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Copper metabolism in normal adults and in clinically normal relatives of patients with Wilson's disease.

作者信息

NEALE F C, FISCHER-WILLIAMS M

出版信息

J Clin Pathol. 1958 Sep;11(5):441-7. doi: 10.1136/jcp.11.5.441.

DOI:10.1136/jcp.11.5.441
PMID:13575563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC479814/
Abstract
摘要

相似文献

1
Copper metabolism in normal adults and in clinically normal relatives of patients with Wilson's disease.正常成年人及威尔逊病患者临床正常亲属的铜代谢
J Clin Pathol. 1958 Sep;11(5):441-7. doi: 10.1136/jcp.11.5.441.
2
A critical evaluation of copper metabolism in Indian Wilson's disease children with special reference to their phenotypes and relatives.对印度威尔逊病患儿铜代谢的批判性评估，特别参考其表型和亲属情况。
Biol Trace Elem Res. 1998 Nov;65(2):153-65. doi: 10.1007/BF02784267.
3
[Occurrence of copper metabolism abnormalities in the families of four individuals with newly diagnosed Wilson's disease].[四名新诊断为威尔逊病患者家庭中铜代谢异常的发生情况]
Vnitr Lek. 1997 Feb;43(2):87-90.
4
Metabolism of copper in Wilson's disease and in normal subjects; studies with Cu-64.威尔逊病和正常受试者体内铜的代谢；用铜-64进行的研究。
Am J Med. 1954 Aug;17(2):205-13. doi: 10.1016/0002-9343(54)90258-2.
5
FURTHER studies on copper in Wilson's disease.关于威尔逊氏病中铜的进一步研究。
Nutr Rev. 1955 Aug;13(8):232-4. doi: 10.1111/j.1753-4887.1955.tb03501.x.
6
[Copper level and metallothionein-like Cu-binding protein in cultured skin fibroblasts from patients with Menkes' disease and Wilson's disease].[门克斯病和威尔逊病患者培养的皮肤成纤维细胞中的铜水平及金属硫蛋白样铜结合蛋白]
No To Shinkei. 1984 Nov;36(11):1063-8.
7
Copper transport and excretion in normal subjects and in patients with Laennec's cirrhosis and Wilson's disease: a study with CU64.正常受试者以及Laennec肝硬化和威尔逊病患者的铜转运与排泄：一项使用铜⁶⁴的研究
J Lab Clin Med. 1957 Feb;49(2):200-10.
8
COPPER and amino acids in Wilson's disease.威尔逊氏病中的铜与氨基酸
Nutr Rev. 1954 Jul;12(7):198-200. doi: 10.1111/j.1753-4887.1954.tb03283.x.
9
Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected members.使用稳定同位素65Cu检测对一个有两名患病成员的家庭进行威尔逊病筛查。
Ital J Gastroenterol Hepatol. 1998 Jun;30(3):270-5.
10
Effect of estrogens on copper metabolism in Wilson's disease.雌激素对威尔逊氏病铜代谢的影响。
J Clin Invest. 1961 Mar;40(3):445-53. doi: 10.1172/JCI104272.

引用本文的文献

1
Wilson's Disease-Genetic Puzzles with Diagnostic Implications.威尔逊氏病——具有诊断意义的遗传谜题
Diagnostics (Basel). 2023 Mar 29;13(7):1287. doi: 10.3390/diagnostics13071287.
2
Middle-aged heterozygous carriers of Wilson's disease do not present with significant phenotypic deviations related to copper metabolism.中年威尔逊病杂合子携带者未出现与铜代谢相关的明显表型偏差。
J Genet. 2010 Dec;89(4):463-7. doi: 10.1007/s12041-010-0065-3.
3
A family study of the biochemical defects in Wilson's disease.威尔逊氏病生化缺陷的家族研究。
J Clin Pathol. 1961 May;14(3):264-70. doi: 10.1136/jcp.14.3.264.
4
DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.威尔逊病基因杂合携带者的检测
J Clin Invest. 1961 Apr;40(4):707-15. doi: 10.1172/JCI104304.
5
[Advances in the recognition of heterozygous characteristics in hereditary enzymopathies].[遗传性酶病杂合子特征识别的进展]
Klin Wochenschr. 1962 Jun 1;40:553-8. doi: 10.1007/BF01478627.
6
[Serum copper in late pregnancy toxicoses].[晚期妊娠中毒症中的血清铜]
Arch Gynakol. 1960;194:158-64. doi: 10.1007/BF00668949.

本文引用的文献

1
Micro-determination of copper in biological material.生物材料中铜的微量测定。
Biochem J. 1940 Sep;34(8-9):1202-8. doi: 10.1042/bj0341202.
2
The familial nature of the amino-aciduria of Wilson's disease (hepatolenticular degeneration).威尔逊氏病（肝豆状核变性）氨基酸尿症的家族性本质。
Am J Med Sci. 1952 Apr;223(4):392-400. doi: 10.1097/00000441-195204000-00006.
3
Oxidase reactions in human plasma caused by coeruloplasmin.由铜蓝蛋白引起的人血浆中的氧化酶反应。
Scand J Clin Lab Invest. 1951;3(2):103-7. doi: 10.3109/00365515109060581.
4
A clinical and biochemical study of hepatolenticular degeneration (Wilson's disease).肝豆状核变性（威尔逊病）的临床与生化研究
Q J Med. 1957 Oct;26(104):527-58.
5
Studies on copper metabolism. XI. Copper and iron metabolism in the nephrotic syndrome.铜代谢研究。XI. 肾病综合征中的铜与铁代谢
J Clin Invest. 1954 Apr;33(4):685-98. doi: 10.1172/JCI102939.
6
Abnormalities of copper metabolism in Wilson's disease and their relationship to the aminoaciduria.威尔逊病中铜代谢异常及其与氨基酸尿症的关系。
J Clin Invest. 1954 Mar;33(3):400-9. doi: 10.1172/JCI102912.
7
Genetic and biochemical aspects of Wilson's disease.威尔逊氏病的遗传和生化方面
Am J Med. 1953 Oct;15(4):442-9. doi: 10.1016/0002-9343(53)90134-x.
8
Studies on copper metabolism. VI. Blood copper in normal human subjects.铜代谢研究。VI. 正常人体受试者的血铜
J Clin Invest. 1953 Apr;32(4):322-8. doi: 10.1172/JCI102742.
9
Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).肝豆状核变性（威尔逊病）患者血浆铜蓝蛋白缺乏。
Science. 1952 Oct 31;116(3018):484-5. doi: 10.1126/science.116.3018.484.