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1
Clinical and biochemical findings in ten patients with benign myalgic encephalomyelitis.10例良性肌痛性脑脊髓炎患者的临床及生化检查结果
Postgrad Med J. 1979 Dec;55(654):856-7. doi: 10.1136/pgmj.55.650.856.
2
[Activity of several plasma enzymes in heart surgery conducted under conditions of extracorporeal circulation and hypothermia].
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J Cardiovasc Surg (Torino). 1973 Nov-Dec;14(6):627-31.
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引用本文的文献

1
Post-infectious disease syndrome.感染后疾病综合征
Postgrad Med J. 1988 Jul;64(753):559-67. doi: 10.1136/pgmj.64.753.559.

本文引用的文献

1
Clinical enzymology.临床酶学
J R Soc Med. 1978 Apr;71(4):241-3. doi: 10.1177/014107687807100401.
2
Potential of radioimmunoassay of myoglobin in amniotic fluid and serum in prenatal diagnosis of Duchenne muscular dystrophy.羊水和血清中肌红蛋白放射免疫测定在杜氏肌营养不良产前诊断中的应用潜力
Lancet. 1978 Dec 9;2(8102):1250-1. doi: 10.1016/s0140-6736(78)92117-7.
3
Myoglobinaemia in Duchenne muscular dystrophy patients and carriers: A new adjunct to carrier detection.
Lancet. 1978 Sep 2;2(8088):499-501. doi: 10.1016/s0140-6736(78)92221-3.

10例良性肌痛性脑脊髓炎患者的临床及生化检查结果

Clinical and biochemical findings in ten patients with benign myalgic encephalomyelitis.

作者信息

Ramsay A M, Rundle A

出版信息

Postgrad Med J. 1979 Dec;55(654):856-7. doi: 10.1136/pgmj.55.650.856.

DOI:10.1136/pgmj.55.650.856
PMID:548947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2425703/
Abstract

Ten patients in whom the clinical findings were consistent with the syndrome variously described as 'benign myalgic encephalomyelitis', 'epidemic neuromyasthenia', 'Royal Free disease' and 'Icelandic disease' were investigated for blood levels of myoglobin and various enzymes. Although there is no clinical resemblance between the two diseases, the biochemical pattern bears a close similarity to that found in Duchenne muscular dystrophy (DMD) though differing sharply in that no rise in creatinine kinase levels was found. These findings are discussed with particular reference to recent suggestions that the permeability of cell membranes may be impaired by changes in intracellular energy mechanisms.

摘要

对10名临床症状与被不同描述为“良性肌痛性脑脊髓炎”“流行性神经肌无力”“皇家自由病”和“冰岛病”综合征相符的患者进行了肌红蛋白和各种酶的血液水平检测。尽管这两种疾病在临床症状上没有相似之处,但生化模式与杜氏肌营养不良症(DMD)非常相似,不过显著不同的是未发现肌酸激酶水平升高。结合最近关于细胞内能量机制变化可能损害细胞膜通透性的观点对这些发现进行了讨论。