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   neurogenic 在 神经病学 分类中 的翻译结果: 查询用时:0.01秒
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neurogenic
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  神经源性
    Clinical Analysis of 42 Cases with Neurogenic Claudication
    神经源性间歇跛行42例临床分析
短句来源
    Radiological and CT Analysis of Neurogenic Tumors of the Sacrum: Report of 6 Cases
    骶骨神经源性肿瘤的X线平片及CT分析(附6例报告)
短句来源
    Imaging diagnosis of neurogenic tumors of the brachial plexus
    臂丛区神经源性肿瘤的影像学诊断
短句来源
    MRI Diagnosis of Sacral Neurogenic Tumors
    骶椎神经源性肿瘤MRI诊断
短句来源
    Clinical Analysis of 10 Cases of Neurogenic Pulmonary Edema Complicated by Cerebral Hemorrhage
    脑出血神经源性肺水肿10例临床分析
短句来源
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  神经原性
    Quantitative Histopathologic Study of Biopsied Muscle Specimens in Patients with Neurogenic Amyotrophy
    神经原性肌萎缩的肌肉组织病理定量研究
短句来源
    Results: In the 78 motor nerves examined,reduction of MCV was found in 44.8% of upper and lower limbs,prolongation of the distal latency in 24.3%,reduction of SCV in 38.1%,F waves abnormality in 89.3%,and the neurogenic changes revealed by EMG were found in 64.5%.
    结果:上、下肢MCV减慢占44.8%. 远端潜伏期延长占24.3%,SCV减慢占38.1%,F波异常占89.3%,EMG提示神经原性改变占64.5%。
短句来源
    Results:EMG was abnormal and shows neurogenic damage in all the involved 188 muscles.
    结果:损伤神经支配的188块肌肉EMG结果均为神经原性损伤。
短句来源
    HL-329 Blocks Neurogenic Plasma Extravasation in Rat Dura Mater
    HL-329抑制大鼠硬脑膜内神经原性血浆蛋白渗出
短句来源
    Secretoneurin and neurogenic inflammation
    Secretoneurin和神经原性炎症(英文)
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  “neurogenic”译为未确定词的双语例句
    Results:As a single parameter,the area produced a better result in discriminating neurogenic MUP from control,with 73 2%-79 6% of MUP from neurogenic muscles being judged as abnormal and 14 7%-15 7% MUP from normal muscles being misclassified.
    结果 :单一参数中 ,面积的诊断作用最敏感 ,可判别 73 2 %~ 79 6%的神经病变组MUP。
短句来源
    Methods Retrospective analyzed the diagnosis and outcome of 10 cases of neurogenic pulmonary edema complicated by cerebral hemorrhage.
    方法 对 10例脑出血后并发神经源性肺水肿病例进行回顾性总结与分析 ,诊断以及病性转归初步分析与总结。
短句来源
    EMG showed neurogenic disorder. The result of treatment was as follows: cure in 5(41.7%), markedly effective in 2(16.7%), improved in 2(16.7%), and unchanged in 3 (25.0%). The general effective rate was 75%.
    高压氧联合药物治疗结果治愈 5例 ( 4 1.7% ) ,显效 2例 ( 16.7% ) ,好转 2例 ( 16.7% ) ,无效 3例 ( 2 5 .0 % ) ,总有效率 75 %。
短句来源
    In the CMT group, we could find the amyotrophy of legs in 106 patients (96.4%), distal muscle weakness and atrophy of the upper limbs in 48 patients (43.6%), stork legs in 64 patients (58.2%), pes cavus in 68 patients (61.8%), decreased or diminished tendom reflexes in 108 patients (98.2%). Electromyography examination in 61 patients showed neurogenic damages.
    表现双下肢肌萎缩106例( 96. 4% ),双上肢远端肌无力与肌萎缩48例( 43. 6% ),鹤立腿64例(58 .2% ),弓形足68例(61. 8% ),踝反射减弱及消失108例(98 .2% )。
短句来源
    Muscle biopsy and nerve biopsy exhibited neurogenic lesion and chronic moderate axonal neuropathy respectively in 1 case.
    1例神经活检示慢性中度轴索性神经病。
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  neurogenic
On the Role of β-Adrenoreceptors in Mechanisms Underlying Neurogenic Dystrophies
      
Propranolol exerted an antidystrophic effect in the case of local damages of the nervous system and, thereby, prevented the development of neurogenic dystrophies.
      
Mechanisms of neurogenic dystrophies induced by activation and deprivation of the sympathetic nervous system
      
β-Blocker propranolol was shown to exert an antidystrophic effect in the case of local injuries of the neural system and, thus, prevented the development of neurogenic dystrophies.
      
The results are discussed in the context of disruption of the immune system neurohumoral regulation and development of neurogenic immunity deficiency and its different types.
      
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31 cases of neurogenic mediastinai tumours were reported. All Except one were located in the posterier mediastinum. Retrospective study of the 30 cases revealed that most of the ganglioneuromas could be distinguished radiographically from the tumours of neural sheath origin. 3 cases were misdiagnosed as lung lesions. Further examination for the demonstration of extrapleural sign was emphasized in differential diagnosis.

本文分析了31例纵隔神经源肿瘤的临床、X线资料。肿瘤除1例在前纵隔外,其余30例均位于后纵隔。回顾分析这30例,有25例根据X线表现可判断为节细胞神经瘤与神经鞘源性肿瘤(包括神经纤维瘤与神经鞘瘤)。3例误诊为肺内病变,提高胸膜外征的显示率对它们之间的鉴别诊断是有帮助的。

The histogenetic origin of the meduilobiastoma is still controversial. Ten cases of meduiloblastoma, one case of fetal cerebellum and one case of adult cerebellum were collected in this paper, the specimens were observed with light and electron microscope.The meduiloblastoma are chiefiy composed of undifferentiated blast cells, some of which showed neurogenic differentiation character. Under the light microscope rosetter may be seen, and under the electron microscope axon-like structure, synaptic-like...

The histogenetic origin of the meduilobiastoma is still controversial. Ten cases of meduiloblastoma, one case of fetal cerebellum and one case of adult cerebellum were collected in this paper, the specimens were observed with light and electron microscope.The meduiloblastoma are chiefiy composed of undifferentiated blast cells, some of which showed neurogenic differentiation character. Under the light microscope rosetter may be seen, and under the electron microscope axon-like structure, synaptic-like structure and dense core granules have been identified. Some tumor cells showed glialcell character with processes positively stained by phosphotungstic acid hematoxylin. Under the electron microscope there were bundles of glial fibrils evident in the cell bodies and processes. The above observation suggests that the tumor cells have a capacity for maturation toward nerve cells and glial cells. The tumor cells had similar morphologic character to the cells of zona granulosa exierna of fetal cerebellum but not to that of adult cells of zona granulosa interna, so we suggest that these tumors may be originated from zona granulosa nexteraa cerebella or its vestiges, but not from granulosa neurons.

关于髓母细胞瘤的组织学起源问题,至今仍有争论。本文收集髓母细胞瘤10例、8个半月胎儿小脑1例和成人小脑1例,分别进行光镜和电镜观察。髓母细胞瘤细胞主要是未分化的原始细胞。有的瘤细胞表现神经元性分化特点,光镜下出现菊形团排列,电镜下出现轴突样结构、突触样结构和致密核心小泡。有的瘤细胞则表现星形细胞特点,分化出磷钨酸苏木素染色阳性突起的幼稚的成胶质细胞和星形细胞,电镜下细胞的胞体和突起内出现成束的胶质微丝。表明了髓母细胞瘤是一种神经上皮性肿瘤,瘤细胞具有双向分化的潜能。髓母细胞瘤细胞和胎儿小脑外颗粒层细胞在形态上有很大相似性,和成人内颗粒层细胞在形态上没有相似性,说明在神经上皮之中,本瘤更可能起源于小脑外颗粒层或其残余,而不是起源于颗粒神经元。

The histogenetic origin and cellular differentiation of medulloblastoma are still controversial. Ten cases of medulloblastoma, one case of fetal cerebellum and one case of adult cerebellum were observed with light and electron microscopy.The medulloblastoma were chiefly composed of iundifferentiated primitive cells. Some tumor cells showed neurogenic differentiation. Under the light microscope rosetters were seen, and under the electron microscope axon-like structure, synaptic-like structure and dense...

The histogenetic origin and cellular differentiation of medulloblastoma are still controversial. Ten cases of medulloblastoma, one case of fetal cerebellum and one case of adult cerebellum were observed with light and electron microscopy.The medulloblastoma were chiefly composed of iundifferentiated primitive cells. Some tumor cells showed neurogenic differentiation. Under the light microscope rosetters were seen, and under the electron microscope axon-like structure, synaptic-like structure and dense core granules were identified. Some tumor cells showed glial cell character with processes positively stained by phosphotungstic acid hematoxylin. Unedr the electron microscope there were bundles of glial fibrils in the cell bodies and processes. According to the above observations, we suggest that the tumor is a neuroepithelial tumor an 1 tumor cells have a capacity to differentiate nervous cells and glial cells. The tumor cells were similar to the cells of the external granular layer of fetal cerebllum. We suggest that medulloblastoma may be originated from the external granular layer of cerebellum or its vestiges.

髓母细胞瘤的组织学起源和细胞分化至今仍有争论。本文收集髓母细胞瘤10例、81/2月胎儿小脑1例和成人小脑1例,进行光镜和电镜观察。髓母细胞瘤细胞主要是未分化的原始细胞。有的瘤细胞表 现神经元性分化,光镜下出现菊形团,电镜下出现轴突样结构、突触样结构和致密核心小泡。有的瘤细胞表现星形细胞特点,分化出磷钨酸苏木素染色阳性的幼稚成胶质细胞和星形细胞,电镜下细胞胞体和突起内有成束的微丝。表明髓母细胞瘤是一种神经上皮性肿瘤,瘤细胞具有双向分化的潜能。髓母细胞瘤细胞和胎儿小脑外颗粒层细胞有很大相似性。在神经上皮之中,本瘤更可能起源于小脑外颗粒层或其残余。

 
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