首页 | 官方网站   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   32091篇
  免费   2513篇
  国内免费   73篇
医药卫生   34677篇
  2023年   170篇
  2022年   112篇
  2021年   500篇
  2020年   446篇
  2019年   749篇
  2018年   781篇
  2017年   588篇
  2016年   711篇
  2015年   791篇
  2014年   973篇
  2013年   1562篇
  2012年   2110篇
  2011年   2158篇
  2010年   1194篇
  2009年   1102篇
  2008年   2029篇
  2007年   2183篇
  2006年   2155篇
  2005年   2085篇
  2004年   1965篇
  2003年   1885篇
  2002年   1769篇
  2001年   386篇
  2000年   337篇
  1999年   378篇
  1998年   465篇
  1997年   326篇
  1996年   291篇
  1995年   297篇
  1994年   255篇
  1993年   257篇
  1992年   225篇
  1991年   220篇
  1990年   216篇
  1989年   206篇
  1988年   196篇
  1987年   186篇
  1986年   180篇
  1985年   204篇
  1984年   174篇
  1983年   173篇
  1982年   185篇
  1981年   166篇
  1980年   168篇
  1979年   109篇
  1978年   111篇
  1977年   100篇
  1976年   102篇
  1975年   95篇
  1974年   101篇
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
81.
82.
One hundred forty five individuals who sought medical attention as a result of a motor vehicle accident (MVA), and who were initially assessed 1 to 4 months post-MVA, were followed up prospectively for 6 months to determine how many of the 55 with posttraumatic stress disorder (PTSD) and the 43 with sub-syndromal PTSD would remit and what variables would predict remission. Thirty (55%) of those with initial PTSD had remitted at least in part by 6 months while 67% of those with sub-syndromal PTSD had remitted (and 5% had worsened). Four variables, including severity of initial symptoms, degree of initial physical injury, relative degree of physical recovery by 4 months and whether a close family member suffered a trauma during the follow-up interval, combined to classify 6-month clinical status of 84% of those with initial PTSD secondary to MVAs.  相似文献   
83.
84.
85.
86.
87.
88.
Summary: Strategies used in molecular genetics have changed modern neurology. The gene or genes responsible for several major neurologic diseases have now been identified using "reverse" or positional genetics. Unexpected new genetic mechanisms have been discovered in human neurologic diseases, including (a) identical mutations of the prion protein gene in Creutzfeldt-Jakob disease and fatal familial insomnia with the phenotypic expression directed by an accompanying polymorphism; (b) stable duplications of chromosome 17 in Charcot-Marie-Tooth disease (type 1 A) that involve many genes, only one of which appears to cause neuropathy; and (c) highly variable, dynamic mutations in myotonic dystrophy, fragile X syndrome, and Kennedy's syndrome that modulate variable expressivity in multiple tissues. There is growing recognition that neurologic diseases are often complex genetic diseases with multifactorial rather than simple modes of inheritance. For example, genetic association/linkage strategies have interacted with biochemistry and immunopathology studies to produce new insights into the disease mechanism of late-onset Alzheimer's disease. The role of apolipoprotein E in late-onset Alzheimer's disease is an example of how new analytical techniques of genetic disease can be applied to dissect multiple genes. Similar research strategies are suggested for the study of epilepsy as a complex disease.  相似文献   
89.
Alexithymia was measured in non-treatment seeking, community-dwelling Holocaust survivors using the Toronto Alexithymia Scale—Twenty Item Version (TAS-20). Scores of survivors with (n = 30) and without (n = 26) posttraumatic stress disorder (PTSD) were compared, and associations among alexithymia, severity of trauma, and severity of PTSD symptoms were determined. Survivors with PTSD had significantly higher scores on the TAS-20 compared to survivors without PTSD. TAS-20 scores were significantly associated with severity of PTSD symptoms, but not with severity of trauma. This study adds to our knowledge of the relationship between alexithymia and trauma by demonstrating that this characteristic is related to the presence of posttraumatic symptoms and not simply exposure to trauma.  相似文献   
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-23

京公网安备 11010802026262号