全文获取类型
收费全文 | 2745篇 |
免费 | 284篇 |
国内免费 | 140篇 |
专业分类
耳鼻咽喉 | 3篇 |
儿科学 | 4篇 |
妇产科学 | 55篇 |
基础医学 | 51篇 |
口腔科学 | 6篇 |
临床医学 | 102篇 |
内科学 | 141篇 |
皮肤病学 | 19篇 |
神经病学 | 16篇 |
特种医学 | 12篇 |
外科学 | 65篇 |
综合类 | 607篇 |
预防医学 | 116篇 |
眼科学 | 13篇 |
药学 | 617篇 |
5篇 | |
中国医学 | 1324篇 |
肿瘤学 | 13篇 |
出版年
2024年 | 14篇 |
2023年 | 32篇 |
2022年 | 63篇 |
2021年 | 105篇 |
2020年 | 107篇 |
2019年 | 56篇 |
2018年 | 73篇 |
2017年 | 118篇 |
2016年 | 129篇 |
2015年 | 101篇 |
2014年 | 306篇 |
2013年 | 243篇 |
2012年 | 283篇 |
2011年 | 258篇 |
2010年 | 198篇 |
2009年 | 128篇 |
2008年 | 133篇 |
2007年 | 139篇 |
2006年 | 140篇 |
2005年 | 86篇 |
2004年 | 89篇 |
2003年 | 84篇 |
2002年 | 57篇 |
2001年 | 48篇 |
2000年 | 40篇 |
1999年 | 27篇 |
1998年 | 22篇 |
1997年 | 16篇 |
1996年 | 11篇 |
1995年 | 11篇 |
1994年 | 11篇 |
1993年 | 5篇 |
1992年 | 9篇 |
1991年 | 4篇 |
1990年 | 4篇 |
1989年 | 4篇 |
1988年 | 3篇 |
1987年 | 3篇 |
1986年 | 2篇 |
1985年 | 4篇 |
1983年 | 1篇 |
1979年 | 1篇 |
1976年 | 1篇 |
排序方式: 共有3169条查询结果,搜索用时 0 毫秒
1.
2.
3.
复方丹参滴丸对急慢性高粘滞血症模型血管内皮细胞分泌功能的影响 总被引:5,自引:0,他引:5
目的:观察复方丹参滴丸对高粘滞血症血管内皮分泌功能的影响,探索其作用机制。方法:复合因素(高分子右旋糖酐、肾上腺素、牛血清白蛋白)、长时间(112天)造成高粘滞血症慢性模型;一次性静脉注射高分子右旋糖酐。皮下注射(sc)肾上腺素造成急性高粘滞血症模型,分别用复方丹参滴丸进行治疗,观察血管肉皮细胞分泌功能的变化。结果:慢性高粘滞血症模型血浆血栓素B2(TXB2)和内皮素(ET)浓度非常显升高,而6-酮-前列腺素F1x(6-酮)浓度非常显降低;急性高粘滞血症模型血管内皮分泌功能无显变化;长期使用复方丹参滴丸能调整、改善血管内皮分泌功能的异常状态;复方丹参滴丸改善血管内皮分泌功能的即时效应不显。 相似文献
4.
Many women find the idea of a once-a-month contraceptive pill an attractive concept. Mifepristone has been shown to be effective as a contraceptive if administered in the early luteal phase. We tested the contraceptive efficacy of 200 mg of mifepristone on day luteinizing hormone (LH) + 2 in a group of 32 women who used a fertility monitor to identify the LH surge. We also recruited a control group, comprising 20 women who were trying to conceive. In this group, 12 women conceived during a total of 50 control cycles (probability of pregnancy 0.25-0.32). Women in the treatment group contributed to a total of 178 cycles and there were two pregnancies (probability of pregnancy 0.01). An LH surge was not detected in 34 cycles (19.1%). In 20 cycles (11.2%) this was due to imperfect use while 14 were monitor method failures (7.9%). Treatment with mifepristone in the early luteal phase did not disrupt the cycle length but women reported slight vaginal bleeding in 15% of the cycles. The combination of a home-use fertility monitor with once-a-month administration of mifepristone (especially if mifepristone is administered at the early luteal phase) is an acceptable contraceptive option with minimal side effects. Unfortunately, it is difficult to envisage how an easier way of defining the correct timing, which required less compliance, could be devised. 相似文献
5.
目的 基于中医药整合药理学和转录组学探究丹栀逍遥散防治焦虑肝郁化火证的作用机制。方法 采用中医药整合药理学研究平台v2.0,检索并获取丹栀逍遥散的活性成分及靶标、焦虑肝郁化火证靶标信息,构建中药-成分-靶点-通路网络。将交集基因导入String数据库,构建交集靶点的蛋白互作网络,以确定最终需要验证的靶标。利用GEO数据库转录组学验证整合网络药理学结果,同时采用动物实验进行验证。结果 共筛选出与焦虑肝郁化火证相关的靶标13个,丹栀逍遥散活性成分430种。整合药理学结果显示,丹栀逍遥散防治焦虑肝郁化火证主要通过调控α-氨基-3-羟基-5-甲基-4-异噁唑丙酸受体(α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor,AMPAR)、蛋白激酶A(protein kinase A,PKA)、N-甲基-D-天冬氨酸(N-methyl-D-aspartic acid,NMDA)受体的激活及磷脂酰肌醇3-激酶(phosphatidylinositide 3-kinases,PI3K)/蛋白激酶B(protein kinase B,... 相似文献
6.
目的:评价六味地黄汤联合逍遥散加减治疗肾虚肝郁型围绝经期睡眠障碍的有效性和安全性。方法:受试者随机分为两组,试验组予六味地黄汤联合逍遥散加减口服;对照组予戊酸雌二醇联合地屈孕酮序贯口服。试验组以30 d为1个疗程,对照组以21 d为1个疗程,连续治疗3个疗程。观察两组治疗前后PSQI评分、Kupperman评分、中医证候积分、血清FSH、E2及血尿常规、肝肾功和心电图等指标的变化。结果:试验组总有效率93.3%,对照组90.0%;两组均能明显降低PSQI、改良Kupperman和中医证候评分,在改善中医证候积分方面试验组明显优于对照组,差异有统计学意义(P<0.01)。对照组在减低Kupperman评分上优于试验组,差异有统计学意义(P<0.01)。两组对血清FSH水平均有下调趋势,均可上调血清E2水平,对照组较试验组对血清E2上调更明显(P<0.01)。结论:六味地黄汤联合逍遥散加减治疗肾虚肝郁型围绝经期睡眠障碍安全有效。 相似文献
7.
8.
Furedi A 《Human reproduction update》1999,5(6):621-626
The warning issued by the UK Committee on Safety Medicines in October 1995, followed by their 'Dear Doctor' letter of October 18, 1995, that oral contraceptive pills containing gestodene or desogestrel were associated with a higher risk of venous thromboembolism has had a negative impact on public heath. A significant number of women either switched brands or ceased contraception altogether following the announcement. National data suggest a strong association between the pill scare and a substantial increase in the number of unintended pregnancies, particularly significant among younger women, with use of oral contraception falling from 40 to 27% of under 16s between 1995-1996 and 1996-1997. The resulting cost of the increase in births and abortions to the National Health Service has been estimated at about Pound Sterling 21 million for maternity care and from Pound Sterling 46 million for abortion provision. The level of risk should, in future, be more carefully assessed and advice more carefully presented in the interests of public health. 相似文献
9.
The relatively short history of hormonal contraception has been marked by a series of 'pill scares', all of which--after creating panic among users--were proven to be unfounded in terms of public health impact. The latest pill scare, provoked by regulatory action in the United Kingdom and the Federal Republic of Germany in response to the publication of a series of articles indicating a doubling of risk of deep venous thrombosis in users of oral contraceptives containing third-generation progestins, seems finally settled: both the British and the German Drug Regulatory Authorities have now reverted their verdict. The damage unfortunately stays: hundreds of thousands of women have been compelled to abandon the pill of their choice, often deciding to drop contraception altogether, thereby exposing themselves to unwanted pregnancy and--in a number of cases--to pregnancy termination. This latest episode should be turned into something positive: we need to learn that, in the case of drugs in widespread use, before restrictive action is taken--and except for very rare and specific instances--the scientific community must carry out an exhaustive debate on the reality and importance of the observed effects. Although the public should, in each instance, be properly informed, it is only after this process has been completed that restrictive action should be taken. It is hoped that, after this last episode, all concerned have learned this simple principle and will accept being guided by it from now on. 相似文献
10.
复方软伤伸筋丸治疗膝关节骨性关节炎临床研究 总被引:7,自引:0,他引:7
周成刚 《中国中医骨伤科杂志》2003,11(3):5-7
目的 :探讨复方软伤伸筋丸治疗膝关节骨性关节炎的疗效机理。方法 :采用单盲法将膝关节骨性关节炎患者 2 2 0例 ,随机分为软伤伸筋丸组 (治疗组 ) 1 60例 ,壮骨关节丸组 (对照组 ) 60例 ,对比分析两组临床疗效。结果 :1治疗组临床治愈率为 88.75 % ,总有效率为 99.3 5 % ;对照组临床治愈率为 2 3 .3 3 % ,总有效率为 91 .68% ,治疗组优于对照组 ,具有显著性差异 (P<0 .0 1 )。2复方软伤伸筋丸无毒副作用。3复方软伤伸筋丸的应用可使增生骨刺吸收 ,损伤半月板修复。结论 :复方软伤伸筋丸是一种治疗膝关节骨性关节炎安全有效药物。 相似文献