Multiple sulfatase deficiency with a novel biochemical presentation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF00442480.pdf
Reference28 articles.
1. Austin JH (1973) Studies in metachromatic leukodystrophy XII. Multiple sulfatase deficiency. Arch Neurol 28:258?264
2. Austin JH, Armstrong D, Shearer L (1965) Metachromatic form of diffuse cerebral sclerosis. V. The nature and significance of low sulfatase activity: a controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy. Arch Neurol 13:594?614
3. Bharucha BA, Naik G, Savliwala AS, Joshi RM, Kumta NB (1984) Siblings with the Austin variant of metachromatic leukodystrophy multiple sulfatidosis. Indian J Pediatr 51:477?480
4. Bischel M, Austin J, Kemeny H (1966) Metachromatic leukodystrophy VII. Elevated sulfated acid polysaccharide levels in urine and postmortem tissues. Arch Neurol 15:13?28
5. Blumenkrantz N, Asboe-Hansen G (1973) New method for quantitative determination of uronic acids. Anal Biochem 54:484?489
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