mnd
- 网络国防部;运动神经元;运动神经元疾病;国家发展部;运动神经元病
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In the MND group , the latency of positive and negative waves of TCR ( P20 / N30 ) was markedly longer than that in the normal control group , and the difference was significant .
运动神经元病组三叉神经-颈反射正波/负波的峰潜伏期(P20/N30)明显高于正常对照组,差异有显著性。
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Why Prof Hawking has lived so much longer than other MND patients remains a medical mystery , however .
但是,为什么霍金可以比其他运动神经元疾病患者多活如此之久仍是个医学谜题。
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Conclusion Early muscle electrophysiology examination may be helpful for MND diagnosis in early diagnosis .
结论早期行肌肉电生理检查有助于对MND疾病的早期确诊。
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Electrophysiological examination is an important method to diagnose ALS / MND .
神经电生理检查是诊断ALS/MND的重要检查手段。
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Conclusion : MEP and EMG have important value in diagnosis and classification of MND .
结论:mMEP结合EMG检查在MND的诊断和分型中具有重要价值。
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Etiology and mechanisms of motor neuron disease ( MND ), a nervous system degeneration disease ;
运动神经元病(MND)是一组神经系统变性病,至今病因及发病机理尚不清楚。
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Netizens would like MND to come in and tell the private developer to cut its price .
网民希望国家发展部来让私人发展商降低售价。
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Conclusion There are neuromuscular transmission dysfunction and denervation-rein-nervation phenomenon in MND patients .
结论MND存在神经肌肉接头传递功能障碍和失神经&神经再支配现象;
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The prognosis of MND is poor .
MND的预后普遍较差。
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Analysis of MUP from these patients showed that the giant potential was uncommon in patients with ALS / MND .
对该组患者MUP分析表明巨大电位在ALS/MND患者肌肉中并不常见。
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Objective To elucidate the features of segmental motor nerve conduction studies in a large sample of motor neuron disease ( MND ) .
目的探讨运动神经元病(Motorneurondisease,MND)常规节段运动神经传导和位移技术检测的特点。
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Patients that had been diagnosed as motor neuron diseases ( MND ) by neurologists were reexamined .
对以往诊断为运动神经元疾病(MND)的24例患者做了重新检查。
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The cruise training commander was Admiral Lee Jay , the Chairman of Chief General Staffs , MND now .
当年的支队长为李杰将军,也就是现任的总司令;
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Objective To evaluate the diagnostic value of single-fiber electromyography ( SFEMG ) in motor neuron diseases ( MND ) .
目的探讨单纤维肌电图检测运动神经元病(MND)的临床意义。
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The disease is also known as Lou Gehrig 's Disease in the United States and motor neuron disease , or MND , in Britain .
这种病在美国称路格里克氏症,在英国称运动神经元病,或MND。
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Objective To investigate the curative effect of autologous bone marrow nuclear cells transplantation treating motor neuron disease ( MND ), and to study the mechanism of this therapy .
目的观察自体骨髓有核细胞蛛网膜下腔移植治疗运动神经元病(MND)的疗效,并探讨其机制。
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Muscle electromyogram examination for sternomastoid muscle and thoracic paraspinal muscle should be taken as routine examination for early diagnosis of MND .
常规检测胸锁乳突肌、胸段脊旁肌肌电图有助于MND早期诊断。
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Methods Anti-gangliosides GM1 antibodies and anti-cephalin antibodies in serum were detected in22 patients with MND by ELISA assay .
方法用ELISA法测定了22例MND患者血清的抗神经节苷脂GM1抗体和抗脑磷脂抗体。
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Using enzyme-linked immunosorbent assays , we examined the levels of serum and CSF antibody to GM1 Ganglioside in45 patients with MND .
乔健目的分析运动神经元疾病患者血清和脑脊液中神经节苷脂(GM1)抗体的分布,研究其在MND发病过程中的作用。
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Conclusion IGF 1 system was involved in the pathogenic mechanism of MND , the lack of neurotrophic support might be one of causes in leading to degeneration of spinal motor neurons .
结论提示IGF-1系统参与了MND的发病机理,神经营养支持的缺乏是导致脊髓运动神经元变性的原因之一。
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Methods The levels of NSE and GM1 antibody in sera and CSF of30 patients with MND were analyzed with enzyme-linked immunosorbent assays ( ELISA ) .
目的通过测定运动神经元病(MND)患者血清和脑脊液(CSF)中神经元特异性烯醇化酶(NSE)和GM1抗体,初步探讨其临床意义。
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Conclusions The normal MUNE of thenar muscles decrease with the increase of age , MUNE had good reproducibility and reliability and had great value in quantative diagnosis of MND .
结论正常人大鱼际肌MUNE随年龄增大下降,MUNE有良好的重复性和可靠性,MUNE对MND的定量诊断有重要意义。
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OBJECTIVE : To sum up and analyse the relevant hypothesises of motor neuron diseases ( MND ), and synthetically discuss the mechanisms of MND to offer the reliable basis for clinical therapy .
目的:总结并分析运动神经元病的发病机制的相关学说,综合探讨运动神经元病的发病机制,从而为临床治疗上提供可靠的依据。
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Conclusions : Using MEP , EMG and NCV jointly could provide objective evi - dence of diagnosis and type of MND and differential diagnosis of MND with cervical spondylopathy .
结论:MEP、EMG和NCV联合检查,可为MND的诊断、分型与颈椎病的鉴别诊断,提供客观依据。
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Objective To establish the normal value of motor unit number estimation ( MUNE ) of thenar muscles , to study its relationship with age and test the reproducibility of the technique and its use in MND .
目的建立大鱼际肌运动单位估数(MUNE)正常值并研究与年龄的关系和该技术的重复性及其在运动神经元病(MND)中的应用。
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Results : The latency of cortical and centra motor conduction time ( CMCT ) of motor evoked potential of ( MEP ) in MND patients were longer than those of the controls .
结果:MND组mMEP皮层潜伏期和中枢运动传导时间(CMCT)均明显长于对照组;
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According to the involved area and illness course , MND can be divided into several types , but amyotrophic lateral sclerosis ( ALS ) and progressive muscular atrophy ( PMA ) are the main types .
根据病变累及部位及病程可分为许多类型,其中最主要的有肌萎缩侧索硬化(amyotrophiclateralsclerosis,ALS)和进行性脊肌萎缩症(Progressivemuscularatrophy,PMA)。
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Motor neuron disease ( MND ) is a kind of unexplained for violation of brainstem motor nerve , damage to the spinal cord anterior horn cells and pyramidal tract as the main features of chronic progressive disease variability .
运动神经元病(MotorNeuronDiseaseMND)是一种原因不明的以侵犯脑干运动神经、损害脊髓前角细胞和锥体束为主要特征的慢性进行性变异性疾病。
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Of all outpatients in neurological clinic of Qilu hospital , the ratio of ALS / MND patients is about 0.11 % , and the number of male patients is about 2 times comparing with the number of female patients . 2 .
结论:1.我院神经内科门诊ALS/MND患者的比率为0.11%,男性患者居多,是女性患者的2倍。
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Objective : To explore the values of motion evoking potential ( MEP ), electromyogram ( EMG ) and nerve conducting velocity ( NCV ) in diagnosis , differential diagnosis and typing of motor neuron dis - ease ( MND ) .
目的:探讨联合应用运动诱发电位(MEP)、肌电图(EMG)和神经传导速度(NCV)对运动神经元病(MND)的诊断和鉴别诊断及分型的价值。