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991.
上海市不同人群人芽囊原虫感染调查 总被引:3,自引:0,他引:3
目的了解上海市不同人群人芽囊原虫感染情况。方法在上海市6个区收集居民新鲜粪便,采用Ringer溶液37℃恒温条件下培养人芽囊原虫,计算人芽囊原虫感染率。结果检查居民2 984人,人芽囊原虫阳性者88人,感染率2.95%。上海市各区人群感染率间差异无统计学意义(χ~2=9.90,P>0.05);青浦区男性感染率为5.56%,女性感染率1.57%,差异有统计学意义(χ~2=5.38,P<0.05),其他5个区男、女性感染率差异无统计学意义(χ~2=0.08~0.54,P均>0.05);农民感染率为6.87%,与其他职业人群比较差异有统计学意义(χ~2=18.57,P<0.05)。结论上海市人群对人芽囊原虫普遍易感,以农民感染率最高。体外培养法敏感性较高.可用于人芽囊原虫感染的流行病学调查。 相似文献
992.
The nadir of SaO2 during an obstructive apnea is dependent upon the apnea's duration and the rate of fall of saturation (dSaO2/dt). We postulated that a low Q, such as in patients with congestive heart failure with sleep apnea, or a reduction in Q, as seen in some humans during obstructive sleep apnea, might steepen dSaO2/dt. The mechanism postulated was lowering of SvO2 with increased pulmonary capillary blood oxygen uptake and faster depletion of alveolar oxygen. This study examines dSaO2/dt following the onset of apnea in eight spontaneously breathing adult baboons. Nonrepetitive obstructive apneas (30, 45, and 60 seconds) were created by clamping an indwelling cuffed endotracheal tube at the end of expiration. Following baseline measurements, the animals were given a bolus of a rapid-acting beta-adrenergic blocker followed by continuous infusion to reduce cardiac output and to limit the cardiovascular response to obstructive asphyxia. Fiberoptic catheters were used for continuous monitoring of SaO2, SvO2, and cardiac output. Esophageal pressure and relative thoracic gas volume (Respitrace) were monitored to insure equivalence of lung volume at the onset of apnea. Beta-adrenergic blockade reduced resting Q by a mean of 25 percent. The blocked vs unblocked dSaO2/dt was 0.73 vs 0.72 percent/s, 0.76 vs 0.73 percent/s, and 0.70 vs 0.71 percent/s for 30-second, 45-second, and 60-second apneas, respectively. Thus, mean dSaO2/dt for all durations of apneas was unaffected by beta-adrenergic blockade. We concluded that dSaO2/dt is not influenced by limited Q preceding or induced by obstructive asphyxia. 相似文献
993.
Ying-Bin Liu Shun-Liang Gao Xiao-Peng Chen Shu-You Peng He-Qing Fang Yu-Lian Wu Cheng-Hong Peng Zhe Tang Bin Xu Jian-Wei Wang Gui-Long Deng Hai-Jun Li Xue-Dong Feng Hao-Ran Qian Department of Surgery Second Affiliated Hospital of Medical School of Zhejiang University Hangzhou Zhejiang Province China 《World journal of gastroenterology : WJG》2005,(9)
994.
995.
抗日本血吸虫单克隆抗体的制备及其在诊断中的应用 总被引:4,自引:1,他引:4
The present paper reported on an anti-CCA monoclonal antibody, McAb-IIID 10, which could be used in determinations of both parasite-oriented circulating antigens and specific anti-CCA antibodies. The established competitive ELISA (C-ELISA) using McAb-IIID 10 to detect schistosome-antibodies showed high sensitivity and specificity in the diagnosis of schistosomiasis with few cross-reactions. In field trials, coincident rates in 3 separate batches of serum samples when subjected to double-blind detections were obtained. A total of 1,915 serum samples had been determined by C-ELISA, among them 113 acute cases achieved a 100% positive rate, 765 chronic and 25 late cases showed 96.3% and 72% positive respectively. 70% of the 66 cured schistosomiasis cases turned to be negative. None of the 750 normal individuals showed positive reactions. No cross reaction was found in 27 sera from hydatidosis, whereas 1 and 2 positive reactions were found in 43 paragonimiasis sera and 126 clonorchiasis sera respectively. The established McAb-IIID 10 involved Dot-ELISA was found of value in the assessment of effective chemotherapy and showed a high negative conversion rate of 97.9% in 48 cured schistosomiasis patients. In 16 experimentally infected rabbits, 12 became negative in Dot-ELISA determinations at the 8th week post treatment, and the remaining 4 treated ones, the titer as well as the reaction intensity were also found reduced. A good coincidence rate was also found between C-ELISA and Dot-ELISA, their detection results may be complementary each other. 相似文献
996.
Function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus 总被引:4,自引:0,他引:4
Chen Z Mi L Xu J Yu J Wang X Jiang J Xing J Shang P Qian A Li Y Shaw PX Wang J Duan S Ding J Fan C Zhang Y Yang Y Yu X Feng Q Li B Yao X Zhang Z Li L Xue X Zhu P 《The Journal of infectious diseases》2005,191(5):755-760
To identify the function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome (SARS) coronavirus (CoV), we analyzed the protein-protein interaction among HAb18G/CD147, cyclophilin A (CyPA), and SARS-CoV structural proteins by coimmunoprecipitation and surface plasmon resonance analysis. Although none of the SARS-CoV proteins was found to be directly bound to HAb18G/CD147, the nucleocapsid (N) protein of SARS-CoV was bound to CyPA, which interacted with HAb18G/CD147. Further research showed that HAb18G/CD147, a transmembrane molecule, was highly expressed on 293 cells and that CyPA was integrated with SARS-CoV. HAb18G/CD147-antagonistic peptide (AP)-9, an AP of HAb18G/CD147, had a high rate of binding to 293 cells and an inhibitory effect on SARS-CoV. These results show that HAb18G/CD147, mediated by CyPA bound to SARS-CoV N protein, plays a functional role in facilitating invasion of host cells by SARS-CoV. Our findings provide some evidence for the cytologic mechanism of invasion by SARS-CoV and provide a molecular basis for screening anti-SARS drugs. 相似文献
997.
目的 观察丹参通脉胶囊对脑缺血再灌注大鼠的影响,探究其脑组织恢复程度。方法 取SD大鼠40只,制备脑缺血再灌注损伤模型(MCAO),实验大鼠随机分为假手术组、模型组、血塞通组及丹参通脉胶囊组,观察脑缺血再灌注24 h后大鼠神经行为学评分、脑组织含水量、脑梗死体积、局部脑皮层血流量(rCBF)和局部微血管内皮细胞的变化情况。结果 与模型组及血塞通组比较,丹参通脉胶囊能显著降低大鼠的神经行为学评分(P<0.01);降低脑组织含水量(P<0.01);减小脑梗死体积(P<0.01);提高局部脑组织血流量(P<0.01);增加微血管内皮细胞的数量(P<0.01)。结论 丹参通脉胶囊对大鼠脑缺血再灌注损伤具有保护作用,可加速脑组织恢复。 相似文献
998.
999.
Tao Zhang Hua Cheng Zhenyu Pan Jie Mi Yuzhu Dong Ying Zhang Dan Sun Qian Du Xiaoliang Cheng Yalin Dong 《Basic & clinical pharmacology & toxicology》2020,126(1):75-85
A vancomycin steady‐state trough concentration (Cmin) of 15‐20 mg/L is recommended for achieving a ratio of the 24‐hour area under the curve to the minimum inhibitory concentration (AUC0‐24/MIC) of ≥400 in adults. Since few paediatric data are available, our objectives were to (a) measure the pharmacokinetic indices of vancomycin and (b) determine the correlation between Cmin and AUC0‐24/MIC in paediatric patients. Population‐based pharmacokinetic modelling was performed for paediatric patients to estimate the individual parameters. The relationship between Cmin and the calculated AUC0‐24/MIC was explored using linear regression and a probabilistic framework. A sensitivity analysis was also conducted using Monte Carlo simulations. Body‐weight significantly influenced the pharmacokinetics of vancomycin. Based on real data and simulations, Cmin ranges of 5.0‐5.9 and 9.0‐12.9 mg/L were associated with AUC0‐24/MIC ≥400 for MIC values of ≤0.5 and ≤1 mg/L, respectively. Vancomycin regimens of 10 and 15 mg/kg every 6 hours achieved a Cmin of 5.0‐5.9 mg/L and AUC0‐24/MIC ≥400 in >90% of the children when MIC was ≤0.5 mg/L. At a MIC of ≤1 mg/L, vancomycin at 15 mg/kg every 6 hours achieved Cmin of 9.0‐12.9 mg/L and AUC0‐24/MIC ≥400 in 2.0‐ and 1.6‐fold as many children compared to a dose of 10 mg/kg every 6 hours, respectively. Vancomycin Cmin values of 5.0‐12.9 mg/L were strongly predictive of achieving AUC0‐24/MIC ≥400, and rational dosing regimens of 10‐15 mg/kg q6h were required in paediatric patients, depending on the pathogen. 相似文献
1000.
Xiaohan Zhou Kun Shi Ying Hao Chengli Yang Ruoyu Zha Cheng Yi Zhiyong Qian 《Asian Journal of Pharmaceutical Sciences》2020,15(1):26-41
Oral tyrosine kinase inhibitors(TKIs) against epidermal growth factor receptor(EGFR) family have been introduced into the clinic to treat human malignancies for decades. Despite superior properties of EGFR-TKIs as small molecule targeted drugs, their applications are still restricted due to their low solubility, capricious oral bioavailability, large requirement of daily dose, high binding tendency to plasma albumin and initial/acquired drug resistance. Nanotechnology is a promising tool to improve efficacy of these drugs. Through non-oral routes. Various nanotechnology-based delivery approaches have been developed for providing efficient delivery of EGFR-TKIs with a better pharmacokinetic profile and tissue-targeting ability. This review aims to indicate the advantage of nanocarriers for EGFR-TKIs delivery. 相似文献