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[Leukodystrophy, Scholz' type, (metachromatic form of diffuse sclerosis) with sphinolipoidosis (cerebroside-sulfuric acid ester storage disease)].

作者信息

JATZKEWITZ H

出版信息

Hoppe Seylers Z Physiol Chem. 1960 May 31;318:265-77. doi: 10.1515/bchm2.1960.318.1.265.

DOI:10.1515/bchm2.1960.318.1.265
PMID:14406904
Abstract
摘要

相似文献

1
[Leukodystrophy, Scholz' type, (metachromatic form of diffuse sclerosis) with sphinolipoidosis (cerebroside-sulfuric acid ester storage disease)].[舒尔茨型脑白质营养不良（弥漫性硬化的异染性形式）伴鞘脂沉积症（脑苷脂 - 硫酸酯贮积病）]
Hoppe Seylers Z Physiol Chem. 1960 May 31;318:265-77. doi: 10.1515/bchm2.1960.318.1.265.
2
[The sulfuric acid esters of cerebron and kerasin as storage substances in leukodystrophy of the Scholz type (metachromatic form of diffuse sclerosis)].[作为肖尔茨型脑白质营养不良（弥漫性硬化的异染性形式）中储存物质的脑硫脂和神经节苷脂硫酸酯]
Hoppe Seylers Z Physiol Chem. 1960 Aug 31;320:134-48. doi: 10.1515/bchm2.1960.320.1.134.
3
[Two types of cerebroside sulfates as so-called prelipids and storage substances in leukodystrophy of type Scholz (metachromatic form of diffuse sclerosis)].[两种脑硫脂作为所谓的前脂和施尔茨型脑白质营养不良（弥漫性硬化的异染性形式）中的储存物质]
Hoppe Seylers Z Physiol Chem. 1958;311(4-6):279-82.
4
Studies on adult metachromatic leukodystrophy. 2. Biochemical aspects of adult cases of metachromatic leukodystrophy.成人异染性脑白质营养不良的研究。2. 成人异染性脑白质营养不良病例的生化方面
J Neurol Sci. 1969 Nov-Dec;9(3):585-95. doi: 10.1016/0022-510x(69)90096-3.
5
[Lipoidosis--with special reference to metachromatic leucodystrophy and Tay-Sachs disease].[类脂质沉积症——特别提及异染性脑白质营养不良和泰-萨克斯病]
Nihon Rinsho. 1967 Oct;25(8):1597-606.
6
Metabolic disorders of sphingolipid metabolism in man.人类鞘脂代谢的代谢紊乱。
Chem Phys Lipids. 1970 Oct;5(1):261-9. doi: 10.1016/0009-3084(70)90023-x.
7
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 (MLD).弥漫性脑硬化的异染性形式。五、低硫酸酯酶活性的性质和意义：对四名异染性脑白质营养不良（MLD）患者的脑、肝和肾的对照研究。
Arch Neurol. 1965 Dec;13(6):593-614. doi: 10.1001/archneur.1965.00470060029003.
8
Metachromatic leucodystrophy-a generalized lipidosis. Determination of sulfatides in urine, blood plasma and cerebrospinal fluid.
Acta Paediatr (Stockh). 1960 Nov;49:690-4. doi: 10.1111/j.1651-2227.1960.tb16074.x.
9
Infantile metachromatic leukodystrophy. (Greenfield's disease).
J Neuropathol Exp Neurol. 1960 Jul;19:323-41. doi: 10.1097/00005072-196007000-00001.
10
The enzymic degradation of cerebrosides and sulphatides in human demyelination due to disseminated sclerosis and encephalitis, and to Tay-Sachs disease.由于播散性硬化症、脑炎以及泰-萨克斯病导致的人类脱髓鞘中脑苷脂和硫脂的酶促降解。
Acta Neuropathol. 1974;29(1):25-35. doi: 10.1007/BF00684388.

引用本文的文献

1
[ON THE DEGREE OF VARIATION IN PELIZAEUS-MERZBACHER DISEASE. (WITH A CONTRIBUTION TO FAMILIAL MULTIPLE SCLEROSIS)].[关于佩利措伊斯-梅茨巴赫病的变异程度。（对家族性多发性硬化症的一项贡献）]
Acta Neuropathol. 1963 Nov 5;3:87-107. doi: 10.1007/BF00687059.
2
[On a case of metachromatic leukodystrophy. A contribution to the development of teaching on leukodystrophy].[关于一例异染性脑白质营养不良症。对脑白质营养不良症教学发展的贡献]
Dtsch Z Nervenheilkd. 1963;184:213-34.
3
Ascorbic acid sulfate sulfohydrolase (C2 sulfatase): the modulator of cellular levels of L-ascorbic acid in rainbow trout.
抗坏血酸硫酸酯硫酸水解酶（C2硫酸酯酶）：虹鳟鱼中L-抗坏血酸细胞水平的调节剂。
Proc Natl Acad Sci U S A. 1982 Sep;79(18):5445-9. doi: 10.1073/pnas.79.18.5445.
4
Leucodystrophy in mink. A biochemical study.水貂的脑白质营养不良。一项生化研究。
Acta Neuropathol. 1967 Feb 3;7(4):297-304. doi: 10.1007/BF00688085.
5
Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures.异染性脑白质营养不良：皮肤成纤维细胞培养物中芳基硫酸酯酶A缺乏症。
Proc Natl Acad Sci U S A. 1969 Mar;62(3):887-91. doi: 10.1073/pnas.62.3.887.
6
Blocks in the catabolism of sulphatides and gangliosides as a cause of human neurological diseases.硫脂和神经节苷脂分解代谢受阻作为人类神经疾病的一个病因
Biochem J. 1970 Apr;117(2):6P-8P. doi: 10.1042/bj1170006p.
7
[On the storage of mucopolysaccharide-like substances in the brain in generalized glycogenosis (type II)].[关于全身性糖原贮积病（II型）中脑内类粘多糖物质的储存]
Acta Neuropathol. 1965 Jul 1;4(6):646-58. doi: 10.1007/BF00691215.