肌阵挛
- 名myoclonia
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脑血管病患者中无肌阵挛症状的巨大SEP探讨
Features of giant somatosensory evoked potential in CVD patients without symptoms of myoclonus
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睡眠剥夺对青少年肌阵挛性癫痫患者皮质兴奋性的影响:经颅磁刺激和EEG的联合研究
Effects of sleep deprivation on cortical excitability in patients affected by juvenile myoclonic epilepsy : A combined transcranial magnetic stimulation and EEG study
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肌阵挛性SE、非惊厥性SE临床诊断困难,应行Video-EEG监测;
The diagnosis of myoclonic SE and nonconvulsive SE might be difficult and Video-EEG monitoring should be performed .
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Video-EEG对眼睑肌阵挛失神的诊断是必需的。
Video - EEG is necessary to diagnosis of EMA .
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特发性全面强直阵挛发作型癫~1H-MRS与DWI的初步研究以肌阵挛性癫痫为主要表现的亚急性二氯乙烷中毒1例报告
~ 1H-Magnetic Resonance Spectroscopy and Diffusion Weighted Image in Primarily Generalized Tonic-clonic Seizure Epilepsy A case report of subacute dichloroethane poisoning with myoclonus epilepsy as main clinical manifestation
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目的探讨肌阵挛癫痫伴破碎红纤维综合征(MERRF)的分子遗传学特点。
Objective To study the characteristics of molecular genetics concerning Chinese myoclonic epilepsy and ragged-red fiber disease ( MERRF ) .
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[结论]1.本文收集的9个家系中,其临床表型以FS、FS+为主要类型,还包括少数FS+伴失神发作、FS+伴肌阵挛发作、FS+伴局灶性发作以及特发性全面性癫痫。
Nine families in this study , the major clinical phenotype was FS and FS + also includes a small number of FS + and absence seizures , FS + with myoclonic seizures , FS + with focal seizures and idiopathic generalized epilepsy .
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对三个良性家族性肌阵挛癫痫(BAFME)家系中的31例存活患者的临床资料进行回顾性分析。
This paper retrospectively analyzed the clinical data of 31 survivors from three families with benign adult familial myoclonic epilepsy ( BAFME ) .
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目的:通过病例分析及文献资料复习对肌阵挛、癫痫及小脑性共济失调为核心症状的肌阵挛性小脑协调不能(即RamsayHunt综合征)进行探讨,以提高临床医师对其的认识。
AIM : To study the dyssynergia cerebellaris myoclonica ( Ramsay Hunt ) with myoclonus , epilepsia and cerebellar ataxia as major symptoms according to the analysis of cases and the review of literatures , in order to improve the cognition of clinicians on Ramsay Hunt .
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良性成人家族性肌阵挛癫痫三家系临床特点分析
Clinical characteristics of benign adult familial myoclonic epilepsy in three families
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肌阵挛性小脑协调不能:13例报告及6例文献复习
Dyssynergia cerebellaris myoclonica : 13 reports and 6 literatures to review
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癫痫患者皮质电刺激诱发的负性肌阵挛
Negative myoclonus induced by cortical electrical stimulation in epileptic patients
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丙戊酸钠能有效控制患者的肌阵挛或全身强直-阵挛发作。
Myoclonus or seizures could be controlled effectively with valproate .
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良性新生儿睡眠性肌阵挛:一个尚未认识的非癫痫状态
Benign neonatal sleep myoclonus : An under-recognized , non-epileptic condition
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伴共济失调和智力发育迟缓的常染色体隐性遗传的进行性肌阵挛性癫痫
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation
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动作性肌阵挛-肾衰综合征:一种独特的脑肾功能障碍性疾病特征
Action myoclonus renal failure syndrome : Characterization of a unique cerebro renal disorder
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肌阵挛发作起病年龄(13.1±3.4)岁;
Myoclonic seizures began at age of ( 13.1 ± 3.4 ) years .
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应用肉毒毒素A治疗腭肌阵挛性耳鸣临床分析
The Use of Botulinum Toxin A in the Treatment of Palatal Myoclonus Tinnitus
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以肌阵挛性癫痫为主要表现的亚急性二氯乙烷中毒1例报告
A case report of subacute dichloroethane poisoning with myoclonus epilepsy as main clinical manifestation
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进行性肌阵挛性癫痫(拉夫拉病)与葡聚糖:存在第3基因位点的证据
Progressive myoclonus epilepsy with polyglucosans ( Lafora disease ): Evidence for a third locus
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舒芬太尼预处理对依托咪酯所致肌阵挛的预防作用舒芬太尼与芬太尼预处理预防依托咪酯全身麻醉诱导后肌阵挛的效果比较
Comparison of pretreatment with sufentanil and fentanyl in prevention of myoclonus after application of etomidate
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方法回顾性分析我院诊治的2例眼睑肌阵挛失神患者的临床资料,并复习文献。
Methods The clinical data of two patients with eyelid myoclonia with absences were analyzed retrospectively .
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不宁腿和夜间肌阵挛的患病率分别为12.9%和12.3%。
The prevalences of restless leg syndrome and nocturnal myoclonus were 12.9 % and 12.3 % respectively .
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结论阵挛的腭部肌肉内注射肉毒毒素A是治疗腭肌阵挛性耳鸣的有效方法。
Conclusion The palatal muscles botulinium toxin A injection is an effective treatment for palatal myoclonus tinnitus .
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肌阵挛失神性癫痫
Epilepsy with myoclonic absences
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所有患者均以皮质震颤、肌阵挛伴或不伴癫痫发作为主要临床表现。
Cortical tremors and myoclonus with or without seizures were presented as main clinical manifestations in the patients .
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目的:探讨心肺复苏后肌阵挛的分类、诊断、治疗原则及预后。
Objective : To discuss the classification , diagnosis , treatment and prognosis of myoclonus after cardiopulmonary resuscitation .
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小儿时期肌阵挛运动的电生理学研究在体心脏早期后除极起源的电生理学研究
Electrophysiological Studies on Myoclonus in Childhood Electrophysiological Studies of Origin for Early Afterdepolarization Induced by Sotalol in Vivo
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方法:报道两例心肺复苏后肌阵挛病例并综合已有的文献研究。
Methods : We reported two cases of myoclonus after cardiopulmonary resuscitation , and reviewed existed literature researches .
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Ⅰ型主要表现为继发性不典型失神和负性肌阵挛发作,神经心理损伤预后不良;
Type ⅰ primarily represents ⅱ secondary atypical absences and negative myoclonus , often with poor neuropsychologic prognosis .