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1.Relationship of Microcirculation and Hemorheology in Motor Neuron Disease
运动神经元病微循环与血液流变学的关系收藏指正
2.RELATIONSHIP AMONG MEP,EMG,NCV AND CLINIC IN PATIEATS WITH MOTOR NEURON DISEASE
运动神经元病的MEP、EMG、NCV与临床收藏指正
3.CLINICAL OBSERVATION OF THERAPEUTIC EFFECTS OF ALLOSTERIC SNAKE NEUROTOXIN SN 114 CASES OF MOTOR NEURON DISEASE
变构蛇神经毒素治疗运动神经元病114例的临床观察收藏指正
4.Objective To investigate the diagnositic value of single fiber electromygraphy (SFEMG) in motor neuron disease (MND) and study the relationship among the abnormal SFEMG, disease type and disease severity.
目的研究单纤维肌电图（SFEMG）对运动神经元病的辅助诊断价值及探讨单纤维肌电图异常率与其病型、病情的关系。收藏指正
5.Result The 14 cases fulfilled probable or definite ALS E1 Escorial categories having upper and lower motor neuron signs.
结果依据Escorial诊断标准,14例连枷臂综合征患者均符合确诊或拟诊的肌萎缩侧索硬化。收藏指正
6.The patient was a 71 year old man who developed muscle wasting and weakness and had electromyographic evidence of motor neuron disease.
患者是71岁男性,渐发肌肉萎缩和无力,肌电图描记的证据显示为运动神经元病。收藏指正
7.Prof Hawking, who is confined to a wheelchair by motor neuron disease, MND, was commenting using a muscle below his right eye to operate - via a switch on his glasses - his voice synthesiser.
霍金教授由于运动神经元病而困坐轮椅，他用右眼下的肌肉，透过眼镜上的开关，操作他的发声合成器发表这项意见。收藏指正
8.Conclusion Neurogenic changes of EMG of rectus abdominis muscle might be regarded as an evidence of the lesion in lower motor neuron involved in thoracic region and is helpful in the diagnosis of ALS.
结论腹直肌肌电图各参数均能可靠、稳定地测出,可作为检测ALS患者胸段下运动神经元病变的辅助手段。收藏指正
9.Methods:40 ALS patients complying with the revised El Escorial criteria,8 patients with pure lower motor neuron(LMN)involvement and 34 age and sex matched healthy controls were enrolled in the study. TMS-MEP measurements were performed on bilateral abductor digiti minimi(ADM)and tibialis anterior(TA)muscles of all the subjects.
方法:对符合1998年修订的E1Escorial诊断标准的ALS患者40例、单纯下运动神经元(LMN)受累患者8例和健康对照34例进行双小指展肌、胫前肌TMS-MEP测定。收藏指正
10.The SMN d etection revealed deletion of exon 7 and exon 8 in 11 of 13 cases, only lacking exon 7 in 1 of 13 cases and lacking exon 8 in 1 of 13 cases. Conclus ion SMA is characterized by degeneration of lower motor neuron assoc iated with muscle paralysis and atrophy.
13例行运动神经元生存基因 (SMN)检测 ,11例外显子 7和 8联合缺失 ,1例仅第 7外显子缺失 ,1例仅第 8外显子缺失。收藏指正
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