148 related articles for article (PubMed ID: 2876627)
1. Heterogeneity in late-onset metachromatic leukodystrophy. Effect of inhibitors of cysteine proteinases.
von Figura K; Steckel F; Conary J; Hasilik A; Shaw E
Am J Hum Genet; 1986 Sep; 39(3):371-82. PubMed ID: 2876627
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
Hreidarsson SJ; Thomas GH; Kihara H; Fluharty AL; Kolodny EH; Moser HW; Reynolds LW
Pediatr Res; 1983 Sep; 17(9):701-4. PubMed ID: 6137805
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. Diagnosis of pseudo-arylsulfatase A deficiency with electrophoretic techniques.
Chang PL; Rosa NE; Varey PA; Kihara H; Kolodny EH; Davidson RG
Pediatr Res; 1984 Oct; 18(10):1042-5. PubMed ID: 6149515
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Molecular basis of different forms of metachromatic leukodystrophy.
Polten A; Fluharty AL; Fluharty CB; Kappler J; von Figura K; Gieselmann V
N Engl J Med; 1991 Jan; 324(1):18-22. PubMed ID: 1670590
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.
Gieselmann V; Fluharty AL; Tønnesen T; Von Figura K
Am J Hum Genet; 1991 Aug; 49(2):407-13. PubMed ID: 1678251
[TBL] [Abstract][Full Text] [Related]
12. Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activity.
Bach G; Neufeld EF
Biochem Biophys Res Commun; 1983 Apr; 112(1):198-205. PubMed ID: 6132606
[TBL] [Abstract][Full Text] [Related]
13. Biochemical profiling to predict disease severity in metachromatic leukodystrophy.
Tan MA; Fuller M; Zabidi-Hussin ZA; Hopwood JJ; Meikle PJ
Mol Genet Metab; 2010 Feb; 99(2):142-8. PubMed ID: 19815439
[TBL] [Abstract][Full Text] [Related]
14. Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis.
Tønnesen T; Vrang C; Wiesmann UN; Christomanou H; Lou HO
Hum Genet; 1984; 67(2):170-3. PubMed ID: 6146562
[TBL] [Abstract][Full Text] [Related]
15. [Arylsulfatase A deficiency-metachromatic leukodystrophy].
Eto Y
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):749-52. PubMed ID: 2908400
[No Abstract] [Full Text] [Related]
16. 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]
17. Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.
Chang PL; Davidson RG
Proc Natl Acad Sci U S A; 1983 Dec; 80(23):7323-7. PubMed ID: 6580647
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Characterization of four arylsulfatase A missense mutations G86D, Y201C, D255H, and E312D causing metachromatic leukodystrophy.
Hermann S; Schestag F; Polten A; Kafert S; Penzien J; Zlotogora J; Baumann N; Gieselmann V
Am J Med Genet; 2000 Mar; 91(1):68-73. PubMed ID: 10751093
[TBL] [Abstract][Full Text] [Related]
20. Complex arylsulfatase A alleles causing metachromatic leukodystrophy.
Kappler J; Sommerlade HJ; von Figura K; Gieselmann V
Hum Mutat; 1994; 4(2):119-27. PubMed ID: 7981715
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]