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   2691篇
  免费   418篇
  国内免费   76篇
耳鼻咽喉   19篇
儿科学   74篇
妇产科学   78篇
基础医学   440篇
口腔科学   32篇
临床医学   213篇
内科学   299篇
皮肤病学   27篇
神经病学   162篇
特种医学   116篇
外国民族医学   2篇
外科学   385篇
综合类   288篇
预防医学   153篇
眼科学   12篇
药学   136篇
  3篇
中国医学   114篇
肿瘤学   632篇
  2024年   5篇
  2023年   40篇
  2022年   71篇
  2021年   173篇
  2020年   158篇
  2019年   149篇
  2018年   161篇
  2017年   139篇
  2016年   157篇
  2015年   134篇
  2014年   227篇
  2013年   214篇
  2012年   169篇
  2011年   149篇
  2010年   135篇
  2009年   122篇
  2008年   152篇
  2007年   108篇
  2006年   110篇
  2005年   82篇
  2004年   61篇
  2003年   50篇
  2002年   60篇
  2001年   46篇
  2000年   33篇
  1999年   33篇
  1998年   28篇
  1997年   35篇
  1996年   27篇
  1995年   20篇
  1994年   24篇
  1993年   12篇
  1992年   16篇
  1991年   16篇
  1990年   10篇
  1989年   10篇
  1988年   8篇
  1987年   8篇
  1986年   6篇
  1985年   5篇
  1984年   5篇
  1983年   6篇
  1982年   5篇
  1981年   1篇
  1980年   3篇
  1978年   1篇
  1975年   1篇
排序方式: 共有3185条查询结果,搜索用时 343 毫秒
91.
We evaluated p53, KRAS, BRAF and CTNNB1 mutation and p53, WT1, p16 and beta‐catenin expression in 31 ovarian high‐grade serous adenocarcinoma. Twenty‐five (80.6%) tumors contained functional mutations of p53; three frameshift, four nonsense and 19 missense mutations. None of the tumors showed KRAS, BRAF or CTNNB1 mutation. In all 18 tumors with missense mutations, ≥60% of tumor cells were strongly positive for p53 immunostaining whereas all tumors with frameshift or nonsense mutations were completely negative. Missense mutation was correlated with diffuse and strong imunoreaction and frameshift/nonsense mutation was correlated with completely negative immunoreaction (P = 0.000). Tumors with wild‐type p53 revealed a wide range of immunostaining patterns. In 27 (87.1%) and 18 (58.1%) tumors, ≥50% of tumor cells were moderate to strongly positive for WT1 and p16, respectively. A considerable intratumoral heterogeneity for p16 expression was present. None of the tumors demonstrated nuclear beta‐catenin expression. p53 mutations appear to be a powerful molecular marker for ovarian high‐grade serous adenocarcinoma. Using p53 with an appropriate interpretation criteria together with WT1, p16 and beta‐catenin, most of the high‐grade serous adenocarcinoma could be distinguished from other ovarian tumors.  相似文献   
92.
李洁  商锟鹏  卢彪 《全科护理》2021,19(13):1786-1789
目的:探究基于GRACE评分系统的临床分级护理在急性冠状动脉综合征(ACS)胸痛病人中的应用效果。方法:选取2017年12月—2019年12月医院就诊的70例ACS胸痛病人为研究对象,随机分为观察组与对照组各35例。对照组实施常规护理,观察组实施基于GRACE评分系统的临床分级护理。比较两组病人不良心血管事件(MACE)、死亡情况以及护理质量状况。结果:观察组病人MACE总发生率及病死率明显低于对照组(P<0.05);观察组病人直接护理时间明显长于对照组,分级护理合格率、护理措施到位率明显高于对照组,住院时间明显短于对照组(P<0.05)。结论:基于GRACE评分系统的临床分级护理应用于ACS胸痛病人中,可明显减少MACE发生风险,降低病死率,提高护理质量。  相似文献   
93.
目的:调查河北省急性缺血性脑卒中患者的院内诊治时间分布情况。方法:收集并分析河北省急性缺血性脑卒中患者的院内诊治流程资料并与NINDS推荐时间进行比较。结果:院内诊治中位时间104 min高于推荐的60 min( P<0.001);"完成头颅CT扫描-获取CT报告"中位时间30 min高于推荐的20 min( P<0.001);"获取头颅CT报告-开始治疗"中位时间43 min高于推荐的15 min( P<0.001)。通过EMS就诊患者院内诊治中位时间是101 min,低于未采用患者的104 min( P=0.01);三级医院院内诊治中位时间是105 min,迟于二级医院的99 min ( P<0.05)。 结论:河北省急性缺血性脑卒中院内救治延迟现象严重。获取头颅CT报告到开始溶栓治疗这一环节是造成院内延迟的最主要环节。通过EMS就诊可以缩短院内救治时间;二级医院相比三级医院院内延迟情况较轻。  相似文献   
94.
95.
96.
97.
98.
AIMS: Prior studies suggest that acute coronary syndromes (ACSs) are associated with endothelial activation and that this is of prognostic significance. We hypothesized that endothelial activation, as measured by a rise in von Willebrand Factor (DeltavWF), was influenced by the thrombolysis in myocardial infarction flow grade (TFG), the corrected TIMI frame count (CTFC) and the choice of anticoagulant therapy after fibrinolysis in ST elevation myocardial infarction (STEMI). METHODS AND RESULTS: Data were drawn from the enoxaparin and tenecteplase tissue plasminogen activator (TNK-tpa) with or without GPIIb/IIIa inhibitor as the reperfusion strategy in the STEMI trial (ENTIRE-TIMI 23). Three hundred and fourteen patients had serial measurements of vWF (baseline and 48-72 h) and angiographic data available. TFG<3 (P=0.0042) or CTFC>/=40 at 60 min (P=0.0035) were associated with a higher DeltavWF. DeltavWF >/=75th percentile was associated with a higher incidence of death or myocardial infarction (MI) at 30 days, compared with <75th percentile (11.2 vs. 4.1%, P=0.027). Enoxaparin independently reduced the DeltavWF (P=0.019) and also the composite of death or MI (OR 0.33, 95% CI 0.12-0.91, P=0.03) compared with unfractionated heparin. CONCLUSION: In STEMI treated by fibrinolysis, coronary flow at 60 min and choice of adjunctive anticoagulant appear to be independent determinants of DeltavWF. Enoxaparin is independently associated with a reduction in DeltavWF and a reduction in death or MI. The clinical benefits of enoxaparin as an adjunctive treatment in STEMI may be mediated in part by a reduction in vWF release.  相似文献   
99.
目的探讨埃兹蛋白(Ezrin)在高分级前列腺上皮内瘤(HGPIN)及前列腺癌(CAP)中的表达及意义。方法采用免疫组化SP法检测44例CaP、12例HGPIN、20例前列腺增生(BPH)及10例正常前列腺(NP)组织中Ezrin的表达。结果31例(70.45%)CaP中Ezrin呈中等或强表达,12例HGPIN中Ezrin均呈弱或中等表达.20例BPH和10例NP中Ezrin没有或星弱表达。在CaP中。Gleason评分(GS)8~10分组的Ezrin表达明显高于7分组和5~6分组(P〈0.05),7分组Ezrin表达明显高于5~6分组(P〈0.05)。结论Ezrin的表达可能与CaP的发生有关,其对诊断HGPIN和判断CaP的转移及预后有重要意义。  相似文献   
100.

Background

The aim of this prospective study was to investigate mitochondrial DNA (mtDNA) copy number in a group of resectable pancreatic cancer (PC) tumor tissues and adjacent normal pancreatic tissues, and to explore the correlation between the mtDNA content in tissues and the clinicopathological parameters and the overall survival.

Methods

Relative mtDNA copy number was measured by the quantitative PCR-based assay. The tumors specimens (n?=?43) originated from the patients with pathologically confirmed pancreatic ductal adenocarcinoma who did not receive any neoadjuvant systemic therapy. The adjacent normal pancreatic tissue samples (n?=?31) were obtained from surgical margins.

Results

mtDNA copy number was significantly lower in PC tissue (P?<?0.001) compared to adjacent normal pancreatic tissue. Jonckheere-Terpstra trend testing indicated a statistically significant decrease in median mtDNA copy number across the differentiation (adjacent normal pancreatic tissue, low-grade, intermediate-grade, high-grade cancer), P?<?0.001. However, the survival analyses failed to show a significant difference in survival between patients with high and low mtDNA copy number.

Conclusions

To the best of our knowledge, we provided the first evidence that mitochondrial DNA copy number was significantly lower in pancreatic cancer tissue (P?<?0.001) compared to adjacent normal pancreatic tissue. Also, we demonstrated that mitochondrial copy number was not a significant marker for predicting prognosis in resectable pancreatic cancer.  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