Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum. Appropriate study populations must be used.
作者信息
McConville J P, Craig J J
出版信息
BMJ. 1998 Aug 15;317(7156):472; author reply 472-3.
Abstract
摘要
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本文引用的文献
1
Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control study.通过测量血清中S100蛋白诊断克雅氏病：前瞻性病例对照研究
BMJ. 1998 Feb 21;316(7131):577-82. doi: 10.1136/bmj.316.7131.577.
2
Early identification of variant Creutzfeldt-Jakob disease.变异型克雅氏病的早期识别
BMJ. 1998 Feb 21;316(7131):563-4. doi: 10.1136/bmj.316.7131.563.
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New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests.新型变异型克雅氏病：神经学特征与诊断测试
Lancet. 1997 Sep 27;350(9082):903-7. doi: 10.1016/s0140-6736(97)07472-2.
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Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy.通过扁桃体活检诊断新型变异型克雅氏病
Lancet. 1997 Jan 11;349(9045):99-100. doi: 10.1016/S0140-6736(97)24002-X.
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Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.散发性克雅氏病的诊断标准。
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Preclinical test for prion diseases.
Nature. 1996 Jun 13;381(6583):563. doi: 10.1038/381563a0.
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Diagnostic tests 2: Predictive values.诊断测试2：预测值。
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Diagnostic tests. 1: Sensitivity and specificity.诊断测试。1：敏感性和特异性。
BMJ. 1994 Jun 11;308(6943):1552. doi: 10.1136/bmj.308.6943.1552.
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Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.克雅氏病：全球发病模式以及家族性和散发性聚集的意义。
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