琥珀胆碱诱发呼吸暂停的诊断新方法。
An original approach to the diagnosis of scoline-induced apnoea.
作者信息
Fishtal A, Evans R T, Chapman C N
出版信息
J Clin Pathol. 1972 May;25(5):422-6. doi: 10.1136/jcp.25.5.422.
Abstract
A new technique is described for measuring the rate of scoline hydrolysis by plasma cholinesterase, which may prove useful in the diagnosis of scoline sensitivity. The importance of extensive family screening is emphasized and three cases possessing a silent gene are described.
摘要
本文描述了一种用于测量血浆胆碱酯酶水解司可林速率的新技术，该技术可能对司可林敏感性的诊断有用。强调了广泛进行家族筛查的重要性，并描述了三例携带沉默基因的病例。
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An original approach to the diagnosis of scoline-induced apnoea.琥珀胆碱诱发呼吸暂停的诊断新方法。
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Succinylcholine sensitivity in a Nova Scotia family.新斯科舍省一个家族中的琥珀酰胆碱敏感性
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引用本文的文献
1
Evidence for mutation being the source of the abnormal gene for plasma cholinesterase.突变是血浆胆碱酯酶异常基因来源的证据。
J Med Genet. 1974 Jun;11(2):117-20. doi: 10.1136/jmg.11.2.117.
2
Letter: Mutation as the source of the abnormal gene for plasma cholinesterase.信件：突变作为血浆胆碱酯酶异常基因的来源。
J Med Genet. 1975 Dec;12(4):429-30. doi: 10.1136/jmg.12.4.429.
本文引用的文献
1
A 'silent' pseudo-cholinesterase gene.一个“沉默”的拟胆碱酯酶基因。
Nature. 1962 Feb 10;193:561-2. doi: 10.1038/193561a0.
2
Some statistical data on atypical cholinesterase of human serum.一些关于人血清非典型胆碱酯酶的统计数据。
Ann Hum Genet. 1959 Jul;23:239-50. doi: 10.1111/j.1469-1809.1959.tb01467.x.
3
RAPID ESTIMATION OF SERUM CHOLINESTERASE ACTIVITY USING THE ASTRUP MICRO EQUIPMENT.使用阿斯屠普微量设备快速测定血清胆碱酯酶活性
J Clin Pathol. 1965 Jul;18(4):435-40. doi: 10.1136/jcp.18.4.435.
4
Differential inhibition of human serum cholinesterase with fluoride: recognition of two new phenotypes.氟化物对人血清胆碱酯酶的差异抑制作用：两种新表型的识别。
Nature. 1961 Jul 29;191:496-8. doi: 10.1038/191496a0.
5
On distribution and inheritance of atypical forms of human serum cholinesterase, as indicated by dibucaine numbers.由地布卡因值所示的人类血清胆碱酯酶非典型形式的分布与遗传
Can J Biochem Physiol. 1957 Dec;35(12):1305-20.
6
A method for the detection of atypical forms of human serum cholinesterase; determination of dibucaine numbers.一种检测人血清胆碱酯酶非典型形式的方法；地布卡因值的测定。
Can J Biochem Physiol. 1957 Jun;35(6):339-46. doi: 10.1139/y57-041.
7
Contribution of hereditary factors to the response to drugs.遗传因素对药物反应的影响。
Fed Proc. 1965 Nov-Dec;24(6):1259-65.
8
Human cholinesterase (pseudocholinesterase): genetic variants and their recognition.人类胆碱酯酶（假性胆碱酯酶）：基因变体及其识别
Br J Anaesth. 1969 Mar;41(3):235-44. doi: 10.1093/bja/41.3.235.
9
Initial experiences with the Cholinesterase Research Unit.
Br J Anaesth. 1970 Nov;42(11):1016-20. doi: 10.1093/bja/42.11.1016.
10
Genetic aspects of succinylcholine sensitivity.琥珀酰胆碱敏感性的遗传学方面。
Anesthesiology. 1970 Feb;32(2):143-50. doi: 10.1097/00000542-197002000-00012.
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