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   423篇
  免费   37篇
  2021年   6篇
  2020年   4篇
  2019年   3篇
  2017年   6篇
  2016年   8篇
  2015年   14篇
  2014年   19篇
  2013年   15篇
  2012年   18篇
  2011年   23篇
  2010年   19篇
  2009年   17篇
  2008年   21篇
  2007年   16篇
  2006年   12篇
  2005年   14篇
  2004年   19篇
  2003年   13篇
  2002年   17篇
  2001年   13篇
  2000年   17篇
  1999年   13篇
  1998年   10篇
  1997年   4篇
  1996年   8篇
  1995年   5篇
  1994年   7篇
  1993年   6篇
  1992年   6篇
  1991年   9篇
  1990年   5篇
  1989年   10篇
  1988年   3篇
  1987年   3篇
  1986年   6篇
  1984年   3篇
  1981年   3篇
  1979年   2篇
  1978年   6篇
  1977年   3篇
  1976年   4篇
  1975年   4篇
  1972年   2篇
  1971年   2篇
  1968年   8篇
  1967年   4篇
  1966年   3篇
  1965年   3篇
  1963年   2篇
  1959年   2篇
排序方式: 共有460条查询结果,搜索用时 31 毫秒
81.
82.

Background  

Over 50% of patients with upper limb paresis resulting from stroke face long-term impaired arm function and ensuing disability in daily life. Unfortunately, the number of effective treatments aimed at improving arm function due to stroke is still low. This study aims to evaluate a new therapy for improving arm function in sub-acute stroke patients based on mental practice theories and functional task-oriented training, and to study the predictors for a positive treatment result. It is hypothesized that a six-week, mental practice-based training program (additional to regular therapy) targeting the specific upper extremity skills important to the individual patient will significantly improve both arm function and daily activity performance, as well as being cost effective.  相似文献   
83.

Background  

The aim of this study was to evaluate long-term platinum retention in patients treated with cisplatin and oxaliplatin.  相似文献   
84.
85.
86.

Background  

The influenza A virus is an important infectious cause of morbidity and mortality in humans and was responsible for 3 pandemics in the 20th century. As the replication of the influenza virus is based on its host's machinery, codon usage of its viral genes might be subject to host selection pressures, especially after interspecies transmission. A better understanding of viral evolution and host adaptive responses might help control this disease.  相似文献   
87.
The declaration of the human influenza A pandemic (H1N1) 2009 (H1N1/09) raised important questions, including origin and host range [1], [2]. Two of the three pandemics in the last century resulted in the spread of virus to pigs (H1N1, 1918; H3N2, 1968) with subsequent independent establishment and evolution within swine worldwide [3]. A key public and veterinary health consideration in the context of the evolving pandemic is whether the H1N1/09 virus could become established in pig populations [4]. We performed an infection and transmission study in pigs with A/California/07/09. In combination, clinical, pathological, modified influenza A matrix gene real time RT-PCR and viral genomic analyses have shown that infection results in the induction of clinical signs, viral pathogenesis restricted to the respiratory tract, infection dynamics consistent with endemic strains of influenza A in pigs, virus transmissibility between pigs and virus-host adaptation events. Our results demonstrate that extant H1N1/09 is fully capable of becoming established in global pig populations. We also show the roles of viral receptor specificity in both transmission and tissue tropism. Remarkably, following direct inoculation of pigs with virus quasispecies differing by amino acid substitutions in the haemagglutinin receptor-binding site, only virus with aspartic acid at position 225 (225D) was detected in nasal secretions of contact infected pigs. In contrast, in lower respiratory tract samples from directly inoculated pigs, with clearly demonstrable pulmonary pathology, there was apparent selection of a virus variant with glycine (225G). These findings provide potential clues to the existence and biological significance of viral receptor-binding variants with 225D and 225G during the 1918 pandemic [5].  相似文献   
88.
89.
90.
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