Sanadze A G
Zh Nevropatol Psikhiatr Im S S Korsakova. 1991;91(9):93-7.
Prolonged follow-up of over 5,000 patients with myasthenia and 40 patients with Lambert-Eaton myasthenic syndrome revealed 7 patients who demonstrated, at different diseases phases, either myasthenia or Lambert-Eaton type myasthenic syndrome. However, according to the totality of all the signs, the given patients' group could be attributed neither to myasthenia nor to the myasthenic syndrome. In view of this fact and on the basis of the reported data the authors draw a conclusion about the existence of a separate synaptic disease.
对5000多名重症肌无力患者和40名兰伯特-伊顿肌无力综合征患者进行的长期随访发现,有7名患者在不同疾病阶段表现出重症肌无力或兰伯特-伊顿型肌无力综合征。然而,根据所有体征的总体情况,该患者组既不能归为重症肌无力,也不能归为肌无力综合征。鉴于这一事实,并根据报告的数据,作者得出存在一种单独的突触疾病的结论。