The cerebral sphingolipidoses (metachromatic leucodystrophy and infantile amaurotic idiocy) as human inborn errors of metabolism.
作者信息
Jatzkewitz H
出版信息
Biochem J. 1972 Jun;128(1):6P. doi: 10.1042/bj1280006pa.
Abstract
摘要
相似文献
1
The cerebral sphingolipidoses (metachromatic leucodystrophy and infantile amaurotic idiocy) as human inborn errors of metabolism.脑性鞘脂类沉积症（异染性脑白质营养不良和婴儿黑蒙性白痴）作为人类先天性代谢缺陷。
Biochem J. 1972 Jun;128(1):6P. doi: 10.1042/bj1280006pa.
2
Biochemical and metabolic basis of familial sphingolipidoses.家族性鞘脂贮积症的生化与代谢基础
Semin Hematol. 1972 Jul;9(3):273-84.
3
[Biochemical aspects of sphingolipidosis].[鞘脂贮积症的生化方面]
Ann Biol Clin (Paris). 1972;30(6):623-35.
4
SPECULATIONS ON THE NATURE OF THE METABOLIC DEFECTS IN TAY-SACHS, NIEMANN-PICK, GAUCHER'S AND ALZHEIMER'S DISEASES, AND METACHROMATIC LEUCODYSTROPHY.关于泰-萨克斯病、尼曼-匹克病、高雪氏病、阿尔茨海默病及异染性脑白质营养不良症中代谢缺陷本质的推测
J Am Oil Chem Soc. 1965 May;42:412-6. doi: 10.1007/BF02635578.
5
[Lipoidosis--with special reference to metachromatic leucodystrophy and Tay-Sachs disease].
Nihon Rinsho. 1967 Oct;25(8):1597-606.
6
[Sphingolipidoses. Biochemistry and enzymatic mechanisms].[鞘脂贮积病。生物化学与酶促机制]
Nouv Presse Med. 1972 Jun 24;1(26):1789-92.
7
[Sphingolipidosis].[鞘脂贮积症]
Arch Fr Pediatr. 1971 Nov;28(9):909-14.
8
STUDIES ON METACHROMATIC LEUCODYSTROPHY. 2. URINE SEDIMENT EXAMINATION FOR THE DIAGNOSIS IN LIFETIME.异染性脑白质营养不良的研究。2. 用于生前诊断的尿沉渣检查
Acta Paediatr Jpn. 1964 Jun;31:16-25. doi: 10.1111/j.1442-200x.1964.tb01102.x.
9
Some aspects of the cellular biochemistry of lysosomal and related glycosidases.溶酶体及相关糖苷酶的细胞生物化学的某些方面。
Mol Cell Biochem. 1973 Dec 15;2(2):169-77. doi: 10.1007/BF01795471.
10
[Biochemical and pathological aspects of sphingolipidoses].[鞘脂贮积症的生化与病理学方面]
Bull Schweiz Akad Med Wiss. 1968 Jul;24(1):73-94.
Zotero 插件