Sitnikov V F, Khrennikov V Iu, Teselkin Iu O
Zh Nevropatol Psikhiatr Im S S Korsakova. 1987;87(3):376-81.
The authors studied the parameters of osmotic resistance and deformability of erythrocytes in patients with Duchenne's, Bekker's, Erb-Roth's and Landouzy-Déjérine's progressive muscular dystrophies, with Charcot-Marie's spinal amyotrophy, Kugelberg-Welander neural amyotrophy and with Thomsen's myotonia. Along with an increase in the erythrocytic osmotic resistance and deformability patients with different forms of hereditary neuromuscular diseases showed decreased plasma chemiluminescence (PCL) as well as an elevated ability of the blood plasma to inhibit PCL in the model chemiluminescence system in patients with Duchenne's progressive muscular dystrophy and in their close relatives.
作者研究了杜兴氏、贝克氏、埃尔布 - 罗斯氏和兰杜齐 - 德热里纳氏进行性肌营养不良症患者、夏科 - 马里氏脊髓性肌萎缩症患者、库格尔贝格 - 韦兰德氏神经源性肌萎缩症患者以及汤姆森氏肌强直患者红细胞的抗渗透和变形性参数。不同形式遗传性神经肌肉疾病患者红细胞的抗渗透和变形性增加的同时，血浆化学发光（PCL）降低，并且在杜兴氏进行性肌营养不良症患者及其近亲的模型化学发光系统中，血浆抑制PCL的能力升高。
