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临床     
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  clinical
    Clinical and Molecular Genetic Study of Dopa-responsive Dystonia
    多巴敏感性肌张力障碍临床和分子遗传学研究
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    The Clinical and Neuropathological Study in Patients with Cerebral Amyloid Angiopathy
    淀粉样脑血管病的临床和神经病理学研究
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    Studies on Clinical and Biological Behaviors and Anatomic Comparative Surgical Approaches of Median Skull Base Tumor
    中间颅底肿瘤临床生物学行为及手术入路解剖比较研究
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    The Experimental and Clinical Study on Neuron Functional Imaging for Parkinson's Disease
    帕金森病的实验和临床神经功能影像学研究
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    Experimental and Clinical Application of MR Functional Techniques in the Study of Cerebral Gliomas
    脑胶质瘤磁共振功能成像的实验与临床应用研究
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  clinic
    Study on the Clinic, Pathology, Epidemiology of HSLE and the Cytochrome P4502D6 Genetic Polymorphism with the Susceptibility of HSLE
    海洛因海绵状白质脑病的临床、病理、流行病学调查和CYP4502D6基因多态性关系的研究
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    CLINIC ANALYSIS OF 30 CASES WITH MULTI-INFARCT DEMENTIA
    30例多梗塞性痴呆的临床分析
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    54 Cases of Thalamic Hemorrhage——Clinic and CT
    丘脑出血54例—临床与CT
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    CT and Clinic of Brain abscess
    24例脑脓肿的CT与临床
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    SENILE SUBCORTICAL ARTER IOSCLEROTIC ENCEPHALOPATHY CT AND CLINIC
    老年皮质下动脉硬化性脑病——CT与临床
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  clinical manifestations
    CLINICAL MANIFESTATIONS OF ACOUSTIC NEUROMA
    听神经瘤临床表现分析
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    Clinical Manifestations of Partial Seizures with Complicated Symptoms——Analysis of 100 Cases
    伴复杂症状的部分性癫痫的临床表现——附100例临床资料分析
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    A Comparison of the Results of Brain SPECT and the Clinical Manifestations for Cerebral Ischemic Vascular Diseases
    缺血性脑血管病的脑SPECT结果与临床分析
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    Vertebrobasilar Insuffioienoy in the Aged:A Study of Clinical Manifestations and BAEP
    老年人椎基动脉供血不足的临床表现与BAEP研究
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    A Analysis on the Relations Between the Clinical Manifestations and EKG in 90 Cases of Subarachnoid Hemorrhage
    90例蛛网膜下腔出血临床与心电图关系分析
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  clinical expressions
    Methods The character of clinical expressions and signs in the 5 patients with their results of laboratory and pathology were reported.
    方法 报告各患者的临床表现体征之特点、实验室检查及病理结果 ,结合近 5年国外文献进行发病机制及治疗方面的讨论。
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    Methods Among the 312 cerebral infarction patients 36 HI patients were founded. The 36 HI patients had been studied in picture changes, clinical expressions and the results of diagnosis and treatment.
    方法总结分析临床312例脑梗死患者中36例出血性梗死的影像学改变,临床表现和诊治结果.
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    Methods The characteristics of clinical expressions and signs were reported, muscle biopsy was did and pathologic findings and pathogenesis were discussed.
    方法 报告 1例成人晚发型杆状体肌病患者的临床表现、实验室及肌肉病理检查 ,结合国内外文献进行病理改变及发病机制方面的讨论。
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      clinical
    Guanidine-type compounds that reached clinical status include amongst others the potassium channel opener, pinacidil and the histamine H2-receptor antagonists (e.g.
          
    (ii) Other compounds have proceeded through preclinical and/or clinical development: CXCR4 antagonists (i.e.
          
    (iii) Yet other compounds, acting by novel mechanisms, have recently been identified as anti-HIV agents that seem worthy of further (pre)clinical development: cell receptor CD4 downmodulators (i.e.
          
    PRE-CLINICAL AND CLINICAL PHARMACOKINETICS OF THE DIASTEREOMERS OF ARTEETHER, A POTENT ANTIMALARIAL
          
    Pre-clinical studies were carried out (N=3) by oral, intramuscular and intravenous routes, while clinical studies (N=13) were performed intramuscularly.
          
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      clinic
    The applicability and efficiency of the electroencephalogram (EEG)-based method of biofeedback (BFB) training in correcting functional disorders in pregnancy have been evaluated in an obstetric/gynecological clinic in 65 pregnant women.
          
    An epithermal neutron source based on a compact tandem accelerator is being built at the Budker Institute of Nuclear Physics for use in neutron capture therapy at a cancer clinic.
          
    The data obtained shed light on some specific features in the composition of clayey rocks, which can be used for mud cure of arthritis and rheumatism in the Health and Rehabilitation Clinic of the Nature Health Association of Iceland, Hveragerei.
          
    Mono- clinic system, space group C2/c, a = 13.4877(10), b = 9.5843(7), c = 7.9564(6) ?, β = 116.124(2)°, V = 923.45(12) ?3.
          
    The crystals are mono-clinic: a= 14.678(3) ?, b= 11.866(2) ?, c= 19.655(4) ?, β = 102.17(3)°, V= 3346(1) ?3, Z= 4, ρcalcd= 1.364 g/cm3, space group C2/c.
          
    更多          
      clinical manifestations
    Clinical manifestations and outcomes in severe ulcerative colitis
          
    In order to evaluate the clinical manifestations and outcomes of severe ulcerative colitis (UC), we retrospectively reviewed 41 patients with severe UC from 144 consecutively hospitalized UC cases from 1988 to 2004.
          
    The ARVC, usually presenting with different clinical manifestations and pathological changes, were mainly seen in young men and is one of the main causes of sudden death in the young.
          
    Intrahemispheric coherence of the EEG depending on clinical manifestations of temporal epilepsy in children
          
    Significant interhemispheric differences in coherence dependent on clinical manifestations of the disease were detected.
          
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      clinical expressions
    Adynamia episodica and paramyotonia congenita are occasionally regarded as different clinical expressions of a common underlying disease.
          
    McArdle's disease: two clinical expressions in the same pedigree
          
    Clinical expressions of cognition and behaviour in Alzheimer's disease (AD) patients are heterogeneous.
          
    Conversely, different clinical expressions of the defect of a single enzyme may be attributed to allelic mutations.
          
    Familial CDI is a hereditary form of primary CDI with a variety of clinical expressions among affected individuals which is said to be related to varying degrees of an arginine vasopressin (AVP) deficiency.
          
    更多          


    This is a clinico-electroencephalographic report of seven typical cases of subacute sclerosing panencephalitis with a discussion of certain aspects of the disease. Correct and early diagnosis of the disease hinges on the total clinical picture rather than any isolated symptom or/and sign. The diagnosis of this disease is more aptly established if the case is associated with fairly typical EEG findings, biochemical and immunological studies of the blood and spinal fluid and morphological findings of the biopsied...

    This is a clinico-electroencephalographic report of seven typical cases of subacute sclerosing panencephalitis with a discussion of certain aspects of the disease. Correct and early diagnosis of the disease hinges on the total clinical picture rather than any isolated symptom or/and sign. The diagnosis of this disease is more aptly established if the case is associated with fairly typical EEG findings, biochemical and immunological studies of the blood and spinal fluid and morphological findings of the biopsied specimen of the brain. Case 2 was a boy of 7 years old who had been noted to have speech difficulty and memory defect for several months and one generalized seizure the day before he was seen on Feb. 8, 1977. Under the treatment of anticonvulsants and steroids he apparently had two periods of remission. He contracted measles two years after the onset of his illness but without evident symptoms. Case 6 had been treated in a mental hospital as a case of schizophrenia. The corrent diagnosis in this case was made on the basis of the total clinical picture and EEG findings. Anticonvulsants , cytoarabinose , amantadine , steriod , supportive measures and good nursing care have made him more alert and improved his general condition to the satisfaction of his family though he is still demented. Both these two cases had had serial EEG examinations.

    本文报告了临床和脑电图?见

    155 cases of sporadic encephalitis are reported. Among these cases,13 were autopsied. This is a disorder characterized by diverse impairmentsof the central nervous system such as psychiatric disturbance, unconsci-ousness, epilepsy, paralysis, decortical state, etc. In the majority ofthe subjects studies, infectious features were not prominent and therewere no changes in the cerebral spinal fluid. However, in a few cases,slight pleocytosis with a mild increase of protein in the CSF or slightincrease of the intracranial...

    155 cases of sporadic encephalitis are reported. Among these cases,13 were autopsied. This is a disorder characterized by diverse impairmentsof the central nervous system such as psychiatric disturbance, unconsci-ousness, epilepsy, paralysis, decortical state, etc. In the majority ofthe subjects studies, infectious features were not prominent and therewere no changes in the cerebral spinal fluid. However, in a few cases,slight pleocytosis with a mild increase of protein in the CSF or slightincrease of the intracranial pressure was recorded. On the basis of the clinical manifestation, these cases were dividedinto five groups: (1) psychiatric type, (2) intracranial hypertension type,(3) epileptic type, (4) protean clinical manifestation type, and (5) para-lytic type. On pathological examination, two forms were observed. Onewas compatible with virus encephalitis, while another with demyelinateencephalitis. However, pathologically these two forms could be clearlydistinguished, but clinically they were not. It is assumed that sporadic encephalitis may be resulted from morethan one cause. The diagnosis and elucidation of the nature of thedisease need further investigation.

    本文报告散发性脑炎155例,其中13例进行尸解,发现有两类病理改变,一种符合病毒性脑炎;另一种符合急性脱髓鞘性脑炎。两种病例在临床上不易鉴别。因此,对本病的诊断有待从病原学,免疫学及电镜检查等方面进行探索。

    Sturge-Weber syndrome is a congenital disorder with a familial tendency and an irregular dominant heredity. Clinically it is characterized by the presence of cutaneous vascular nevi, convulsive seizures, mental disturbances, buphthalmus, spastic hemiplegia and one-sided hypotrophy of extremites. Roentgenologically intracranial patches or double-contour wavy shadows or multiple flecks are seen in the skull. Pneumoencephalograms reveal atrophy of cerebral hemisphere and dilatation of lateral ventricles of the...

    Sturge-Weber syndrome is a congenital disorder with a familial tendency and an irregular dominant heredity. Clinically it is characterized by the presence of cutaneous vascular nevi, convulsive seizures, mental disturbances, buphthalmus, spastic hemiplegia and one-sided hypotrophy of extremites. Roentgenologically intracranial patches or double-contour wavy shadows or multiple flecks are seen in the skull. Pneumoencephalograms reveal atrophy of cerebral hemisphere and dilatation of lateral ventricles of the corresponding side. Electroencephalographic studies show reduction in amplitude, sharp wave or slow wave focus on the same side as the cutaneous vascular nevi. Pathologically angiomatous changes of face and meninges, calcification in cortical layer and cerebral capillary wall, diminution of ganglion cells and gliosis are evident. The present article is a clinical analysis of 22 cases seen in 1936~1978, Three illustrative cases are appended.

    Sturge-Weber二氏综合征是先天性疾患,似属显性遗传。临床上以皮肤血管痣、搐搦发作、精神症状、眼球突出、痉挛性偏瘫及半身萎缩为特征。颅骨片于枕部示片状或双层波状钙化灶。气脑造影示相应侧大脑半球脑沟增宽及脑室扩大。病理方面皮肤及脑膜有血管痣,脑皮质有钙化灶,神经细胞减少及胶质细胞增生。脑电图常有一侧波幅降低或尖波慢波灶。神经精神症状系脑膜血管瘤压迫所致。本病散见于世界各种族。作者将1936~1978年所见之22例作了临床分析。并附3例病历摘要。

     
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