Derakhshan I, Lotfi J, Abbsssioun K
Can J Neurol Sci. 1979 Feb;6(1):65-8. doi: 10.1017/s0317167100119390.
Clinical and pathological findings in two cases of degenerative progressive myoclonic epilepsy (PME) are described. The clinically difficult task of differentiating a "cerebellar" tremor from an action myoclonus is emphasized. Simultaneous electroencephalography and electrokymography was done, using capacity to ground transients for recording hand movements. This method was found useful in corroborating the cerebellar nature of the remaining disorder, after successful treatment of the myoclonic element with anticonvulsants.
描述了两例退行性进行性肌阵挛癫痫（PME）的临床和病理表现。强调了临床上区分“小脑性”震颤与动作性肌阵挛这一困难任务。同时进行了脑电图和肌动电流图检查，利用接地瞬变能力记录手部运动。在用抗惊厥药成功治疗肌阵挛成分后，发现该方法有助于证实剩余病症的小脑性质。
