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26. Metachromatic leukodystrophy and age: a comparative study of clinical, enzymological and ultrastructural findings. Luijten JA; Staal GE; Willemse J Clin Neurol Neurosurg; 1979; 81(4):221-33. PubMed ID: 45176 [TBL] [Abstract][Full Text] [Related]
27. Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiency. Hageman AT; Gabreëls FJ; de Jong JG; Gabreëls-Festen AA; van den Berg CJ; van Oost BA; Wevers RA Arch Neurol; 1995 Apr; 52(4):408-13. PubMed ID: 7710377 [TBL] [Abstract][Full Text] [Related]
28. Arylsulfatases A and B in leukocytes: a comparative statistical study of late infantile and juvenile forms of metachromatic leukodystrophy and controls. Dubois G; Turpin JC; Georges MC; Baumann N Biomedicine; 1980 Feb; 33(1):2-4. PubMed ID: 6102873 [TBL] [Abstract][Full Text] [Related]
29. Isolated peripheral neuropathy in atypical metachromatic leukodystrophy: a recurrent mutation. Coulter-Mackie MB; Applegarth DA; Toone JR; Gagnier L; Anzarut AR; Hendson G Can J Neurol Sci; 2002 May; 29(2):159-63. PubMed ID: 12035837 [TBL] [Abstract][Full Text] [Related]
30. The diagnostic value of sural nerve biopsy in metachromatic leucodystrophy and other conditions with low leucocyte arylsulphatase A activities. Vos AJ; Joosten EM; Gabreëls-Festen AA; Gabreëls FJ; Notermans SL; Lamers KJ Neuropediatrics; 1982 Feb; 13(1):42-6. PubMed ID: 6123090 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Clinical aspects of globoid cell and metachromatic leukodystrophies. Hagberg B Birth Defects Orig Artic Ser; 1971 Feb; 7(1):103-12. PubMed ID: 5173355 [TBL] [Abstract][Full Text] [Related]
33. Immunologic studies of arylsulfatase A in normal and metachromatic leukodystrophy liver. Shapira E; DeGregorio RR; Nadler HL Pediatr Res; 1978 Mar; 12(3):199-203. PubMed ID: 25410 [TBL] [Abstract][Full Text] [Related]
34. P-Nitrocatechol sulfate for arylsulfatase assay: detection of metachromatic leukodystrophy variants. Dubois G; Turpin J; Baumann N Adv Exp Med Biol; 1976; 68():233-7. PubMed ID: 7104 [No Abstract] [Full Text] [Related]
35. Metachromatic leukodystrophy: report of four cases. Wang PJ; Tzen QT; Hou JW; Lin MY; Wang TR; Shen YZ; Lee CY Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1988; 29(6):403-8. PubMed ID: 2908482 [No Abstract] [Full Text] [Related]
38. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays. Tempesta MC; Levade T; Salvayre R Clin Chim Acta; 1991 Oct; 202(3):149-65. PubMed ID: 1687673 [TBL] [Abstract][Full Text] [Related]
39. Juvenile and adult metachromatic leukodystrophy: partial restoration of arylsulfatase A (cerebroside sulfatase) activity by inhibitors of thiol proteinases. von Figura K; Steckel F; Hasilik A Proc Natl Acad Sci U S A; 1983 Oct; 80(19):6066-70. PubMed ID: 6136972 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]