Increased urinary excretion of chondroitin sulfate A and C in Hunter's syndrome.
作者信息
Onisawa J, Lee T Y
出版信息
Biochim Biophys Acta. 1970 Apr 14;208(1):144-7. doi: 10.1016/0304-4165(70)90058-9.
PMID:4985960
Abstract
摘要
相似文献
1
Increased urinary excretion of chondroitin sulfate A and C in Hunter's syndrome.亨特综合征中硫酸软骨素A和C的尿排泄增加。
Biochim Biophys Acta. 1970 Apr 14;208(1):144-7. doi: 10.1016/0304-4165(70)90058-9.
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Thin-layer gel filtration of urinary acid mucopolysaccharides in Hunter's syndrome and in normal individuals.亨特综合征及正常个体中尿酸黏多糖的薄层凝胶过滤
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[Mucopolysaccharide excretion in Hunter's disease].
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[Unusual findings in 2 patients with Hunter's disease].[2例亨廷顿病患者的异常发现]
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[Hunter's disease: study of a family from the plain of Paestum].
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Age differences in the pattern of urinary glycosaminoglycan excretion in normal individuals.
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Enzymatic studies of urinary chondroitin sulfates in normal and systemic connective tissue disease states.
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8
[Urinary acid mucopolysaccharide-peptide complexes in children. 2. Urinary acid mucopolysaccharide-peptide complexes in Hunter's syndrome].[儿童尿酸性黏多糖 - 肽复合物。2. 亨特综合征中的尿酸性黏多糖 - 肽复合物]
Nihon Shonika Gakkai Zasshi. 1970 Jan;74(1):137-47.
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The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 cases.I型、II型和III型黏多糖贮积症：23例患者的尿液检查结果
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Hunter's syndrome: a deficiency of L-idurono-sulfate sulfatase.亨特综合征：艾杜糖醛酸-2-硫酸酯酶缺乏症。
Biochem Biophys Res Commun. 1973 Oct 1;54(3):1125-32. doi: 10.1016/0006-291x(73)90809-7.
引用本文的文献
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Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion.通过血浆输注诱导黏多糖贮积症Ⅰ型和Ⅱ型中糖胺聚糖的降解
Proc Natl Acad Sci U S A. 1971 Feb;68(2):303-7. doi: 10.1073/pnas.68.2.303.
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