首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   75669篇
  免费   6155篇
  国内免费   1173篇
耳鼻咽喉   386篇
儿科学   1155篇
妇产科学   1498篇
基础医学   3223篇
口腔科学   2016篇
临床医学   19836篇
内科学   5766篇
皮肤病学   376篇
神经病学   4277篇
特种医学   1566篇
外国民族医学   6篇
外科学   10251篇
综合类   9644篇
现状与发展   3篇
一般理论   6篇
预防医学   12130篇
眼科学   303篇
药学   6199篇
  171篇
中国医学   2530篇
肿瘤学   1655篇
  2024年   193篇
  2023年   1658篇
  2022年   2821篇
  2021年   3884篇
  2020年   4326篇
  2019年   3319篇
  2018年   3095篇
  2017年   3107篇
  2016年   2979篇
  2015年   2898篇
  2014年   6331篇
  2013年   6556篇
  2012年   4910篇
  2011年   5087篇
  2010年   4163篇
  2009年   3625篇
  2008年   3832篇
  2007年   3308篇
  2006年   3028篇
  2005年   2349篇
  2004年   2013篇
  2003年   1595篇
  2002年   1221篇
  2001年   1001篇
  2000年   812篇
  1999年   718篇
  1998年   619篇
  1997年   533篇
  1996年   417篇
  1995年   343篇
  1994年   319篇
  1993年   270篇
  1992年   241篇
  1991年   209篇
  1990年   124篇
  1989年   134篇
  1988年   116篇
  1987年   118篇
  1986年   114篇
  1985年   130篇
  1984年   96篇
  1983年   81篇
  1982年   79篇
  1981年   68篇
  1980年   53篇
  1979年   27篇
  1978年   22篇
  1977年   14篇
  1976年   19篇
  1975年   12篇
排序方式: 共有10000条查询结果,搜索用时 46 毫秒
111.
研究生科学道德和学风建设是学位与研究生教育的重要组成部分。针对近年来科学研究和学术活动中各种违背科学道德和学术规范的行为时有发生,国家教育部对研究生科学道德和学风建设日益重视,因此构建研究生的科学道德和学风教育质量管理体系具有十分重要的意义。实现研究生科学道德和学风教育质量体系的方针和目标需具备三个要素,即教育实践的模式(集主题教育、方法学习、学术实践三位一体)、有效性评价机制和绩效考核机制。此外,尚需建立体系优化机制,以适应各种内外部因素的变化,保持体系的更新和优化。  相似文献   
112.
113.
目的 评价缺血修饰性白蛋白(ischemia modified albumin,IMA)对急性缺血性胸痛(ICP)的早期诊断价值。方法 时206例发病〈12h、表现为急性胸痛的患者立即行12导联心电图(ECG)检查,并抽血进行IMA、肌钙蛋白I(cTnI)、肌酸激酶同工酶MB(CK-MB)测定。将ECG、IMA、cTnI、CK-MB的结果单独或结合与最终诊断为非缺血性胸痛(NICP)及ICP的相互关系进行比较。结果 最后诊断为ICP98例,NICP108例,ICP发病〈3h和3-6h组IMA水平明显升高,与NICP组比较差异有统计学意义(P〈0.001);ICP发病〉6h组IMA水平与NICP组比较差异无统计学意义(P〉0.05)。IMA诊断发病〈3hICP的敏感性和阴性预测值(NPV)为89.1%和88.8%,明显高于ECG、cTnI和CK-MB,四者结合为97.6%和96.9%;IMA诊断发病3~6hICP的敏感性和NPV为71.7%和74.5%,也高于ECG、cTnI、CK-MB,四者结合为95.5%和94.2%;但IMA对于发病〉6h的ICP则无诊断作用。结论 IMA是诊断ICP的早期敏感生化指标,对于发病〈6h(尤其是〈3h)的ICP诊断具有较高的敏感性和NPV,优于ECG、CK-MB、cTnI;将IMA与其他指标结合,可进一步提高对ICP的诊断价值。  相似文献   
114.
Objective To investigate the relationship between degree of endometrioma adhesions and clinical feature, surgical treatment and postoperative recurrence. Methods From Jan 2003 to Mar 2008, 662 patients with endometrioma undergoing laparoscopic ovarian endometrioma excision in Peking Union Medical College Hospital were studied retrospectively. All patients were classified into four groups according to the extent of adhesions: 31 cases in none adhesions group, 123 cases in mild adhesions group (filmy thickness, avascular, easily separated adhesions), 310 cases in moderate adhesions group (less than a half of ovary was adjacent to dense thickness adhesions which was difficult to separate, or above a half of ovary were adjacent to filmy thickness adhesions) and 198 cases in severe adhesions group (above a half of ovary was adjacent to dense thickness, well vascularized adhesions which was difficult to separate, and always involved the other pelvic organs, observed angiogenesis). The comparison of degree, characteristics, period of pain, lab test, surgical management and postoperative recurrence was performed among those above groups. In the mean time, risk factors and multinomial logistic regression were analyzed. Results (1)Clinical characteristics: The incidence of patients with dysmenorrhea, dyspareunia, straining feeling in anus, chronic pelvic pain and the level of CA125 (>35 kU/L) was remarkably higher in moderate-to-severe adhesion groups than in none-to-mild adhesions groups (P=0.000, 0.000, 0.001, 0.006 and 0.000, respectively). Infertility rate were significantly higher in severe adhesions group(15.7%,31/198) than none adhesions group(3.2%,1/31), mild adhesions group(11.4%,14/123) and moderate adhesions group(9.7%,30/310, OR=1.728, P<0.05).(2)Operating time and blood loss: Operating time of each groups was as followed: (37±15) min in none adhesions group, (42±19) min in mild adhesions group, (50±20) min in moderate adhesions group and (63±22) min in severe adhesion group. Blood loss was (23±12) ml in none adhesion group, (31±27) ml in mild adhesion group, (40±32) ml in moderate adhesion group and (70±67) ml in severe adhesions group. Thicker adhesions result in longer operation time and more blood loss. (3)Combined with other disease: The ratio of patients who combined with adenomyosis or deeply infiltrating endometriosis in moderate-to-severer adhesion groups was higher than patients in none-to-mild adhesions groups (OR=3.466, P=0.000). (4) Postoperative recurrence: It was categorized into recurrence of pain and cyst. Moderate-to-severe adhesions was related to higher recurrence rate of pain (OR=1.685,P=0.046), but was irrelevant to recurrence of cyst. Conclusion The more extent of endometrioma adhesions was related to severer pelvic pain symptoms, longer operating time and more blood loss. Postoperative pain recurrence rate was observed in moderate-to-severe adhesion group. Extent of adhesions was irrelevant to cyst recurrence.  相似文献   
115.
116.
Spinal cord stimulation (SCS) is widely used for pain relief in patients with failed back surgery syndrome (FBSS), and muscle weakness is a common finding in patients with chronic pain. We present here a single case report of a 47‐year‐old woman, who, after SCS for FBSS, had continuous improvement in lower leg muscle strength and gait, but only transient and minimal pain relief. To the authors’ knowledge, this is only the second published case report of significant improvement in “motor” function, independent of the analgesic effect following SCS in FBSS. If SCS, in fact, does improve muscle strength, new strategies for the management of patients with chronic pain might be opened up. Further studies are needed to verify this hypothesis.  相似文献   
117.
医疗设备维修管理之团队建设   总被引:3,自引:3,他引:0  
通过我院设备科设备维修队伍的团队建设,说明团队建设在设备维修管理中的重要性。  相似文献   
118.
The results of lumbar fusion in chronic low back pain (LBP) patients vary considerably, and there is a need for proper patient selection. Lumbosacral orthoses have been widely used to predict outcome, however, with little scientific support. The aim of the present study was to determine the value of a pantaloon cast test in selecting chronic LBP patients for lumbar fusion or conservative management. First, a systematic review of the literature was carried out in which two independent reviewers identified studies in Medline, Cochrane and Current Contents databases. Three papers met the selection criteria. In the only study with a control group, a significantly better outcome after fusion compared to conservative treatment was found in patients who reported significant pain relief while in a cast (i.e. a positive cast test). The results of lumbar fusion, however, were not significantly different for patients with a positive and those with a negative cast test. In addition to the review, a clinical cohort study of 257 LBP patients, who had been allocated to either lumbar fusion or conservative management by a temporary external transpedicular fixation trial, was performed. Prior to allocation, all had undergone a pantaloon cast test. Patients with no history of prior spine surgery and with a positive pantaloon cast test had a better outcome after lumbar fusion than those treated conservatively (P = 0.002, χ 2 test). In patients with previous spine operations the outcomes were poor and the test was of no value. From the literature and the present patient cohort, it was concluded that only in chronic LBP patients without prior spine surgery, a pantaloon cast test with substantial pain relief suggests a favorable outcome of lumbar fusion compared to conservative management. The test has no value in patients who have had previous spine surgery.  相似文献   
119.
加强医疗仪器设备管理提高医疗仪器设备使用效益   总被引:1,自引:0,他引:1  
加强医疗设备管理,提高设备使用效益,制定合理的计划,正确选购设备,为医院提供品种、性能、精度适当的技术装备。  相似文献   
120.
目的探讨氦氖激光血液照射辅助治疗控制癌痛的疗效。方法对52例中晚期癌症重度痛患者在使用口服吗啡治疗基础上加用低能量氦氖激光血液照射治疗1周后,对疼痛缓解程度及平均缓解时间进行对照观察。结果加用激光照射组的镇痛疗效优于单用吗啡组,P<0.05,有效率分别为92%和84%,P>0.05,显效率分别为67%和46%,u=2.07,P<0.05,均数缓解时间分别为(8±3)h和(8±4)h,t=0.78,P>0.05,差异无显著性意义。结论氦氖激光血液照射治疗有一定协同镇痛作用。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号