全文获取类型
收费全文 | 2471篇 |
免费 | 440篇 |
国内免费 | 5篇 |
专业分类
耳鼻咽喉 | 40篇 |
儿科学 | 54篇 |
妇产科学 | 36篇 |
基础医学 | 321篇 |
口腔科学 | 69篇 |
临床医学 | 285篇 |
内科学 | 604篇 |
皮肤病学 | 29篇 |
神经病学 | 186篇 |
特种医学 | 95篇 |
外科学 | 429篇 |
综合类 | 272篇 |
一般理论 | 2篇 |
预防医学 | 208篇 |
眼科学 | 40篇 |
药学 | 143篇 |
中国医学 | 2篇 |
肿瘤学 | 101篇 |
出版年
2021年 | 51篇 |
2020年 | 23篇 |
2019年 | 35篇 |
2018年 | 45篇 |
2017年 | 33篇 |
2016年 | 31篇 |
2015年 | 30篇 |
2014年 | 46篇 |
2013年 | 74篇 |
2012年 | 125篇 |
2011年 | 118篇 |
2010年 | 60篇 |
2009年 | 57篇 |
2008年 | 101篇 |
2007年 | 114篇 |
2006年 | 98篇 |
2005年 | 106篇 |
2004年 | 110篇 |
2003年 | 87篇 |
2002年 | 115篇 |
2001年 | 112篇 |
2000年 | 116篇 |
1999年 | 100篇 |
1998年 | 32篇 |
1997年 | 26篇 |
1996年 | 37篇 |
1995年 | 19篇 |
1994年 | 25篇 |
1993年 | 18篇 |
1992年 | 67篇 |
1991年 | 67篇 |
1990年 | 55篇 |
1989年 | 52篇 |
1988年 | 62篇 |
1987年 | 62篇 |
1986年 | 66篇 |
1985年 | 59篇 |
1984年 | 43篇 |
1983年 | 42篇 |
1982年 | 24篇 |
1981年 | 25篇 |
1980年 | 33篇 |
1979年 | 31篇 |
1978年 | 23篇 |
1975年 | 16篇 |
1973年 | 22篇 |
1972年 | 22篇 |
1969年 | 21篇 |
1968年 | 17篇 |
1967年 | 20篇 |
排序方式: 共有2916条查询结果,搜索用时 15 毫秒
61.
Increased concanavalin A induced suppression in treated and untreated coeliac disease. 总被引:2,自引:0,他引:2 下载免费PDF全文
The generation of suppression by concanavalin A in peripheral blood mononuclear cells in treated and untreated coeliac subjects using an in vitro assay was found to be significantly increased when compared with controls. The response of peripheral blood mononuclear cells to the plant mitogen concanavalin A (con A) was also significantly depressed in both groups of coeliac patients. It is proposed that the depressed cell mediated immunity found in this and other studies in coeliac patients is because of increased suppression. The possible connection between these findings and the increased incidence of malignancy also found in coeliac disease is discussed. 相似文献
62.
63.
Xin Sheng Chengxiang Qiu Hongbo Liu Caroline Gluck Jesse Y. Hsu Jiang He Chi-yuan Hsu Daohang Sha Matthew R. Weir Tamara Isakova Dominic Raj Hernan Rincon-Choles Harold I. Feldman Raymond Townsend Hongzhe Li Katalin Susztak 《Proceedings of the National Academy of Sciences of the United States of America》2020,117(46):29013
64.
65.
Magdy Giurgius Nicole Fearing Alexandra Weir Lada Micheas Archana Ramaswamy 《Surgical endoscopy》2014,28(5):1454-1459
Background
Endoscopic sclerotherapy using sodium morrhuate has been used to treat patients with weight regain after Roux-en-Y gastric bypass whose presumed etiology is loss of restriction due to gastrojejunostomy dilation. Weight loss and stability have been demonstrated in several studies with short-term follow-up evaluation.Methods
This retrospective review evaluated all the patients who underwent sclerotherapy for a dilated gastrojejunostomy between 2007 and 2012.Results
The study identified 48 patients with a mean follow-up period of 22 months (range 12–60 months). The mean age of these patients was 47.5 ± 10.5 years, and 92 % were women. The average weight loss from the primary procedure was 132.5 ± 54.82 lb, and the average weight regain from the lowest weight to the maximum weight before sclerotherapy was 46 ± 40.32 lb. The median number of sclerotherapy sessions was two (range 1–4). The pre-procedure mean gastrojejunostomy diameter was 20 ± 3.6 mm, and the mean volume of sodium morrhuate injected per session was 12.8 ± 3.7 ml. The average weight loss from sclerotherapy to the final documented weight was 3.17 ± 19.70 lb, which was not statistically significant. The following variables in the multivariate analysis were not associated with statistically significant weight loss: volume of sodium morrhuate, patient age, gastrojejunostomy diameter, number of sclerotherapy sessions, decrease in gastrojejunostomy diameter between the first and second sessions, and number of follow-up years. Weight stabilization or loss was achieved by 58 % of our cohort, with a mean weight loss of 15.9 ± 14.6 lb in this subgroup.Conclusion
The long-term follow-up evaluation of patients undergoing sclerotherapy of the gastrojejunostomy for weight regain after gastric bypass showed only a marginal weight loss, which was not statistically significant in our study population, although more than 50 % of the patients achieved weight loss or stabilization. 相似文献66.
S. R. Majumdar F. A. McAlister J. A. Johnson D. L. Weir D. Bellerose D. A. Hanley A. S. Russell B. H. Rowe 《Osteoporosis international》2014,25(9):2173-2179
Summary
Most patients are not treated for osteoporosis after their fragility fracture “teachable moment.” Among almost 400 consecutive wrist fracture patients, we determined that better-than-average osteoporosis knowledge (adjusted odds?=?2.6) and BMD testing (adjusted odds?=?6.5) were significant modifiable facilitators of bisphosphonate treatment while male sex, working outside the home, and depression were major barriers.Introduction
In the year following fragility fracture, fewer than one quarter of patients are treated for osteoporosis. Although much is known regarding health system and provider barriers and facilitators to osteoporosis treatment, much less is understood about modifiable patient-related factors.Methods
Older patients with wrist fracture not treated for osteoporosis were enrolled in trials that compared a multifaceted intervention with usual care controls. Baseline data included a test of patient osteoporosis knowledge. We then determined baseline factors that independently predicted starting bisphosphonate treatment within 1 year.Results
Three hundred seventy-four patients were enrolled; mean age 64 years, 78 % women, 90 % white, and 54 % with prior fracture. Within 1 year, 86 of 374 (23 %) patients were treated with bisphosphonates. Patients who were treated had better osteoporosis knowledge at baseline (70 % correct vs 57 % for untreated, p?0.001) than patients who remained untreated; conversely, untreated patients were more likely to be male, still working, and report depression. In fully adjusted models, osteoporosis knowledge was independently associated with starting bisphosphonates (adjusted OR 2.6, 95 %CI 1.3–5.3). Obtaining a BMD test (aOR 6.5, 95 %CI 3.4–12.2) and abnormal BMD results (aOR 34.5, 95 %CI 16.8–70.9) were strongly associated with starting treatment.Conclusions
The most important modifiable facilitators of osteoporosis treatment in patients with fracture were knowledge and BMD testing. Specifically targeting these two patient-level factors should improve post-fracture treatment rates. 相似文献67.
Niranjan Rao Vijay O. Bhargava Donald L. Reynolds Mark G. Eller Scott J. Weir 《Biopharmaceutics & drug disposition》1996,17(9):753-760
The dose proportionality of deflazacort was assessed following single-dose oral administration at doses of 3, 6, and 36 mg to 24 healthy young adult volunteers. The active metabolite of deflazacort (21-desacetyl deflazacort) was monitored in plasma using a sensitive, semi-microbore liquid chromatographic method. Cmax averaged 10·4±5·0, 19·8±7·5, and 132·6±52·5 ng mL−1 for the 3, 6, and 36 mg doses, respectively. AUC(0–∞) averaged 38·5±37·1, 64·9±20·8, and 411·7±148·5 ng h mL−1 for the same three doses, respectively. Elimination half-life ranged from 1·9±0·5 h at the 6 mg dose to 2·4±1·5 h at the 36 mg dose. Regression analyses of dose versus Cmax and AUC(0–∞) yielded intercepts which were not significantly different from zero (p>0·05) and slopes which were significant (p<0·05). Regression analysis of dose versus apparent oral clearance yielded a slope which was not significantly different from zero (p>0·05). These data indicate that deflazacort exhibits dose-proportional pharmacokinetics. 相似文献
68.
Sean T. Allen Suzanne M. Grieb Jennifer L. Glick Rebecca Hamilton White Tyler Puryear Katherine C. Smith Brian W. Weir Susan G. Sherman 《Annals of medicine》2022,54(1):404
IntroductionDespite decades of empirical research in the US and internationally documenting the benefits of implementing syringe services programs (SSPs), their implementation may be controversial in many jurisdictions. Better understanding how research evidence is applied during SSP implementation processes may enable the public health workforce to advocate for program scale up. This study explores applications of research evidence during processes to acquire approvals for SSP implementation in rural counties in Kentucky.MethodsIn-depth interviews were conducted among eighteen stakeholders (e.g. health department directors, SSP operators) involved in SSP implementation in rural Kentucky counties. Stakeholders were asked to describe the contexts surrounding SSP implementation processes. Interviews were transcribed and analysed for applications of research evidence. Research evidence-related quotes were subsequently categorised based on the typologies for applications of research evidence developed by Weiss et al. (instrumental, conceptual, and symbolic) and a fourth category for instances when research evidence was not used.ResultsInstrumental applications of research evidence occurred at the intrapersonal and interpersonal levels to dispel concerns about SSPs and formed the basis for implementation support. SSP proponents used research evidence in a conceptual manner to address underlying attitudes and beliefs that were not evidence-based. Participants reported symbolic research evidence applications to justify pre-existing attitudes and beliefs about meeting the public health needs of people who inject drugs. Lastly, in some instances, research evidence was met with scepticism and an unwillingness to consider its merits.ConclusionApplications of research evidence during SSP implementation approval processes in rural Kentucky counties were heterogeneous in nature. Better understanding the diversity of ways in which research evidence may be employed during SSP implementation processes may support efforts to improve the public health of people who inject drugs.
Key messages
- Applications of research evidence during SSP implementation approval processes in rural Kentucky counties were heterogeneous in nature.
- Instrumental applications of research evidence occurred at the intrapersonal and interpersonal levels to dispel concerns about SSPs and formed the basis for implementation support.
- SSP proponents used research evidence in a conceptual manner to address underlying attitudes and beliefs that were not evidence-based.
69.
Emily Wang Yeyi Zhu Rana F. Chehab Jing Wu Stefanie N. Hinkle Natalie L. Weir Andrew A. Bremer Jiaxi Yang Zhen Chen Michael Y. Tsai Cuilin Zhang 《Nutrients》2022,14(3)
Despite increasing interest in the health effects of polyunsaturated FAs (PUFAs), their roles in fetal and neonatal growth remain understudied. Within the NICHD Fetal Growth Studies—Singleton Cohort, we prospectively investigated the associations of individual and subclasses of plasma phospholipid PUFAs at gestational weeks (GW) 10–14, 15–26, 23–31, and 33–39 with neonatal anthropometric measures as surrogates for fetal growth among 107 women with gestational diabetes mellitus (GDM) and 214 non-GDM controls. Multivariable weighted linear regression models estimated the associations between plasma phospholipid PUFAs and neonatal anthropometric measures. Adjusted beta coefficients for phospholipid docosahexaenoic acid (DHA) per standard deviation (SD) increase at GW 23–31 in association with birthweight z-score, neonatal length, and neonatal fat mass were 0.25 (95% CI: 0.08–0.41), 0.57 (0.11–1.03) cm, and 54.99 (23.57–86.42) g, respectively; all false discovery rates (FDRs) < 0.05. Estimated Δ5-desaturase activity per SD increase at GW 33–39 but not at other time points was positively associated with birthweight z-score: 0.29 (95% CI: 0.08–0.33); neonatal length: 0.61 (0.29–0.94) cm; and neonatal fat mass: 32.59 (8.21–56.96) g; all FDRs < 0.05. Longitudinal analysis showed consistent results. Our findings suggest that mid-to-late pregnancy presented as critical windows for primarily diet-derived DHA and Δ5-desaturase activity in relation to neonatal anthropometric measures. 相似文献
70.