全文获取类型
收费全文 | 1490篇 |
免费 | 114篇 |
国内免费 | 8篇 |
专业分类
耳鼻咽喉 | 7篇 |
儿科学 | 68篇 |
妇产科学 | 13篇 |
基础医学 | 155篇 |
口腔科学 | 87篇 |
临床医学 | 209篇 |
内科学 | 340篇 |
皮肤病学 | 26篇 |
神经病学 | 71篇 |
特种医学 | 268篇 |
外科学 | 107篇 |
综合类 | 28篇 |
预防医学 | 66篇 |
眼科学 | 24篇 |
药学 | 86篇 |
中国医学 | 6篇 |
肿瘤学 | 51篇 |
出版年
2023年 | 10篇 |
2021年 | 21篇 |
2020年 | 12篇 |
2019年 | 11篇 |
2018年 | 32篇 |
2017年 | 15篇 |
2016年 | 21篇 |
2015年 | 25篇 |
2014年 | 37篇 |
2013年 | 36篇 |
2012年 | 43篇 |
2011年 | 38篇 |
2010年 | 55篇 |
2009年 | 65篇 |
2008年 | 43篇 |
2007年 | 36篇 |
2006年 | 31篇 |
2005年 | 33篇 |
2004年 | 24篇 |
2003年 | 28篇 |
2002年 | 31篇 |
2001年 | 27篇 |
2000年 | 23篇 |
1999年 | 29篇 |
1998年 | 52篇 |
1997年 | 59篇 |
1996年 | 67篇 |
1995年 | 52篇 |
1994年 | 45篇 |
1993年 | 52篇 |
1992年 | 29篇 |
1991年 | 21篇 |
1990年 | 31篇 |
1989年 | 62篇 |
1988年 | 57篇 |
1987年 | 52篇 |
1986年 | 45篇 |
1985年 | 36篇 |
1984年 | 27篇 |
1983年 | 13篇 |
1982年 | 26篇 |
1981年 | 18篇 |
1980年 | 10篇 |
1979年 | 8篇 |
1978年 | 11篇 |
1977年 | 20篇 |
1976年 | 21篇 |
1975年 | 15篇 |
1974年 | 8篇 |
1973年 | 9篇 |
排序方式: 共有1612条查询结果,搜索用时 234 毫秒
1.
ME BURGE AM JOSHUA CM McNEIL R HUI MJ BOYER R ABRAHAM 《Asia-Pacific Journal of Clinical Oncology》2005,1(1):47-52
Background: Pemetrexed and cisplatin have recently been shown to significantly improve survival compared with cisplatin alone. However, there are only limited data reflecting teaching hospital experience outside a clinical trial. Pemetrexed has only been available in Australia on a restricted basis since 2002. We reviewed our experience of patients treated on the Australian ‘Special Access Scheme’ at three major thoracic oncology units. Methods: Charts were reviewed for all patients enrolled on the scheme. Data was extracted on age, World Health Organization (WHO) performance status, histology, prior therapy, time from diagnosis to starting pemetrexed, chemotherapy (pemetrexed alone or with a platinum), cycle number, response rate, actuarial progression‐free and overall survival. Doses were cisplatin 75 mg/m2 or carboplatin AUC = 5 and pemetrexed 500 mg/m2 every 21 days. Results: 52 patients (32 male and 20 female) were reviewed. Median age was 58 years and 88% were WHO 0–1. Histology included 54% epithelial, 17% biphasic (epithelial and sarcomatoid) and 21% undefined. The median time from diagnosis to administration of pemetrexed was 145 days. Sixty‐five percent had minimal surgical intervention with video assisted thoracoscopy, pleurodesis and biopsy, while 19% had received prior palliative radiation. Seventy‐one percent were chemotherapy naïve, the remaining 29% having received previous platinum and/or gemcitabine regimens. Twenty‐three percent had pemetrexed alone, 35% in combination with carboplatin and 42% with cisplatin. The median number of cycles was 4 (range 1–13). The response rate was 33%. No toxicity was observed in 20% grade 3–4 toxicity in 10% (majority nausea/vomiting). The median progression‐free and overall survival times from starting pemetrexed were 184 days and 298 days, respectively. Conclusions: Pemetrexed‐based regimens are safe and effective in a community setting in malignant mesothelioma. 相似文献
2.
The effect of elevated glucose levels on myo-inositol metabolism in cultured bovine aortic endothelial cells 总被引:3,自引:0,他引:3
Bovine aorta endothelial cells were used to determine the effect of high ambient glucose concentrations on myo-inositol metabolism. Culturing the cells for a minimum of 1 week in elevated glucose concentrations caused an increase in the intracellular sorbitol content and a decrease in myo-inositol levels. The accumulation of myo-inositol from the medium and incorporation into phospholipids was reduced 25% to 50% in cells grown in the presence of 30 to 50 mmol/L glucose. This effect was not observed following a short-term exposure of the cells to elevated glucose levels. Kinetic analysis of high-affinity myo-inositol uptake showed that the K'm was significantly increased in cells grown in 30 mmol/L glucose compared to those cultured in 5.6 mmol/L glucose. This would suggest that exposing endothelial cells to high ambient glucose levels for a minimum of 1 week leads to a competitive type of inhibition of high-affinity myo-inositol uptake. The changes in myo-inositol metabolism and content and sorbitol levels mediated by glucose exposure were blocked by addition of the aldose reductase inhibitor, sorbinil, to the media, suggesting that these changes are caused by the accumulation of sorbitol by the cells. Exposure of bovine aorta endothelial cells to high ambient levels of glucose leads to accumulation of sorbitol in the cells, which is responsible for alterations in myo-inositol metabolism. These changes could result in alteration of endothelial cell membrane function and contribute to the pathology of diabetes mellitus. 相似文献
3.
A brief review of the developmental background of the lateral cervical sinuses, fistulas, cysts and auricles has been presented. In all likelihood they are of branchial cleft origin. Surgical excision is the recommended treatment as shown in the cases described. 相似文献
4.
5.
6.
7.
8.
9.
10.
Robert L. Koegel Laura Schreibman Lauren M. Loos Hanne Dirlich-Wilhelm Glen Dunlap Frank R. Robbins Anthony J. Plienis 《Journal of autism and developmental disorders》1992,22(2):205-216
The present study extends the area of research on stress in parents of autistic children. In this study we used the Questionnaire on Resources and Stress (Holroyd, 1987) to compare the stress profiles across mothers (a) who lived in different cultural and geographic environments; (b) who had children of different ages; and (c) who had children with different functioning levels. Results showed a characteristic profile that was highly consistent across each of these subgroups. Major differences from the normative data occurred on scales measuring stress associated with dependency and management, cognitive impairment, limits on family opportunity, and life-span care. Results suggest the importance of developing treatment programs aimed at reducing stress in specific areas in families with autistic children.Orchard Mental Health CenterThis research was supported by U.S. Department of Education, NIDRR Cooperative Agreement No. G0087C0234 (Koegel and Dunlap), by U.S. Public Health Service Research Grants MH28210 (Koegel) and MH39434 (Schreibman) from the National Institute of Mental Health, by Grant No. G008530082 from the U.S. Department of Education, Handicapped Children's Early Education Program (Dunlap), and by Fogarty Senior International Fellowship 1 FOB TWO 1374-01 (Schreibman) from the Fogarty International Center of the National Institutes of Health. The authors acknowledge the contributions of Prof. Dr. med. Hedwig Amorosa, and Dorle Staniczek, Soz. Pad. of the Max Planck Institute for Psychiatry, Munich, West Germany, and express particular appreciation to Prof. Dr. med. D. Ploog, Director of the Institute. 相似文献