Hereditary deficiency of ferroxidase (aka caeruloplasmin).
作者信息
Logan J I
出版信息
J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):431-2. doi: 10.1136/jnnp.61.5.431.
Abstract
摘要
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Hereditary deficiency of ferroxidase (aka caeruloplasmin).亚铁氧化酶（又称铜蓝蛋白）遗传性缺乏。
J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):431-2. doi: 10.1136/jnnp.61.5.431.
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The ferroxidase activity of caeruloplasmin is reduced in haemodialysis patients.在血液透析患者中，铜蓝蛋白的铁氧化酶活性降低。
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A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: administration of fresh-frozen human plasma.一例伴有大脑铁沉积的遗传性血浆铜蓝蛋白缺乏症，与舞蹈症、痴呆、糖尿病和视网膜色素沉着相关：新鲜冷冻人血浆的应用
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Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.遗传性血浆铜蓝蛋白缺乏症、痴呆与糖尿病
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本文引用的文献
1
The effect of age on the non-haemin iron in the human brain.年龄对人脑非血红素铁的影响。
J Neurochem. 1958 Oct;3(1):41-51. doi: 10.1111/j.1471-4159.1958.tb12607.x.
2
Hereditary caeruloplasmin deficiency: clinicopathological study of a patient.遗传性血浆铜蓝蛋白缺乏症：1例患者的临床病理研究
J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):506-9. doi: 10.1136/jnnp.61.5.506.
3
A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus.遗传性铜蓝蛋白缺乏症合并糖尿病中铜蓝蛋白基因的无义突变。
Biochem Biophys Res Commun. 1995 Dec 5;217(1):89-95. doi: 10.1006/bbrc.1995.2749.
4
Antioxidant protection against organic and inorganic oxygen radicals by normal human plasma: the important primary role for iron-binding and iron-oxidising proteins.正常人血浆对有机和无机氧自由基的抗氧化保护作用：铁结合蛋白和铁氧化蛋白的重要首要作用。
Biochim Biophys Acta. 1993 Feb 13;1156(2):144-50. doi: 10.1016/0304-4165(93)90129-v.
5
The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake.酿酒酵母的FET3基因编码一种亚铁摄取所需的多铜氧化酶。
Cell. 1994 Jan 28;76(2):403-10. doi: 10.1016/0092-8674(94)90346-8.
6
Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.遗传性血浆铜蓝蛋白缺乏症、痴呆与糖尿病
QJM. 1994 Nov;87(11):663-70.
7
Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.遗传性血浆铜蓝蛋白缺乏症伴含铁血黄素沉着症：对一个日本家族的临床病理研究
Ann Neurol. 1995 May;37(5):646-56. doi: 10.1002/ana.410370515.
8
Aceruloplasminemia: molecular characterization of this disorder of iron metabolism.无铜蓝蛋白血症：这种铁代谢紊乱疾病的分子特征
Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2539-43. doi: 10.1073/pnas.92.7.2539.
9
A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.铜蓝蛋白基因突变与人类全身性含铁血黄素沉着症相关。
Nat Genet. 1995 Mar;9(3):267-72. doi: 10.1038/ng0395-267.
10
Caeruloplasmin: a multi-functional metalloprotein of vertebrate plasma.铜蓝蛋白：一种脊椎动物血浆中的多功能金属蛋白。
Ciba Found Symp. 1980;79:93-124. doi: 10.1002/9780470720622.ch6.
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