The nature of the residual arylsulfatase activity in metachromatic leukodystrophy
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. The visceral lesions of metachromatic leukodystrophy;Wolfe;Am J Pathol,1964
2. Metachromatic leukodystrophy. V. The nature and significance of low sulfatase activity: A controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy;Austin;Arch Neurol,1965
3. Arylsulfatases;Nicholls,1971
4. Recent advances in metachromatic leukodystrophy;Neuwelt;Adv Exp Med Biol,1972
5. Mucopolysaccharidosis Type VI (Maroteaux-Lamy syndrome), I. Sulfatase B deficiency in tissues;Stumpf;Am J Dis Child,1973
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2. Metachromatic Leukodystrophy: Subtype Genotype/Phenotype Correlations and Identification of Novel Missense Mutations (P148L and P191T) Causing the Juvenile-Onset Disease;Molecular Genetics and Metabolism;1999-07
3. Arylsulfatase A Pseudodeficiency: Altered Kinetic and Heat-Inactivation Properties;Genetic Testing;1997-01
4. First trimester prenatal diagnosis of metachromatic leukodystrophy on chorionic villi by ‘Immunoprecipitation—electrophoresis’;Journal of Inherited Metabolic Disease;1988-06
5. Determination of Arylsulfatase a Activity Using Pyrene Derivatives of Cerebroside Sulfate;Lipid Storage Disorders;1988
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