Similar articles for PMID: 6136972

Year	Number of Results
1969	1
1971	3
1973	3
1974	5
1975	11
1976	10
1977	9
1978	13
1979	18
1980	14
1981	11
1982	10
1983	13
1984	13
1985	12
1986	7
1987	8
1988	12
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1990	8
1991	8
1992	3
1993	2
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1995	6
1996	8
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1998	8
1999	2
2000	4
2001	3
2002	5
2003	2
2004	1
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2006	1
2007	1
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2009	6
2010	3
2011	6
2013	1
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2015	1
2017	1
2019	3
2020	1
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2024	0

1

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. von Figura K, et al. Proc Natl Acad Sci U S A. 1983 Oct;80(19):6066-70. doi: 10.1073/pnas.80.19.6066. Proc Natl Acad Sci U S A. 1983. PMID: 6136972 Free PMC article.

2

Heterogeneity in late-onset metachromatic leukodystrophy. Effect of inhibitors of cysteine proteinases.

von Figura K, Steckel F, Conary J, Hasilik A, Shaw E. von Figura K, et al. Am J Hum Genet. 1986 Sep;39(3):371-82. Am J Hum Genet. 1986. PMID: 2876627 Free PMC article.

3

A Km mutant of arylsulfatase A.

Harben AM, Krawiecki N, Marcus R, Hommes FA. Harben AM, et al. Clin Chim Acta. 1982 Nov 10;125(3):351-4. doi: 10.1016/0009-8981(82)90266-2. Clin Chim Acta. 1982. PMID: 6129081 No abstract available.

4

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. Hreidarsson SJ, et al. Pediatr Res. 1983 Sep;17(9):701-4. doi: 10.1203/00006450-198309000-00001. Pediatr Res. 1983. PMID: 6137805

5

Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts.

Kihara H, Tsay KK, Fluharty AL. Kihara H, et al. Hum Genet. 1984;66(4):300-1. doi: 10.1007/BF00287632. Hum Genet. 1984. PMID: 6144627

6

Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy.

Stevens RL, Fluharty AL, Kihara H, Kaback MM, Shapiro LJ, Marsh B, Sandhoff K, Fischer G. Stevens RL, et al. Am J Hum Genet. 1981 Nov;33(6):900-6. Am J Hum Genet. 1981. PMID: 6119902 Free PMC article.

7

Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.

Chang PL, Davidson RG. Chang PL, et al. Proc Natl Acad Sci U S A. 1980 Oct;77(10):6166-70. doi: 10.1073/pnas.77.10.6166. Proc Natl Acad Sci U S A. 1980. PMID: 6108562 Free PMC article.

8

Juvenile-onset metachromatic leukodystrophy: biochemical and electrophysiologic studies.

Clark JR, Miller RG, Vidgoff JM. Clark JR, et al. Neurology. 1979 Mar;29(3):346-3. doi: 10.1212/wnl.29.3.346. Neurology. 1979. PMID: 36575

9

Multiple molecular forms of arylsulfatase A in different forms of metachromatic leukodystrophy (MLD).

Farrell DF, MacMartin MP, Clark AF. Farrell DF, et al. Neurology. 1979 Jan;29(1):16-20. doi: 10.1212/wnl.29.1.16. Neurology. 1979. PMID: 34126

10

Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.

Kihara H, Fluharty AL, O'Brien JS, Fish CH. Kihara H, et al. Clin Genet. 1982 Apr;21(4):253-61. doi: 10.1111/j.1399-0004.1982.tb00759.x. Clin Genet. 1982. PMID: 6125284

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