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   9010篇
  免费   589篇
  国内免费   31篇
耳鼻咽喉   127篇
儿科学   359篇
妇产科学   231篇
基础医学   1182篇
口腔科学   346篇
临床医学   612篇
内科学   2197篇
皮肤病学   245篇
神经病学   722篇
特种医学   394篇
外科学   1314篇
综合类   31篇
一般理论   2篇
预防医学   732篇
眼科学   180篇
药学   436篇
中国医学   44篇
肿瘤学   476篇
  2023年   54篇
  2022年   48篇
  2021年   315篇
  2020年   188篇
  2019年   299篇
  2018年   356篇
  2017年   223篇
  2016年   204篇
  2015年   272篇
  2014年   339篇
  2013年   440篇
  2012年   672篇
  2011年   682篇
  2010年   399篇
  2009年   331篇
  2008年   517篇
  2007年   514篇
  2006年   494篇
  2005年   442篇
  2004年   416篇
  2003年   397篇
  2002年   363篇
  2001年   223篇
  2000年   213篇
  1999年   211篇
  1998年   53篇
  1997年   62篇
  1996年   42篇
  1995年   45篇
  1994年   27篇
  1993年   33篇
  1992年   70篇
  1991年   69篇
  1990年   75篇
  1989年   60篇
  1988年   55篇
  1987年   65篇
  1986年   44篇
  1985年   37篇
  1984年   25篇
  1983年   25篇
  1982年   13篇
  1981年   13篇
  1979年   31篇
  1977年   16篇
  1976年   18篇
  1974年   13篇
  1973年   12篇
  1972年   13篇
  1967年   13篇
排序方式: 共有9630条查询结果,搜索用时 31 毫秒
1.
The innate immune response generated against influenza infection is critical for the inhibition of viral dissemination. The trachea contains different types of innate immune cells that protect the respiratory tract from pathogen invasion. Among them, γδ T cells have the ability to rapidly generate large amounts of pro-inflammatory cytokines to preserve mucosal barrier homeostasis during infection. However, little is known about their role during the early phase of influenza infection in the airways. In this study, we found that, early after infection, γδ T cells are recruited and activated in the trachea and outnumber αβ T cells during the course of the influenza infection that follows. We also showed that the majority of the recruited γδ T cells express the Vγ4 TCR chain and infiltrate in a process that involves the chemokine receptor CXCR3. In addition, we demonstrated that γδ T cells promote the recruitment of protective neutrophils and NK cells to the tracheal mucosa. Altogether, our results highlight the importance of the immune responses mediated by γδ T cells.  相似文献   
2.
3.
4.
5.
6.
7.
8.
The CAV-AEP annually publishes the immunisation schedule considered optimal for all children and adolescent resident in Spain, taking into account the available evidence.The 2 + 1 schedule is recommended (2, 4, and 11 months) with hexavalent vaccines (DTPa-VPI-Hib-HB) and with 13-valent pneumococcal conjugate.A 6-year booster is recommended, preferably with DTPa (if available), with a dose of polio for those who received 2 + 1 schemes, as well as vaccination with Tdpa in adolescents and in each pregnancy, preferably between 27 and 32 weeks.Rotavirus vaccine should be systematic for all infants.Meningococcal B vaccine, with a 2 + 1 schedule, should be included in routine calendar.In addition to the inclusion of the conjugated tetravalent meningococcal vaccine (MenACWY) at 12 years of age with catch up to 18 years, inclusive, the CAV recommends this vaccine to be also included at 12 months of age, replacing MenC. Likewise, it is recommended in those over 6 weeks of age with risk factors or who travel to countries with a high incidence of these serogroups.Two-dose schedules for triple viral (12 months and 3-4 years) and varicella (15 months and 3-4 years) will be used. The second dose could be applied as a tetraviral vaccine.Universal systematic vaccination against HPV is recommended, regardless of gender, preferably at 12 years, and greater effort should be made to improve coverage. The 9 genotype extends coverage for both genders.  相似文献   
9.
10.
Fibrous dysplasia is a non‐neoplastic developmental process that affects the craniofacial bones, characterized by painless enlargement as a result of bone substitution by abnormal fibrous tissue. Postzygotic somatic activating mutations in the GNAS1 gene cause fibrous dysplasia and have been extensively investigated, as well as being helpful in the differential diagnosis of the disease. Fibrous dysplasia may involve one (monostotic) or multiple bones (polyostotic), sporadically or in association with McCune‐Albright syndrome, Jeffe‐Lichenstein syndrome, or Mazabreud syndrome. This review summarizes the current knowledge on fibrous dysplasia, emphasizing the value of integrating the understanding of its molecular pathogenesis with the clinical, radiological, and histopathological features. In addition, we address important aspects related to the differential diagnosis and patient management.  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