Niebrój-Dobosz I, Strumień M
Neurol Neurochir Pol. 1979 Jul-Aug;13(4):383-7.
Determinations of AMP-aminohydrolase activity were done in muscles in 34 cases of different neuromuscular diseases, and 30 subjects without skeletal muscle changes. In the group of patients Duchenne's progressive dystrophy accounted for 10 cases, the remaining patients had limb-girdle dystrophy, polymyositis, myotonia, collagen diseases, myopathies of nuclear aetiology, and neurogenic muscle disease. The highest fall in the activity of the enzyme was observed in Duchenne's dystrophy. The authors discuss the possible mechanism of development of these abnormalities.
对34例不同神经肌肉疾病患者的肌肉以及30例无骨骼肌病变的受试者进行了AMP氨基水解酶活性测定。在患者组中，杜兴氏进行性肌营养不良症占10例，其余患者患有肢带型肌营养不良症、多发性肌炎、肌强直、胶原病、核病因性肌病和神经源性肌肉疾病。在杜兴氏肌营养不良症中观察到该酶活性下降最为明显。作者讨论了这些异常情况发生的可能机制。
