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   1181135篇
  免费   318909篇
  国内免费   43117篇
耳鼻咽喉   16100篇
儿科学   29810篇
妇产科学   29075篇
基础医学   210593篇
口腔科学   29255篇
临床医学   140481篇
内科学   258744篇
皮肤病学   21862篇
神经病学   94741篇
特种医学   46460篇
外国民族医学   213篇
外科学   182300篇
综合类   87789篇
现状与发展   25篇
一般理论   284篇
预防医学   108761篇
眼科学   40053篇
药学   128531篇
  59篇
中国医学   52294篇
肿瘤学   65731篇
  2019年   21187篇
  2018年   24074篇
  2017年   22642篇
  2016年   21889篇
  2015年   24347篇
  2014年   28507篇
  2013年   33621篇
  2012年   41710篇
  2011年   44907篇
  2010年   34494篇
  2009年   39764篇
  2008年   38690篇
  2007年   37770篇
  2006年   37048篇
  2005年   36901篇
  2004年   36703篇
  2003年   34621篇
  2002年   33480篇
  2001年   48179篇
  2000年   44971篇
  1999年   44214篇
  1998年   22848篇
  1997年   21796篇
  1996年   22252篇
  1995年   21875篇
  1994年   21185篇
  1993年   19289篇
  1992年   38318篇
  1991年   37046篇
  1990年   35564篇
  1989年   34420篇
  1988年   32597篇
  1987年   31613篇
  1986年   29976篇
  1985年   28382篇
  1984年   21989篇
  1983年   19598篇
  1982年   15270篇
  1981年   14187篇
  1980年   13378篇
  1979年   22331篇
  1978年   16968篇
  1977年   15285篇
  1976年   14125篇
  1975年   14685篇
  1974年   16936篇
  1973年   16173篇
  1972年   15528篇
  1971年   14152篇
  1970年   13464篇
排序方式: 共有10000条查询结果,搜索用时 359 毫秒
101.
骨碎补是历代临床常用中药,具有疗伤止痛、补肾强骨、消风祛斑等功效。其主要含黄酮、苯丙素、三萜、酚酸及其苷等类化学成分,现代研究表明骨碎补具有抗骨质疏松、促进骨折愈合、促软骨再生、护牙健齿、保护肾功能、抗炎、防治中毒性耳聋、降血脂等多种生物活性,开发前景广阔。本文对近年来骨碎补的化学成分、药理作用及临床应用研究进行综述,以期为骨碎补的进一步深入系统的研究和开发利用提供依据。  相似文献   
102.
103.
104.
105.
106.
107.
108.
109.
PurposeOur purpose was to determine the effect of chemoradiotherapy (CRT) on patient-reported quality of life (QOL) for patients with intact pancreas cancer.Methods and MaterialsWe reviewed a prospective QOL registry for patients with intact, clinically localized pancreatic ductal adenocarcinoma treated with CRT between June 2015 and November 2018. QOL was assessed pre-CRT (immediately before CRT, after neoadjuvant chemotherapy) and at the completion of CRT with the Functional Assessment of Cancer Therapy-Hepatobiliary (FACT-Hep) and its component parts: FACT-General (FACT-G) and hepatobiliary cancer subscore (HCS). A minimally important difference from pre-CRT was defined as ≥ 6, 5, and 8 points for FACT-G, HCS, and FACT-Hep, respectively.ResultsOf 157 patients who underwent CRT, 100 completed both pre- and post-CRT surveys and were included in the primary analysis. Median age at diagnosis was 65 years (range, 23-90). National Comprehensive Cancer Network resectability status was resectable (3%), borderline resectable (40%), or locally advanced (57%). Folinic acid, 5-fluorouracil, irinotecan, and oxaliplatin (FOLFIRINOX) (75%) or gemcitabine and nab-paclitaxel (42%) were given for a median of 6 cycles (range, 0-42) before CRT. Radiation therapy techniques included 3-dimensional conformal (22%), intensity modulated photon (55%), and intensity modulated proton (23%) radiation therapy to a median dose of 50 Gy (range, 36-62.5). Concurrent chemotherapy was most commonly capecitabine (82%). Sixty-three patients (63%) had surgery after CRT. The mean decline in FACT-G, HCS subscale, and FACT-Hep from pre- to post-CRT was 3.5 (standard deviation [SD], 13.7), 1.7 (SD 7.8), and 5.2 (SD 19.4), respectively. Each of these changes were statistically significant, but did not meet the minimally important difference threshold. Pancreatic head tumor location was associated with decline in FACT-Hep. Nausea was the toxicity with the greatest increase from pre- to post-CRT by both physician-assessment and patient-reported QOL.ConclusionsFor patients with intact pancreatic adenocarcinoma, modern CRT is well tolerated with minimal decline in QOL during treatment.  相似文献   
110.
The retroviral protease of human immunodeficiency virus (HIV) is an excellent target for antiviral inhibitors for treating HIV/AIDS. Despite the efficacy of therapy, current efforts to control the disease are undermined by the growing threat posed by drug resistance. This review covers the historical background of studies on the structure and function of HIV protease, the subsequent development of antiviral inhibitors, and recent studies on drug-resistant protease variants. We highlight the important contributions of Dr. Stephen Oroszlan to fundamental knowledge about the function of the HIV protease and other retroviral proteases. These studies, along with those of his colleagues, laid the foundations for the design of clinical inhibitors of HIV protease. The drug-resistant protease variants also provide an excellent model for investigating the molecular mechanisms and evolution of resistance.  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