全文获取类型
收费全文 | 18319篇 |
免费 | 1992篇 |
国内免费 | 1413篇 |
专业分类
耳鼻咽喉 | 141篇 |
儿科学 | 189篇 |
妇产科学 | 256篇 |
基础医学 | 1854篇 |
口腔科学 | 347篇 |
临床医学 | 2355篇 |
内科学 | 3024篇 |
皮肤病学 | 160篇 |
神经病学 | 811篇 |
特种医学 | 555篇 |
外国民族医学 | 6篇 |
外科学 | 1600篇 |
综合类 | 3770篇 |
现状与发展 | 4篇 |
一般理论 | 3篇 |
预防医学 | 1545篇 |
眼科学 | 338篇 |
药学 | 1979篇 |
15篇 | |
中国医学 | 1180篇 |
肿瘤学 | 1592篇 |
出版年
2024年 | 66篇 |
2023年 | 208篇 |
2022年 | 520篇 |
2021年 | 712篇 |
2020年 | 545篇 |
2019年 | 502篇 |
2018年 | 565篇 |
2017年 | 546篇 |
2016年 | 543篇 |
2015年 | 727篇 |
2014年 | 929篇 |
2013年 | 941篇 |
2012年 | 1242篇 |
2011年 | 1310篇 |
2010年 | 944篇 |
2009年 | 828篇 |
2008年 | 933篇 |
2007年 | 1163篇 |
2006年 | 1024篇 |
2005年 | 938篇 |
2004年 | 995篇 |
2003年 | 1177篇 |
2002年 | 1069篇 |
2001年 | 860篇 |
2000年 | 532篇 |
1999年 | 404篇 |
1998年 | 212篇 |
1997年 | 241篇 |
1996年 | 173篇 |
1995年 | 136篇 |
1994年 | 111篇 |
1993年 | 79篇 |
1992年 | 84篇 |
1991年 | 73篇 |
1990年 | 62篇 |
1989年 | 46篇 |
1988年 | 53篇 |
1987年 | 46篇 |
1986年 | 35篇 |
1985年 | 28篇 |
1984年 | 17篇 |
1983年 | 14篇 |
1982年 | 7篇 |
1981年 | 8篇 |
1980年 | 8篇 |
1979年 | 13篇 |
1977年 | 6篇 |
1974年 | 6篇 |
1973年 | 5篇 |
1968年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
陈友芝,主任医师,浙江省著名中医肿瘤与内科专家。出身中医世家,先祖儒医济世,名医辈出,其中有宋代国医陈言,著有《三因极一病证方论》,流芳百世。陈师幼承庭训,立志:“不为良相,即为良医。”青年时代拜江浙名医毛达文先生为师,深得恩师医德医术之精髓。陈师秉家学,承师传,临床 相似文献
992.
目的:比较“杨氏贴棉灸”与激素治疗神经性皮炎的疗效差异。方法:94例局限性皮炎患者,按随机数字表分为2组,治疗组用“杨氏贴棉灸”方法治疗,对照组用醋酸去炎松尿素软膏涂抹,治疗1周后开始观察疗效,持续治疗4周,治疗结束后进行疗效评价。结果:治疗组总有效率95.92%,痊愈率为85.71%;对照组总有效率82.22%,痊愈率为71.11%,两组间比较,经统计学χ2检验,P<0.05,有显著性统计学意义。结论:“杨氏贴棉灸”治疗局限性皮炎疗效显著,可供临床选用。 相似文献
993.
994.
米非司酮合并米索前列醇房事后避孕临床多中心研究 总被引:11,自引:4,他引:11
在黄体早、中、晚期应用米非司酮合并米索前列醇与单用米非司酮进行房事后避孕临床多中心比较性研究。541名自愿接随机序号参加本研究的健康、月经规律妇女,组Ⅰ口服米非司酮25mg,q12h共4次,第三天上午加服米索前列醇0.4mg,妊娠率为0.4%。组Ⅱ单服米非司酮25mg,q12h,共4~6次,妊娠率为3%。二者差异有显著性(P<0.05)。两者引起出血类型和时间均与正常月经相似,且无明显副反应发生,错过了服用传统房事后避孕药时,采用本研究的方法可不考虑性生活时间、次数。这种方法提供了一种新型有效避孕方法。 相似文献
995.
996.
Xiao Ou Shu Mark E. Nesbit Jonathan D. Buckley Mark D. Krailo Leslie L. Robison 《Cancer causes & control : CCC》1995,6(3):187-198
A study of 105 patients with childhood malignant germ-cell tumors (MGCT) and 639 community controls was conducted utilizing a large epidemiologic database collected by the Childrens Cancer Group from 25 member institutions in the United States and Canada. This study was designed to explore the risk factors of this malignancy whose etiology remains poorly understood. A structured, self-administered questionnaire was used to collect exposure information, and data were analyzed using an unconditional logistic regression model with adjustment for relevant confounders. Consistent with the findings from studies of adult MGCT, gestational age was associated inversely with risk of MGCT, with a 70 to 75 percent reduction in risk for children born at term compared with those born pre-term. Parental, particularly maternal, self-reported exposure to chemicals or solvents (odds ratio [OR]=4.6, 95 percent confidence interval [CI]=1.9–11.3) and OR=2.2, CI=1.1–4.7 for maternal and paternal exposure, respectively) and plastic or resin fumes (OR=12.0, CI=1.9–7.5.0 [maternal] and OR=2.5, CI=1.0–6.5 [paternal]) were associated with elevated risk of MGCT. New findings, not reported previously, include a positive relationship of MGCT risk with birthweight and prolonged breastfeeding, an inverse association between MGCT risk and number of cigarettes smoked by the mother during pregnancy, and a 3.1-fold increased risk (CI=1.5–6.6) associated with maternal urinary infections during index pregnancy. Although these findings need confirmation from future studies, they suggest a potential influence of in utero exposure to maternal endogenous hormones, parental environmental exposures, and maternal diseases during pregnancy in the development of childhood MGCT.Drs Shu, Nesbit, and Robison are affiliated with the Department of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, USA. Drs Buckley and Krailo are affiliated with the Department of Preventive Medicine, University of Southern California School of Medicine, Los Angeles, CA, USA. Contributing Childrens Cancer Group Investigators, Institutions, and Grant Numbers are given in the Appendix. Address correspondence to Dr Shu, Childrens Cancer Group, P.O. Box 60012, Arcadia, CA 91066-6012, USA. Grant support is from the US National Cancer Institute and the US Department of Health and Human Services. 相似文献
997.
998.
通过肺癌152例,食管癌82例,手术廓清淋巴结1412个的区域分布和病理结果的比较分析,显示其共性规律是上位癌向上转移大于向下。上叶肺癌转移路近似于“√”号,下叶肺癌转移路似倒“√”号,上段食管癌其梭形转移圈上长下短,下段食管癌则上短下长。 相似文献
999.
药物学研究表明诱导肿瘤细胞程序死亡/凋亡(apoptosis)可能是许多化疗药物杀伤肿瘤细胞的机制之一,细胞凋亡与细胞坏死有本质区别,凋亡的特征有质膜保持完整性,核染色质固缩,内源性核酸内切酶激活将染色质DNA降解成寡聚核小体,电泳带谱表现为特征性梯状带。榄香烯(elemene)系我国自行研制的抗癌新药。 相似文献
1000.
Singh J Van Vlijmen H Liao Y Lee WC Cornebise M Harris M Shu IH Gill A Cuervo JH Abraham WM Adams SP 《Journal of medicinal chemistry》2002,45(14):2988-2993
The antigen alpha4beta1 (very late antigen-4, VLA-4) plays an important role in the migration of white blood cells to sites of inflammation. It has been implicated in the pathology of a variety of diseases including asthma, multiple sclerosis, and rheumatoid arthritis. We describe a series of potent inhibitors of alpha4beta1 that were discovered using computational screening for replacements of the peptide region of an existing tetrapeptide-based alpha4beta1 inhibitor (1; 4-[N'-(2-methylphenyl)ureido]phenylacetyl-Leu-Asp-Val) derived from fibronectin. The search query was constructed using a model of 1 that was based upon the X-ray conformation of the related integrin-binding region of vascular cell adhesion molecule-1 (VCAM-1). The 3D search query consisted of the N-terminal cap and the carboxyl side chain of 1 because, upon the basis of existing structure-activity data on this series, these were known to be critical for high-affinity binding to alpha4beta1. The computational screen identified 12 reagents from a virtual library of 8624 molecules as satisfying the model and our synthetic filters. All of the synthesized compounds tested inhibit alpha4beta1 association with VCAM-1, with the most potent compound having an IC(50) of 1 nM, comparable to the starting compound. Using CATALYST, a 3D QSAR was generated that rationalizes the variation in activities of these alpha4beta1 antagonists. The most potent compound was evaluated in a sheep model of asthma, and a 30 mg nebulized dose was able to inhibit early and late airway responses in allergic sheep following antigen challenge and prevented the development of nonspecific airway hyperresponsiveness to carbachol. Our results demonstrate that it is possible to rapidly identify nonpeptidic replacements of integrin peptide antagonists. This approach should be useful in identification of nonpeptidic alpha4beta1 inhibitors with improved pharmacokinetic properties relative to their peptidic counterparts. 相似文献