全文获取类型
收费全文 | 13032篇 |
免费 | 878篇 |
国内免费 | 130篇 |
专业分类
耳鼻咽喉 | 18篇 |
儿科学 | 148篇 |
妇产科学 | 48篇 |
基础医学 | 567篇 |
口腔科学 | 22篇 |
临床医学 | 2875篇 |
内科学 | 1942篇 |
皮肤病学 | 29篇 |
神经病学 | 3221篇 |
特种医学 | 400篇 |
外科学 | 379篇 |
综合类 | 1553篇 |
预防医学 | 832篇 |
眼科学 | 22篇 |
药学 | 631篇 |
5篇 | |
中国医学 | 1313篇 |
肿瘤学 | 35篇 |
出版年
2024年 | 24篇 |
2023年 | 245篇 |
2022年 | 525篇 |
2021年 | 741篇 |
2020年 | 709篇 |
2019年 | 683篇 |
2018年 | 690篇 |
2017年 | 641篇 |
2016年 | 570篇 |
2015年 | 454篇 |
2014年 | 1225篇 |
2013年 | 1253篇 |
2012年 | 877篇 |
2011年 | 897篇 |
2010年 | 671篇 |
2009年 | 587篇 |
2008年 | 512篇 |
2007年 | 479篇 |
2006年 | 415篇 |
2005年 | 316篇 |
2004年 | 242篇 |
2003年 | 210篇 |
2002年 | 152篇 |
2001年 | 131篇 |
2000年 | 90篇 |
1999年 | 100篇 |
1998年 | 72篇 |
1997年 | 74篇 |
1996年 | 47篇 |
1995年 | 68篇 |
1994年 | 48篇 |
1993年 | 40篇 |
1992年 | 41篇 |
1991年 | 23篇 |
1990年 | 30篇 |
1989年 | 27篇 |
1988年 | 12篇 |
1987年 | 13篇 |
1986年 | 16篇 |
1985年 | 25篇 |
1984年 | 12篇 |
1983年 | 8篇 |
1982年 | 5篇 |
1981年 | 9篇 |
1980年 | 4篇 |
1979年 | 9篇 |
1978年 | 7篇 |
1977年 | 4篇 |
1976年 | 5篇 |
1971年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
Summary Percutaneous angioplasty is a well-established method of treating arterial stenoses and occlusions in various regions. In the carotid area this technique is still under discussion. The successful application of angioplasty in eight patients with carotid artery stenoses is reported.Adapted from a paper presented at XII European Congress for Neuroradiology in Prague, 27–29 September, 1984 相似文献
52.
采用Barthel指数对120例脑卒中住院患者在发病后5 ̄6周进行日常生活活动(ADL)能力的证实。因脑卒中遗留的功能不全,ADL的受损率达66.7%,肢体的Brunnstrom功能分级与ADL积分高度相关,相关性下肢高于上肢;多元逐步回归分析显示,躯体(偏瘫)和心理(认知障碍和抑郁因素)影响ADL的能力。认为ADL能力的提高,不仅依赖于肢体功能障碍的改善,提高认知功能,改善情感状况,对于脑卒中患 相似文献
53.
54.
55.
脑卒中与继发性癫癎 总被引:9,自引:0,他引:9
目的:探讨首发脑卒中患者继发性癫癎的发病率、发病时间与脑卒中病变部位的关系。方法:回顾性分析经我院近3年来治疗的659例首发脑卒中住院患者的临床资料。结果:首发脑卒中患者继发癫癎发生率为8.19%(54/659)。癫癎发作与卒中病变部位有关,累及皮层或邻近皮层者易继发癫癎(53.33%,24/45)。54例继发癫癎中68.52%为早发性癫癎(起病后2周内),余31.48%为晚发性癫癎(起病2周以后)。以脑出血继发早发性癫癎为主(81.25%,13/16);脑梗死则易发生晚发性癫癎(60.00%,12/20)。结论:分析首发卒中后癫癎的发病特点有助于指导临床治疗。 相似文献
56.
57.
Ghaus M. Malik Balaji Sadasivan Robert S. Knighton James I. Ausman 《Child's nervous system》1991,7(1):43-47
Between January 1941 and June 1989, 46 children below the age of 18 with an arteriovenous malformation (AVM) were managed. There were 7 patients with AVM diagnosed before the age of 2; 10 patients were diagnosed between the ages of 3 and 10; and 29 patients were diagnosed between 11 and 18. There were equal numbers of male and female patients. Twenty-five of the AVMs were large (>5 cm longest diameter). All 7 AVMs diagnosed before the age of 2 were large. The usual clinical presentation was congestive heart failure, bruit and an enlarging head. Three patients underwent excision with 2 deaths and 1 excellent result. In 11 patients (aged 3–18) with AVM without history of hemorrhage, 3 had excision with 2 excellent and 1 fair result. Four remained stable. Four developed progressive deficits or hemorrhage. In 10 patients (aged 3–18) with AVM and hemorrhage who were treated medically, 7 (70%) had an episode of re-hemorrhage. Three patients had excision of AVM after re-hemorrhage, but before the age of 18 with an excellent result. Eighteen patients (aged 3–18) with AVM and a single episode of hemorrhage underwent excision with 17 excellent or good results and 1 fair result. The overall mortality was 7%. Eighty-five percent of the children with excision of AVM had an excellent or good result. The best treatment for AVM in children is surgical excision.Presented at the XVII Annual Meeting of the International Society for Pediatric Neurosurgery, Bombay 1989 相似文献
58.
R. Grant Steen Wilburn E. Reddick Raymond K. Mulhern James W. Langston Robert J. Ogg Andrea A. Bieberich Peter B. Kingsley Winfred C. Wang 《Journal of magnetic resonance imaging : JMRI》1998,8(3):535-543
Conventional MRI (cMRI) has shown that brain abnormalities without clinical stroke can manifest in patients with sickle cell disease (SCD). We used quantitative MRI (qMRI) and psychometric testing to determine whether brain abnormalities can also be present in patients with SCD who appear normal on cMRI. Patients 4 years of age and older with no clinical evidence of stroke were stratified by cMRI as normal (n = 17) or abnormal (n = 13). Spin-lattice relaxation time (T1) of gray and white matter structures was measured by the precise and accurate inversion recovery (PAIR) qMRI method. Patient cognitive ability was assessed with a standard psychometric instrument (WISC-III or WISC-R). In all 30 patients with SCD, qMRI T1 was lower than in 24 age- and race-matched controls, in cortical gray matter (P < .0006) and caudate (P < .0009), as well as in the ratio of gray-to-white matter T1 (P < .008). In the 17 patients who were shown to be normal by cMRI, qMRI T1 was still lower than in controls, in both cortical gray matter (P < .02) and caudate (P < .004). Histograms of voxel T1 show that the proportion of voxels with T1 values intermediate between gray and white matter (ie, consistent with encephalomalacia) was 9% higher than controls in patients shown to be normal by cMRI (P < .05) and 15% higher than controls in patients shown to be abnormal by cMRI (P < .0005). The full scale intelligence quotient (FSIQ) of all patients with SCD was 75, compared to the FSIQ of 88 in a historical control group of patient siblings (P < .001). The FSIQ of patients shown to be normal by cMRI was 79, significantly lower than the FSIQ of patient siblings (P < .04). The FSIQ of 71 in patients shown to be abnormal by cMRI was significantly lower than both the patient siblings (P < .005) and the patients shown to be normal by cMRI (P < .04). Patients shown to be abnormal by cMRI scored lower than patients shown to be normal by cMRI, specifically on the subtests of vocabulary (P = .003) and information (P = .03). Cognitive impairment is thus significant, even in patients with SCD who were shown to be normal by cMRI, suggesting that cMRI may be insensitive to subtle neurologic damage that can be detected by qMRI. Because cognitive impairment can occur in children normal by cMRI, our findings imply that prophylactic therapy may be needed earlier in the course of SCD to mitigate neurologic damage. 相似文献
59.
脑卒中后认知障碍(PSCI)是脑卒中患者常见的并发症,严重影响患者的生活质量。目前,PSCI在临床治疗中尚未发现有效的针对性治疗措施。大量研究证实核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)炎症小体的活化在PSCI中起关键作用,且对其进行的许多抑制性治疗显示出了改善认知障碍的功效。为此,本文总结了NLRP3炎症小体的活化和影响因素及其与PSCI的关系,发现在PSCI的细胞和动物模型中,针对NLRP3或其炎症小体成分的抑制措施可以减轻炎性反应和相应的病理特征,从而促进其认知功能的恢复,因此,靶向NLRP3炎症小体可能是PSCI治疗的新趋势。然而到目前为止,尽管许多药物和治疗措施已成功鉴定出能够抑制NLRP3炎症小体的活化,但其在临床中的治疗效果和安全性仍有待进一步验证。 相似文献
60.
背景 血栓栓塞(TE)事件是肥厚型心肌病(HCM)的重要并发症。目前针对HCM患者TE事件的风险预测,仅国外学者构建了两个模型:HCM Risk-CVA及French HCM score,然而,现有研究发现HCM Risk-CVA模型对于中国HCM患者的临床价值较为有限。目的 本研究拟构建适合中国HCM患者的TE事件风险预测模型。方法本研究系回顾性队列研究,收集2010—2018年在四川大学华西医院就诊的537例HCM患者的病例资料。本研究通过电话随访或电子病历系统查询患者就诊记录,每6~12个月随访1次,直至出现终点事件或死亡或研究拟定的评估日期(2019-12-31),终点事件定义为复合性TE事件。采用单因素和多因素Cox回归分析构建风险预测模型,并使用自助重抽样的方法进行内部验证。结果 537例患者中,24例患者有不同程度的数据缺失,最终纳入513例患者。中位随访时间为4.2(1.3,6.2)年,随访过程中42例(8.18%)发生TE事件,年发病率为2.10%[95%CI(1.47%,2.73%)]。根据多因素Cox回归模型构建TE事件风险预测模型,最终纳入年龄、既往TE事件、心... 相似文献