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1.
目的分析化学发光免疫法检验原发性肝癌肿瘤生物标志物[糖类抗原199(CA199)、甲胎蛋白(AFP)、癌胚抗原(CEA)、γ-谷氨酰转肽酶(γ-GT)]的应用价值。方法选择68例原发性肝癌患者作为观察组,另选取68例健康者作为对照组,所有研究人员均实施化学发光免疫法检验。观察比较两组肿瘤生物标志物CA199、AFP、CEA、γ-GT水平以及其阳性检出率,统计观察组肿瘤生物标志物联合阳性检出率。结果观察组患者肿瘤生物标志物CA19-9(53.52±10.37)U/ml、AFP(157.54±137.85)ng/ml、CEA(30.36±6.73)ng/ml、γ-GT(273.67±124.65)U/L均高于对照组的(4.63±0.68)U/ml、(1.67±0.25)ng/ml、(2.46±0.46)ng/ml、(32.58±11.78)U/L,差异均有统计学意义(P<0.05)。观察组患者的CA19-9、AFP、CEA、γ-GT阳性检出率分别为67.65%、47.06%、58.82%、80.88%,均高于对照组的0、0、0、0,差异均有统计学意义(P<0.05)。观察组患者肿瘤生物标志物CA19-9、AFP、CEA、γ-GT联合阳性检出61例,阳性检出率为89.71%,高于单独检测的阳性检出率,差异均有统计学意义(P<0.05)。结论原发性肝癌患者采用化学发光免疫法进行检验后能够取得较高的检验效果,可以为患者的后续治疗提供可靠的依据,值得大力推广。  相似文献   
2.
Alcohol consumption causes significant liver damage, including hepatitis, fibrosis, cirrhosis, and even primary liver carcinoma. Metadoxine (MTDX) is considered to be a beneficial treatment for alcoholic liver disease (ALD) because it accelerates the metabolism and elimination of ethanol. However, the underlying mechanism is not well understood. Here, the rat model of ALD was developed by feeding with 50% ethanol at the dose of 5 g/kg, and samples of serum and liver tissue were collected to test the levels of liver injury and inflammation and evaluate the hepatoprotective function of MTDX in alcohol-induced liver injury. Further investigation on the infiltration of immune cells was performed to understand the potential hepatoprotective mechanism of MTDX in the ALD model. The results showed that MTDX attenuated liver injury, evidenced by decreased levels of alanine transaminase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP). Meanwhile, the liver proinflammatory environment was improved after MTDX treatment, evidenced by decreased levels of TNF-α, IL-6, and NLRP3 in the liver tissue. Furthermore, inhibited infiltrations of macrophages and neutrophils were observed in MTDX-treated ALD rats compared with the untreated ALD rats. Our results indicated that MTDX played an important role in preventing the progression of ALD, and the underlying mechanisms might be related to its function of attenuating liver inflammation by inhibiting immune cell infiltration.  相似文献   
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目的评价新型定量超声(QUS)技术诊断家兔肝纤维化和肝细胞气球样变的价值。方法将30只新西兰大白兔随机分为实验A组(n=12)、实验B组(n=12)及对照组(n=6),以高脂饲料喂养建立兔肝细胞脂肪变性模型;采用剪切波弹性成像(SWE)、剪切波频散成像(SWD)及声衰减成像技术测量相关参数,根据病理学结果判断家兔肝纤维化分期及肝细胞气球样变程度,与超声参数进行比较并分析其相关性。结果实验B组2只家兔死亡,22只模型建立成功,实验A组及B组肝脏均发生不同程度纤维化和肝细胞气球样变。肝纤维化分期是SWV的独立影响因素(P<0.05);F1~3期与F0期家兔剪切波速度(SWV)差异有统计学意义(P<0.05),而F1~2期与F3期差异无统计学意义(P>0.05);肝纤维化分期与SWV呈正相关(r=0.74,P<0.05)。肝细胞气球样变分级是频散值的独立影响因素(P<0.01);B0、B1、B2级肝细胞气球样变家兔频散值两两比较差异均有统计学意义(P均<0.05);肝细胞气球样变分级与频散值呈正相关(r=0.76,P<0.05)。声衰减系数与肝纤维化分期及肝细胞气球样变分级均无显著相关(P均>0.05)。以SWV诊断轻度(≥F1期)和重度纤维化(≥F3期)的曲线下面积(AUC)分别为0.95及0.84;以频散值诊断轻度(≥B1级)和重度肝细胞气球样变(B2级)的AUC分别为0.94及0.87。结论SWE判断家兔肝纤维化分期价值较高;SWE可更好地评估肝细胞气球样变程度。  相似文献   
5.
国医大师徐经世教授在60余年的临床实践中总结提出肝癌的病机为正虚为本,邪实为标;早期多表现为正虚邪实,木旺土虚;病延日久累及下元,则出现水不涵木的病理表现。正虚是该病的病机关键,治疗应遵循“扶正祛邪,分期论治”的治疗原则,病初应“调和中州,培土达木”为主,病至后期则累及下元,治疗则应“滋水涵木,濡养下元”;同时强调饮食生活起居和情志调护,做到精神内守,从而使邪去正安。  相似文献   
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Background– This study intends to address the scarcity of data regarding the pathogenesis of Baclofen poisoning in humans, which has seen a recent increase, worldwide, especially amongst the young people. Another reason for the conduction of this study was lack of the substantial data about the histo-pathological findings of lungs, in synergistic toxicity of Baclofen with Ethanol, in-spite of it being very common in humans, and both being respiratory depressant with similar mechanism of action.Purpose– The authors aimed to understand the pathogenesis of fatal poisonings in humans due to Baclofen in combination with Ethanol via an animal research model. The enhancement of the overall scientific literature by extending research along the lines of the handful studies available in this regard was another adjunct goal of the study.Material and methodsFifteen Wistar rats were divided into control and test group of five and ten subjects respectively. The test group was further divided into two sub-groups of five each, with Baclofen administered to one, and it in conjunction with Ethanol to the other, in lowest dosages adjusted for the humans. Rats in both the groups were euthanized by dislocation of the cervical vertebrae for the histopathology examination.ResultsCapillary and venous plethora, hemorrhages in the inter-alveolar septi, hemorrhages into the alveoli and sludging was seen in the 1st sub-group. The plethora of venules, capillaries and arterioles, with sludging by the WBC (white blood corpuscle) infiltrates was seen in the 2nd sub-group. Desquamation of the ciliated epithelium and edematous thickening of the intra-alveolar septi, along with features suggestive of the peri-vascular edema was seen in the 2nd sub-group. The morphometric analysis of the micro vessels showed a significantly higher value of the arteriolar diameter in the 2nd sub-group, in comparison to 1st, but the venular diameter in the two sub-groups did not differ to any extent.  相似文献   
8.
The microvascular anatomy of the non-lobulated liver of adult Xenopus laevis was studied by scanning electron microscopy of vascular corrosion casts. Hepatic portal veins and hepatic arteries entered hepatic lobes at the hiluses, hepatic veins left at these sites. Intraparenchymal, hepatic portal veins branched up to 10 times before terminal portal venules supplied liver sinusoids. Hepatic arteries closely followed portal vessels. Arteriolar side branches formed anastomoses with close by portal venules (arteriolar-portal anastomoses; APAs), liver sinusoids (arteriolar-sinusoidal anastomoses; ASAs), and peribiliary plexus vessels. Distally, hepatic arteries anastomosed with terminal portal venules having >100 μm in diameter. Liver sinusoids formed a dense three-dimensional network displaying signs of non-sprouting and sprouting angiogenesis evidenced by “holes” and blind ending tapering cast vascular structures (sprouts), respectively. Sinusoids drained via efferent hepatic veins. Right and left hepatic veins drained into the posterior caval vein. Locally, a dense honeycomb-like 3D-meshwork of resin structures was found around terminal portal venules and hepatic arteries. These networks were fed by hepatic arterioles and drained into adjacent terminal portal venules. As their morphologies differed significantly from sinusoids and they were found at sites where diffuse lymphoid tissue is described, we are convinced that they represent the vasculature of diffuse lymphoid tissue areas. Frequencies and diameter ratios of hepatic portal venules versus hepatic arterioles anastomosing with the former (APAs) implicate that the arterial supply contributes to the oxygenation of parenchymal and stromal cells rather than to a significant increase in blood flow towards hepatic sinusoids.  相似文献   
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《Drug discovery today》2022,27(1):280-291
Positron emission tomography (PET) is an extensively used nuclear functional imaging technique, especially for central nervous system (CNS) and oncological disorders. Currently, drug development is a lengthy and costly pursuit. Imaging with PET radiotracers could be an effective way to hasten drug discovery and advancement, because it facilitates the monitoring of key facets, such as receptor occupancy quantification, drug biodistribution, pharmacokinetic (PK) analyses, validation of target engagement, treatment monitoring, and measurement of neurotransmitter concentrations. These parameters demand careful analyses for the robust appraisal of newly formulated drugs during preclinical and clinical trials. In this review, we discuss the usage of PET imaging in radiopharmaceutical development; drug development approaches with PET imaging; and PET developments in oncological and cardiac drug discovery.  相似文献   
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