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   216篇
  免费   14篇
  国内免费   2篇
耳鼻咽喉   1篇
儿科学   12篇
妇产科学   4篇
基础医学   30篇
口腔科学   1篇
临床医学   11篇
内科学   37篇
皮肤病学   3篇
神经病学   6篇
特种医学   58篇
外科学   13篇
综合类   11篇
现状与发展   1篇
预防医学   10篇
眼科学   4篇
药学   13篇
肿瘤学   17篇
  2022年   2篇
  2021年   2篇
  2020年   4篇
  2019年   3篇
  2018年   4篇
  2017年   4篇
  2016年   3篇
  2015年   2篇
  2014年   4篇
  2013年   11篇
  2012年   4篇
  2011年   5篇
  2010年   5篇
  2009年   12篇
  2008年   6篇
  2007年   7篇
  2006年   4篇
  2005年   7篇
  2004年   2篇
  2003年   2篇
  2002年   1篇
  2001年   5篇
  2000年   1篇
  1999年   3篇
  1998年   7篇
  1997年   12篇
  1996年   10篇
  1995年   12篇
  1994年   8篇
  1993年   14篇
  1992年   5篇
  1991年   1篇
  1990年   3篇
  1989年   7篇
  1988年   11篇
  1987年   10篇
  1986年   6篇
  1985年   3篇
  1983年   1篇
  1982年   2篇
  1981年   3篇
  1980年   2篇
  1979年   1篇
  1978年   2篇
  1977年   3篇
  1976年   1篇
  1973年   1篇
  1971年   1篇
  1970年   1篇
  1957年   2篇
排序方式: 共有232条查询结果,搜索用时 15 毫秒
1.
2.
3.
4.
Hereditary hearing impairment affects about 1 in 1000 newborns. In most cases hearing loss is non-syndromic with no other clinical features, while in other families deafness is associated with specific clinical abnormalities. Analysis of large families with non-syndromic and syndromic deafness have been used to identify genes or gene locations that cause hearing impairment. The present report describes a large Norwegian family with autosomal dominant non-syndromic, progressive high tone hearing loss with linkage to 1q21-q23. A maximum LOD score of 7.65 (theta = 0.00) was obtained with the microsatellite marker D1S196. Analysis of recombinant individuals maps the deafness gene (DFNA7) to a 22 cM region between D1S104 and D1S466. The region contains several attractive candidate genes. This report supports the idea of extensive genetic heterogeneity in hereditary hearing impairment and represents the first localization of a deafness gene in a Norwegian family.   相似文献   
5.
Sixteen patients with suspected cerebral metastases were studied with magnetic resonance (MR) imaging before and after the intravenous administration of 0.1 mmol/kg of gadolinium diethylenetriaminepenta-acetic acid. The images were interpreted blindly by two neuroradiologists; all clinical, radiologic (computed tomographic and MR imaging), and pathologic data were reviewed to arrive at a final "best diagnosis," which was then compared with the prior blinded interpretations. Of seven patients found to have multiple metastases, six (86%) had at least one tumor nodule depicted by postinfusion MR imaging that was missed by one or both observers on review of preinfusion images alone. Lesions missed on preinfusion studies were usually small nodules hidden by or not detected next to regions of high-signal edema thought to be related to the adjacent tumor nodule. The authors believe that contrast enhancement improves detection of metastatic foci with MR imaging and that the findings indicate broader implications for the detection of multiple lesions from other causes.  相似文献   
6.
A population based hybrid design combining element of cohort and cross-sectional approach was used to develop a simple clinical algorithm to predict individual probability of developing hypertension (systolic BP > 140 mm Hg and/or diastolic BP > 90 mmHg). 3615 soldiers initially normotensive at the time of induction into high altitude, were studied by systematic random sampling. Multiple logistic regression analysis showed a high significant association between hypertension and age, body mass index (BMI), tobacco smoking and alcohol consumption. Using the constant/coefficient values obtained from the logistic model and the receiver operating characteristics (ROC) curve analysis, the following predictive rule was developed – To the age in years, add (BMIx 3.86); also add 5.53 if he is a smoker; and add 19.81 if he consumes alcohol. If the total exceeds 142, the individual is at high risk of developing hypertension. This algorithm carries a sensitivity of 68.2% and specificity of 78.5%.KEY WORDS: Hypertension, High altitude  相似文献   
7.
8.
A constellation of processes found to be characteristic in the aetiology of elective mutism is explored through clinical material from the psychotherapy of a 5 year‐old girl. The major factors significant in this process are excessive ties to the mother that hinder the child's social–emotional development; difficulties in discharging aggression in a situation when it is not possible to feel separate from mother; primitive ways of dealing with aggressive feelings based on phantasy and omnipotence; and – in my own experience – the symbolic equation of anus and mouth, at the developmental phase of mastery of both speech and sphincter control, as a cause of withholding words.  相似文献   
9.
10.
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