15-8. PubMed ID: 4099955 [No Abstract] [Full Text] [Related]
25. Late infantile metachromatic leucodystrophy. Report of 2 cases and review of in vivo diagnostic tests. Thunold S Beitr Pathol; 1972 Jul; 146(4):322-31. PubMed ID: 5056071 [No Abstract] [Full Text] [Related]
26. Deficiency of arylsulphatase A in leucocytes and skin fibroblasts in juvenile machromatic leucodystrophy. Leroy JG; Dumon J; Radermecker J Nature; 1970 May; 226(5245):553-4. PubMed ID: 5442355 [No Abstract] [Full Text] [Related]
30. Electron microscopic study of metachromatic leucodystrophy. 3. Lysosomal nature of the inclusions. Résibois A Acta Neuropathol; 1969; 13(2):149-56. PubMed ID: 5806784 [No Abstract] [Full Text] [Related]
32. 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]
33. 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]
34. Metachromatic leucodystrophy (sulphatide lipidoses). Juvenile type: case report. Taori GM; Mathew NT; Bhaktaviziam A; Bachhawat BK Indian J Med Res; 1969 May; 57(5):914-20. PubMed ID: 5820439 [No Abstract] [Full Text] [Related]
35. Studies on cerebral lipidosis. Enzymatic diagnosis of metachromatic leukodystrophy. Yabuuchi H; Sumi K Acta Paediatr Jpn; 1970 Dec; 12(2):1-3. PubMed ID: 4993715 [No Abstract] [Full Text] [Related]
36. 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]
39. Low sulfatase activities in metachromatic leukodystrophy (MLD). A controlled study of enzymes in 9 living and 4 autopsied patients with MLD. Austin J; McAfee D; Armstrong D; O'Rourke M; Shearer L; Bachhawat B Trans Am Neurol Assoc; 1964; 89():147-50. PubMed ID: 5828490 [No Abstract] [Full Text] [Related]
40. 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; 20(2):279-87. PubMed ID: 4698279 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]