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[Augmentation of bis(monoacylglycerin)phosphric acid in sphingomyelinosis (M. Niemann-Pick?)].

作者信息

Seng P N, Debuch H, Witter B, Wiedemann H R

出版信息

Hoppe Seylers Z Physiol Chem. 1971 Feb;352(2):280-8. doi: 10.1515/bchm2.1971.352.1.280.

DOI:10.1515/bchm2.1971.352.1.280
PMID:5549569
Abstract
摘要

相似文献

1
[Augmentation of bis(monoacylglycerin)phosphric acid in sphingomyelinosis (M. Niemann-Pick?)].[鞘磷脂沉积症（尼曼-皮克病？）中双（单酰甘油）磷酸的增加]
Hoppe Seylers Z Physiol Chem. 1971 Feb;352(2):280-8. doi: 10.1515/bchm2.1971.352.1.280.
2
[Niemann-Pick disease in the adult. Lipid analyses of the body organs and the brain of autopsy- resp. biopsy material from two cases].[成人尼曼-匹克病。两例尸检及活检材料中身体器官和大脑的脂质分析]
Dtsch Med Wochenschr. 1970 Sep 18;95(38):1905-10. doi: 10.1055/s-0028-1108750.
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Hepatic and splenic glycolipids in a case of Niemann-Pick disease.
Jpn J Exp Med. 1971 Jun;41(3):221-32.
4
Niemann-Pick disease in an African child.一名非洲儿童患尼曼-匹克病。
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Altered levels of tissue glycoproteins, gangliosides, glycosaminoglycans and lipids in Niemann-Pick's disease.尼曼-匹克病中组织糖蛋白、神经节苷脂、糖胺聚糖和脂质水平的改变。
Clin Chim Acta. 1973 Oct 12;48(2):173-81. doi: 10.1016/0009-8981(73)90363-x.
6
Biochemical studies in Niemann-Pick disease. I. Major sphingolipids of liver and spleen.尼曼-匹克病的生化研究。I.肝脏和脾脏中的主要鞘脂。
Biochim Biophys Acta. 1983 Jan 7;750(1):178-84. doi: 10.1016/0005-2760(83)90218-7.
7
The juvenile form of Niemann-Pick disease.尼曼-匹克病的青少年型
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8
The subacute form of Niemann-Pick disease.尼曼-匹克病的亚急性型
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9
[Contribution to the study of spleen sphingomyelin in a case of Niemann-Pick's disease].[关于尼曼-匹克病一例中脾脏鞘磷脂研究的贡献]
J Neurochem. 1966 Sep;13(9):879-83. doi: 10.1111/j.1471-4159.1966.tb05884.x.
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Adult Niemann-Pick disease: its relationship to the syndrome of the sea-blue histiocyte.成人尼曼-匹克病：其与海蓝色组织细胞综合征的关系。
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引用本文的文献

1
Niemann-pick disease type C: new aspects in a long published family - partial manifestations in heterozygotes.尼曼-匹克病C型：一个长期报道家系的新情况——杂合子的部分表现
JIMD Rep. 2014;12:25-9. doi: 10.1007/8904_2013_240. Epub 2013 Jul 3.
2
Lactosylceramide in lysosomal storage disorders: a comparative immunohistochemical and biochemical study.溶酶体贮积症中的乳糖神经酰胺：一项比较性免疫组织化学和生物化学研究。
Virchows Arch. 2005 Jul;447(1):31-44. doi: 10.1007/s00428-005-1246-y. Epub 2005 May 26.
3
Niemann-Pick disease. Analysis of liver tissue in sphingomyelinase-deficient patients.
尼曼-匹克病。鞘磷脂酶缺乏症患者肝脏组织分析。
Virchows Arch A Pathol Anat Histol. 1980;385(2):215-31. doi: 10.1007/BF00427406.
4
Bis-(monoacylglyceryl)-phosphate of rat and human liver: fatty acid composition and NMR spectroscopy.大鼠和人肝脏的双（单酰甘油）磷酸酯：脂肪酸组成与核磁共振光谱
Lipids. 1973 Sep;8(9):531-3. doi: 10.1007/BF02531989.
5
Bis-(monoacylglyceryl)phosphate and acyl phosphatidylglycerol isolated from human livers of lipidosis induced by 4,4'-diethylaminoethoxyhexesterol.从由4,4'-二乙氨基乙氧基己醇诱导的脂质沉积症患者的人肝脏中分离出的双（单酰甘油）磷酸酯和酰基磷脂酰甘油。
Lipids. 1974 Apr;9(4):235-43. doi: 10.1007/BF02532199.
6
Lipids of alveolar macrophages, polymorphonuclear leukocytes, and their phagocytic vesicles.肺泡巨噬细胞、多形核白细胞及其吞噬小泡的脂质
J Clin Invest. 1972 Sep;51(9):2399-407. doi: 10.1172/JCI107052.
7
Late Niemann-Pick disease with neurovisceral storage: a classification problem.伴有神经内脏贮积的晚期尼曼-匹克病：一个分类问题。
J Clin Pathol. 1988 Jun;41(6):619-22. doi: 10.1136/jcp.41.6.619.
8
Low and moderate concentrations of lysobisphosphatidic acid in brain and liver of patients affected by some storage diseases.
Lipids. 1976 Jul;11(7):539-44. doi: 10.1007/BF02532899.
9
Lymph node excision as a simple diagnostic aid in rare lipidoses.淋巴结切除作为罕见脂质沉积症的一种简单诊断辅助手段。
Eur J Pediatr. 1978 Sep 8;129(2):99-101. doi: 10.1007/BF00442369.
10
Neurovisceral lipidosis compatible with Niemann-Pick disease type C: morphological and biochemical studies of a late infantile case and enzyme and lipid assays in a prenatal case of the same family.与C型尼曼-匹克病相符的神经内脏脂质沉积症：1例晚发性婴儿病例的形态学和生化研究以及同一家族1例产前病例的酶和脂质检测
Acta Neuropathol. 1978 Aug 7;43(1-2):97-104. doi: 10.1007/BF00685003.