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21. Adult metachromatic leukodystrophy. IV. Ultrastructural studies on the central and peripheral nervous system. Goebel HH; Argyrakis A; Shimokawa K; Seidel D; Heipertz R Eur Neurol; 1980; 19(5):294-307. PubMed ID: 6249606 [TBL] [Abstract][Full Text] [Related]
22. Adult metachromatic leukodystrophy without deficiency of arylsulphatase. Wang LN; Huang KW; Wang DG; Liu ZY Chin Med J (Engl); 1990 Oct; 103(10):846-50. PubMed ID: 1980099 [TBL] [Abstract][Full Text] [Related]
23. The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsy. Hahn AF; Gordon BA; Gilbert JJ; Hinton GG Acta Neuropathol; 1981; 55(4):281-7. PubMed ID: 6120612 [TBL] [Abstract][Full Text] [Related]
24. Ocular findings in metachromatic leukodystrophy. An electron microscopic and enzyme study in different clinical and genetic variants. Libert J; Van Hoof F; Toussaint D; Roozitalab H; Kenyon KR; Green WR Arch Ophthalmol; 1979 Aug; 97(8):1495-504. PubMed ID: 37822 [TBL] [Abstract][Full Text] [Related]
25. Arylsulfatase A (ASA) defect and psychiatric illness. A review. Shah SN Mol Chem Neuropathol; 1990 Mar; 12(2):121-9; discussion 143-5. PubMed ID: 1981468 [TBL] [Abstract][Full Text] [Related]
26. Metachromatic leukodystrophy: a comparative study of the ultrastructural findings in the peripheral nervous system of three cases, one of the late infantile, one of the juvenile and one of the adult form of the disease. Luijten JA; Straks W; Blikkendaal-Lieftinck LF; Staal GE; Willemse J Neuropadiatrie; 1978 Nov; 9(4):338-50. PubMed ID: 218147 [TBL] [Abstract][Full Text] [Related]
27. [Arylsulfatase deficiency and various metabolic diseases]. Czyzewska K; Działoszyński L Pediatr Pol; 1978 Sep; 53(9):1129-35. PubMed ID: 30935 [No Abstract] [Full Text] [Related]
28. Monozygotic twins with presumed metachromatic leukodystrophy. Activity of arylsulfatase A in serum of patients and family. Hashimoto T; Minato H; Kuroda Y; Toshima K; Ohara K; Miyao M Arch Neurol; 1978 Oct; 35(10):689-91. PubMed ID: 29593 [TBL] [Abstract][Full Text] [Related]
29. Comparative ultrastructural observations on peripheral nerve abnormalities in the late infantile, juvenile and late onset forms of metachromatic leukodystrophy. Thomas PK; King RH; Kocen RS; Brett EM Acta Neuropathol; 1977 Aug; 39(3):237-45. PubMed ID: 199031 [TBL] [Abstract][Full Text] [Related]
30. Lipid storage diseases: review of the cases admitted to the Istituto Neurologico. D'Angelo A; Moise A; Rimoldi M; Bertagnolio B; Ottolenghi A; Tettamanti G; Di Donato S Biochem Exp Biol; 1977; 13(1):71-8. PubMed ID: 26367 [No Abstract] [Full Text] [Related]
31. Prenatal exclusion of late infantile metachromatic leucodystrophy in a late-presenting pregnancy by assay of fetal leucocytes. Rodeck CH; Fensom AH; Benson PF; Ellis M Prenat Diagn; 1983 Jul; 3(3):257-9. PubMed ID: 6137816 [TBL] [Abstract][Full Text] [Related]
32. Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene. Marcão AM; Wiest R; Schindler K; Wiesmann U; Weis J; Schroth G; Miranda MC; Sturzenegger M; Gieselmann V Arch Neurol; 2005 Feb; 62(2):309-13. PubMed ID: 15710861 [TBL] [Abstract][Full Text] [Related]
33. Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis. Basner R; von Figura K; Glössl J; Klein U; Kresse H; Mlekusch W Pediatr Res; 1979 Dec; 13(12):1316-8. PubMed ID: 523191 [TBL] [Abstract][Full Text] [Related]
34. Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts. Chang PL; Davidson RG Proc Natl Acad Sci U S A; 1980 Oct; 77(10):6166-70. PubMed ID: 6108562 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy. Artigalás O; Lagranha VL; Saraiva-Pereira ML; Burin MG; Lourenço CM; van der Linden H; Santos ML; Rosemberg S; Steiner CE; Kok F; de Souza CF; Jardim LB; Giugliani R; Schwartz IV J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S257-62. PubMed ID: 20596894 [TBL] [Abstract][Full Text] [Related]