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1.
刘素艳 《中华综合医学杂志(哈尔滨)》2005,6(3):204-205
目的:探讨尿激酶与急性脑梗死(ACI)患者特异性烯醇化酶(NSE)的关系。方法:该实验采用酶联免疫吸附法(EusA)测定脑梗死常规治疗组、尿激酶治疗组血清NSE水平。结果:尿激酶组NSE值显著低于ACI常规治疗组。结论:尿激酶能降低血清酶活性,使已形成的纤维蛋白水解,从而缩小梗死灶体积,改善脑缺血、缺氧,从而起到保护脑细胞的作用。 相似文献
2.
目的 探讨新生儿缺氧缺血性脑病时神经元烯醇化酶的变化,为HIE的诊断和治疗提供依据。方法 采用病历对照研究,将实验组分为三组:轻、中、重度HIE分别为2 1、4 9、8例;正常对照组73例。测定其血中神经元烯醇化酶的浓度变化。比较各组间检测指标的差异。结果 实验组NSE水平明显高于对照组,组间有显著性差异,P <0 .0 1:且实验组轻、中、重度间有显著性差异,P均<0 .0 5。结论 NSE水平与HIE的病情严重程度相关,是反映HIE严重程度比较客观的指标。 相似文献
3.
高压氧对大鼠局灶性脑缺血再灌注时神经元特异性烯醇化酶的影响 总被引:2,自引:1,他引:1
目的研究高压氧(HBO)对大鼠局灶性脑缺血再灌注(IR)时.大鼠脑梗塞体积.脑组织病理改变及神经元特异性烯醇化酶(NSE)含量的影响。方法用线栓法制备阻断大脑中动脉(MCA)的局灶性脑IR模型。Wistar大鼠30只,随机分为5组:正常对照组(N组n=-6),缺血再灌注2h 常压空气组(Rt组,n=-6),缺血再灌注24h 常压空气组(R2组,n=-6),缺血再灌注2h HBO组(H1组,n=-6),缺血再灌注24h HBO组(H2组,n=-6)。R1、R2、H1、H2组缺血时间均为2h。R1、R2组暴露于常压空气,H1、H2组暴露于2.5MPa氧气。病理切片用HE染色,用Swanson方法测定脑梗塞体积,用酶联免疫法测定NSE含量。结果H1、H2组与R1、R2组相比,神经元缺血性损害较轻,脑梗塞体积缩小,NSE含量明显下降,差异有统计学意义。结论HBO能减轻缺血性脑损害,保护脑组织。 相似文献
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目的通过测定戊四氮致痫大鼠脑脊液中的神经元特异性烯醇化酶(NSE)水平的变化,探讨痫性发作与脑损伤之间的关系。方法110只Wistar大鼠分为实验组和对照组。实验组给予戊四氮(PIZ)腹腔注射。根据痫性发作的强度分为轻度组和重度组。用酶联免疫吸附法(ELISA)测定不同痫性发作强度、不同时间点大鼠脑脊液中NSE水平的变化,并与对照组进行对比。结果重度组脑脊液NSE水平在1h、2h、4h、6h均显著高于轻度组和对照组(P<0.01);轻度组脑脊液NSE含量在1h高于对照组(P<0.05),在2h、4h、6h显著高于轻度组;脑脊液NSE水平在痫性发作后1h迅速升高。4h达到高峰,24h恢复到正常水平。结论痫性发作可对大鼠神经细胞造成明显的损害。损害的程度与痫性发作的程度有关。痫性发作后4h可能是进行早期干预、防止脑细胞损伤的时间窗。 相似文献
7.
Judith Nemeth Annie Galian Jacqueline Mikol Béatrix Cochand-Priollet Michel Wassef Anne Lavergne 《Virchows Archiv : an international journal of pathology》1987,412(1):89-93
Summary The immunoreactivity of polyclonal antiserum to neuron-specific enolase (NSE) has been investigated. Twenty-three cases of malignant lymphoma (ML) were studied and compared with previously published reports. In our study 11 out of 23 cases showed strong or weak NSE positivity; any type of ML could be positive or negative even among B or T cell ML. This study indicated that polyclonal NSE is not a specific marker; it might be an inconstant marker of ML with no apparent correlation between reactivity and morphology or phenotype. 相似文献
8.
Summary A large series of central and peripheral nervous system tumors was studied for the presence of glial fibrillary acidic protein (GFAP) and -enolase (neuron-specific enolase, NSE), using specific monoclonal antibodies (mAbs). Occurrence in and specificity of GFAP to glial and mixed tumors was confirmed and depended on the malignancy grade and features such as meningeal invasion. Using a well-characterized mAb, -enolase was demonstrated in neuronal, as well as in a whole range of non-neuronal tumors. This lack of specificity of -enolase prohibits its use as an exclusive neuronal marker. Nevertheless quantization or comparison with other types of enolases could still prove to be useful in well-defined situations. The advantages inherent to mAbs and a highly sensitive detection system turn GFAP stainings into a specific and readily reproducible technique.Supported in part by FGWO (grant no. 3.0019.86) and by the Geconcerteerde Actie (grant no. 84/89-68, Brain specific proteins) 相似文献
9.
Tomoko Kamishima Takeaki Fukuda Toshio Kakihara Yoshihisa Ohnishi Makoto Naito Hidenori Ueki Shinzo Tachikawa 《Pathology international》1993,43(10):615-623
A case of small round and spindle cell sarcoma with neuronal differentiation and oncocyte-like features is presented. The tumor was encountered in a 32 year old Japanese woman with an initial presentation of palpable tumor in the left lateral region of the thorax. The resected tumor was a partially well encapsulated whitish medullary one and consisted of small round and spindle tumor cells, together with so-called rhabdoid cells in the small round cell area. Although pseudorosettes were often observed, true rosette formation could not be detected anywhere. Ultrastructurally, despite a histologic variety of tumor cells, most tumor cells possessed numerous mitochondria, some of which occasionally contained abnormal filamentous or crystalloid structures. Various amounts of microfilaments were present in most tumor cells and microtubules were present in a few. A minority of small round cells possessed a small number of neurosecretory granules, especially in short cytoplasmic processes. A positive immunoreaction for neuron specific enolase was found by immunohistochemical examination in several small round tumor cells and for neurofilaments in lesser numbers. Despite the lack of S-100 protein, MB2 was detected in both small round and spindle cells. On the basis of these findings, the tumor of the present case corresponds to malignant peripheral nerve sheath tumor with neuronal differentiation and oncocytic features. 相似文献
10.
J Peltzer L Colman J Cebrian H Musa M Peckham A Keller 《Developmental dynamics》2008,237(5):1412-1423
We have investigated whether the phenotype of myogenic clones derived from satellite cells of different muscles from the transgenic immortomouse depended on muscle type origin. Clones derived from neonatal, or 6- to 12-week-old fast and slow muscles, were analyzed for myosin and enolase isoforms as phenotypic markers. All clones derived from slow-oxidative muscles differentiated into myotubes with a preferentially slow contractile phenotype, whereas some clones derived from rapid-glycolytic or neonatal muscles expressed both fast and slow myosin isoforms. Thus, muscle origin appears to bias myosin isoform expression in myotubes. The neonatal clone (WTt) was cultivated in various medium and substrate conditions, allowing us to determine optimized conditions for their differentiation. Matrigel allowed expressions of adult myosin isoforms, and an isozymic switch from embryonic alpha- toward muscle-specific beta-enolase, never previously observed in vitro. These cells will be a useful model for in vitro studies of muscle fiber maturation and plasticity. 相似文献