相似文献
1
A rapid screening test for deficiency of plasma ceruloplasmin and its value in the diagnosis of Wilson's disease.
Am J Med. 1960 Apr;28:550-4. doi: 10.1016/0002-9343(60)90149-2.
2
Studies on copper metabolism. XXIX. A critical analysis of serum copper and ceruloplasmin concentrations in normal subjects, patients with Wilson's disease and relatives of patients with Wilson's disease.
Am J Med. 1960 Apr;28:555-63. doi: 10.1016/0002-9343(60)90150-9.
3
Some aspects of the relation of ceruloplasmin to Wilson's disease.
Neurology. 1958 Apr;8(Suppl 1):44-51. doi: 10.1212/wnl.8.suppl_1.44.
4
Observations on ceruloplasmin in Wilson's disease.
J Clin Invest. 1959 Oct;38(10 Pt 1-2):1672-82. doi: 10.1172/JCI103945.
5
Caeruloplasmin in Wilson's disease.
Lancet. 1959 Dec 26;2(7113):1163-4. doi: 10.1016/s0140-6736(59)91739-8.
6
Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).
Science. 1952 Oct 31;116(3018):484-5. doi: 10.1126/science.116.3018.484.
7
Relation of ceruloplasmin and plasma copper to hepatolenticular degeneration (Wilson's disease).
Prog Neurobiol (1956). 1956;1:52-63.
8
The heterogeneity of caeruloplasmin nd the enzymatic defect in Wilson's disease.
Helv Paediatr Acta. 1960 Nov;15:424-36.
9
Molecular studies of ceruloplasmin deficiency in Wilson's disease.
J Clin Invest. 1987 Oct;80(4):1200-4. doi: 10.1172/JCI113180.
10
Caeruloplasmin as demonstrated by starch gel electrophoresis.
J Clin Pathol. 1960 Jan;13(1):69-71. doi: 10.1136/jcp.13.1.69.
引用本文的文献
1
DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.
J Clin Invest. 1961 Apr;40(4):707-15. doi: 10.1172/JCI104304.
2
A screening test for Wilson's disease and its application to psychiatric patients.
Can Med Assoc J. 1967 Jan 14;96(2):83-6.
3
The screening of hereditary metabolic defects among newborn infants.
Can Med Assoc J. 1966 Aug 6;95(6):247-51.
4
Set of simple side-room urine tests for detection of inborn errors of metabolism.
Br Med J. 1968 Jun 22;2(5607):745-9. doi: 10.1136/bmj.2.5607.745.
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