[黏多糖贮积症Ⅲ型（Sanfilippo综合征）。进行性智力发育迟缓的一个病因] - Suppr | 超能文献

[Mucopolysaccharidosis type 3 (Sanfilippo's syndrome). A cause of progressive mental retardation].

作者信息

Börjeson M, Heinegård D, Ockerman P A

出版信息

Nord Med. 1969 May 1;81(18):567-9.

Abstract

摘要

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[Mucopolysaccharidosis type 3 (Sanfilippo's syndrome). A cause of progressive mental retardation].[黏多糖贮积症Ⅲ型（Sanfilippo综合征）。进行性智力发育迟缓的一个病因]

Nord Med. 1969 May 1;81(18):567-9.

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[Sanfilippo's disease, type 3 mucopolysaccharidosis].[桑菲利波病，3型黏多糖贮积症]

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[Sanfilippo's syndrome].[桑菲利波综合征]

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[The hepritin sulfate mucopolysaccharidosis (Sanfilippo's)].[硫酸乙酰肝素黏多糖贮积症（桑菲利波氏病）]

Verh Dtsch Ges Pathol. 1967;51:410-4.

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[Sanfilippo's syndrome].[桑菲利波综合征]

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[Anatomo-pathology and study of lipids in Hurler's and Sanfilippo's mucopolysaccharidosis].

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Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry.黏多糖贮积症的胡勒氏型和桑菲利普氏型。脑病理学与脂质化学。

Arch Pathol. 1971 May;91(5):434-43.

8

Aminosugar-containing low molecular weight acidic compounds present in urine of normal children and of patients affected by mucopolysaccharidosis type II, 3 or IV.正常儿童以及患有II型、III型或IV型黏多糖贮积症患者尿液中存在的含氨基糖的低分子量酸性化合物。

Ital J Biochem. 1974 May-Jun;23(3):183-201.

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[The mucopolysaccharidoses: modern diagnostic, etiopathogenetic and therapeutic trends. Enzymatic and ultrastructural study of a case of Sanfilippo's disease].[黏多糖贮积症：现代诊断、病因发病机制及治疗趋势。1例Sanfilippo病的酶学及超微结构研究]

Minerva Pediatr. 1972 Nov 24;24(41):2072-83.

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Pattern of urinary acid mucopolysaccharide excretion in five patients with genetic mucopolysaccharidoses.五例遗传性黏多糖贮积症患者尿酸黏多糖排泄模式

Tohoku J Exp Med. 1973 May;110(1):41-8. doi: 10.1620/tjem.110.41.

引用本文的文献

1

Storage of lipofuscin in neurons in mucopolysaccharidosis. Report on a case of Sanfilippo's syndrome with histochemical and electron-microscopic findings.黏多糖贮积症中脂褐素在神经元内的储存。关于1例具有组织化学和电子显微镜检查结果的Sanfilippo综合征病例的报告。

Acta Neuropathol. 1981;54(4):287-92. doi: 10.1007/BF00697002.