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myopathic相关的网络例句

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与 myopathic 相关的网络例句 [注:此内容来源于网络,仅供参考]

Clinical examination, intelligence tests, and develipmental examinations revealed myopathic facial weakness, passivity and delayed cognitive development.

临床理学,神经学检查,智力测验用发展测量评估显现病人有肌病变性面部肌肉无力,被动个性,及认知发展迟缓。

There is usually little or no progression, the EMG shows non-specific myopathic features and serum CK is normal or only slightly raised.1 The muscle biopsy may show characteristic ultrastructural abnormalities but these can be difficult to detect without specific histochemistry and/or electron microscopy that were not available in 1981 when our patient was biopsied.

经常表现为缓慢或者无明显进展,EMG提示非特异性肌源性改变特征,血清CK是正常的或者仅仅轻微的升高。肌肉活检可能表现为特征性的超微结构异常,但是这些改变必须通过特异性的组织化学和/或电镜才能观察。而在患者进行活检时的1981年这些手段是达不到的。

In normal myocardium, sorcin extensively co-localized with ryanodine receptors, whereas in myopathic hearts, the degree of co-localization was markedly disrupted.

正常心肌细胞中,sorcin与细胞内钙释放通道RyR能广泛协同定位,而在心肌病的心肌细胞中,这种协同定位的能力被破坏。

Motor unit potential ; Discriminant analysis ; Myopathic lesion ; Neurogenic lesion

运动单位电位;判别分析;肌源性损害;神经源性损害

The myopathic patterns of electromyography, especially the slowed mulscle fiber conduction velocity, might be as the diagnostic indicates of chronic alcoholic myopathy.

2肌电图提示肌源性改变,特别是肌纤维传导速度减慢,是诊断酒精中毒性肌肉病变的客观指征。

MethodsFrom the biceps brachii, tibialis anterior and vastus medialis muscles,the duration, amplitude, area and the ratio of area to amplitude of the MUPs were obtained by use of the spike-wave triggered average technique in 10 patients with myopathic disease, 13 patients with neurogenic disease and 22 healthy adults.

选取 10例肌肉病变患者、13例神经病变患者和 2 2例正常人,采用棘波触发平均技术,获取肱二头肌、胫前肌和股内侧肌MUP的时限、波幅、面积和面积/波幅比 4项参数,通过SPSS10 。0软件进行方差分析和判别分析。

The main abnormal findings were a shortening of the mean duration of MUAP and minority might show "myopathic changes" when needle EMG was conducted in MG patients.

MG患者常规EMG检查主要异常表现为MUAP时限缩短,少数可见&肌源性损害&的EMG表现。

Some are slowly progressive and a myopathic EMG may occur if there is an associated endplate myopathy (eg, in slow channel syndrome or acetylcholine esterase deficiency) or in DOK7 synaptopathy.

一部分缓慢进展,当伴随有终板的改变(如:在慢通道综合症或胆碱酯酶缺乏)或者在DOK7突触病时,EMG呈肌源性改变。

Among the abnormal 71 patients, 67 (94.4%) patients had a shortening of the mean duration of motor unit action potential. 37 (52.1%) an increase in polyphasia, 19 (26.8%) a full interference pattern of reduced amplitude during maximal voluntary effort and 3 (4.2%) abnormal fibrillations and positive sharps. 19 (26.8%) definite "myopathic changes".

在EMG异常者中,出现平均运动单位电位时限缩短67例(94.4%),多项波增多者37例(52.1%),大力收缩时募集电位呈病理干扰相19例(26.8%),异常自发电位3例(4.2%),结果符合&肌源性损害&表现19例(26.8%)。

There is usually little or no progression, the EMG shows non-specific myopathic features and serum CK is normal or only slightly raised.1 The muscle biopsy may show characteristic ultrastructural abnormalities but these can be difficult to detect without specific histochemistry and/or electron microscopy that were not available in 1981 when our patient was biopsied.

查体提示:双侧眼睑下垂,易疲劳;轻度面部及颈部肌肉无力;舌肌无力并出现中央沟。无眼肌麻痹。肩部上肢带肌消瘦、明显无力,可见肩胛翼。腰部无力,行走时脊柱前凸,呈&鸭步&步态。坐位是如不用双手辅助,可能掉出椅子外。但可以依靠其脚趾和足跟站立。患者肺活量为正常的80%,心电图及超声心动图正常。CK水平为正常的2-3倍。

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从鲍尔点的形成原理出发,分析对称连杆曲线上鲍尔点的产生条件,提出等边机构的对称连杆曲线上有单鲍尔点和双鲍尔点。

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