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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).

作者信息

Austin J, Armstrong D, Shearer L

出版信息

Arch Neurol. 1965 Dec;13(6):593-614. doi: 10.1001/archneur.1965.00470060029003.

DOI:10.1001/archneur.1965.00470060029003
PMID:4954756
Abstract
摘要

相似文献

1
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.
2
Low sulfatase activities in metachromatic leukodystrophy (MLD). A controlled study of enzymes in 9 living and 4 autopsied patients with MLD.
Trans Am Neurol Assoc. 1964;89:147-50.
3
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.
4
Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.婴儿异染性脑白质营养不良。产前诊断的确认。
N Engl J Med. 1973 Jun 28;288(26):1365-9. doi: 10.1056/NEJM197306282882602.
5
Cerebroside-sulphatase and arylsulphatase A deficiency in metachromatic leukodystrophy (ML).异染性脑白质营养不良（ML）中的脑苷脂硫酸酯酶和芳基硫酸酯酶A缺乏症。
J Neurochem. 1969 Jan;16(1):19-28. doi: 10.1111/j.1471-4159.1969.tb10339.x.
6
Metachromatic leukodystrophy. Treatment with arylsulfatase-A.异染性脑白质营养不良。芳基硫酸酯酶 -A治疗。
Arch Neurol. 1969 Feb;20(2):147-53. doi: 10.1001/archneur.1969.00480080047005.
7
Metachromatic leukodystrophy in the adult. A biochemical study.成人异染性脑白质营养不良。一项生化研究。
Neurology. 1972 Mar;22(3):312-20. doi: 10.1212/wnl.22.3.312.
8
METACHROMATIC FORM OF DIFFUSE CEREBRAL SCLEROSIS. IV. LOW SULFATASE ACTIVITY IN THE URINE OF NINE LIVING PATIENTS WITH METACHROMATIC LEUKODYSTROPHY (MLD).弥漫性脑硬化的异染性形式。IV. 九名存活的异染性脑白质营养不良（MLD）患者尿液中的低硫酸酯酶活性
Arch Neurol. 1965 May;12:447-55. doi: 10.1001/archneur.1965.00460290003001.
9
Metachromatic form of diffuse cerebral sclerosis. VI. A rapid test for the sulfatase A deficiency in metachromatic leukodystrophy (MLD) urine.
Arch Neurol. 1966 Mar;14(3):259-69. doi: 10.1001/archneur.1966.00470090031004.
10
The patterns of arylsulphatases A and B in human normal and metachromatic leucodystrophy tissues and their relationship to the cerebroside sulphatase activity.人正常组织和异染性脑白质营养不良组织中芳基硫酸酯酶A和B的模式及其与脑苷脂硫酸酯酶活性的关系。
J Neurochem. 1973 Feb;20(2):279-87. doi: 10.1111/j.1471-4159.1973.tb12127.x.

引用本文的文献

1
Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.多种硫酸酯酶缺乏症：一种由翻译后修饰缺陷引起的包含黏多糖贮积症、鞘脂贮积症等疾病的综合征。
Int J Mol Sci. 2020 May 13;21(10):3448. doi: 10.3390/ijms21103448.
2
An Introduction to Biochemical Genetics.生化遗传学导论
J R Coll Physicians Lond. 1967 Jan;1(2):167-176.
3
New sites of ocular involvement in late-infantile metachromatic leukodystrophy revealed by histopathologic studies.
组织病理学研究揭示晚发性婴儿型异染性脑白质营养不良眼部受累的新部位。
Graefes Arch Clin Exp Ophthalmol. 1993 Mar;231(3):187-91. doi: 10.1007/BF00920946.
4
Cervical cord compression and severe hydrocephalus in a child with Saudi variant of multiple sulfatase deficiency. Report of case.一名患有沙特型多种硫酸酯酶缺乏症儿童的颈髓受压和严重脑积水。病例报告。
Acta Neurochir (Wien). 1994;131(1-2):160-3. doi: 10.1007/BF01401468.
5
Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.多种硫酸酯酶缺乏症（粘脂硫酸酯贮积症）：体内培养的皮肤成纤维细胞中标记的硫酸化化合物降解受损。
Eur J Pediatr. 1980 Oct;135(1):85-9. doi: 10.1007/BF00445900.
6
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.
7
Metachromatic leukodystrophy in the habbanite Jews: high frequency in a genetic isolate and screening for heterozygotes.哈巴尼特犹太人中的异染性脑白质营养不良：遗传隔离群体中的高发病率及杂合子筛查
Am J Hum Genet. 1980 Sep;32(5):663-9.
8
The development of arylsulphatase in the small intestine of the rat.大鼠小肠中芳基硫酸酯酶的发育
Biochem J. 1969 Sep;114(2):343-50. doi: 10.1042/bj1140343.
9
Electron microscopic study of metachromatic leucodystrophy. 3. Lysosomal nature of the inclusions.异染性脑白质营养不良的电子显微镜研究。3. 包涵体的溶酶体性质。
Acta Neuropathol. 1969;13(2):149-56. doi: 10.1007/BF00687027.
10
Ocular correlates of inborn metabolic defects.先天性代谢缺陷的眼部相关因素。
Can Med Assoc J. 1966 Nov 19;95(21):1055-65.