全文获取类型
收费全文 | 218728篇 |
免费 | 13484篇 |
国内免费 | 2006篇 |
专业分类
耳鼻咽喉 | 2705篇 |
儿科学 | 5474篇 |
妇产科学 | 5894篇 |
基础医学 | 30752篇 |
口腔科学 | 5370篇 |
临床医学 | 19887篇 |
内科学 | 41741篇 |
皮肤病学 | 3773篇 |
神经病学 | 18034篇 |
特种医学 | 7905篇 |
外国民族医学 | 6篇 |
外科学 | 33024篇 |
综合类 | 6295篇 |
一般理论 | 166篇 |
预防医学 | 16886篇 |
眼科学 | 4896篇 |
药学 | 16674篇 |
中国医学 | 924篇 |
肿瘤学 | 13812篇 |
出版年
2022年 | 1420篇 |
2021年 | 3049篇 |
2020年 | 1898篇 |
2019年 | 3129篇 |
2018年 | 4154篇 |
2017年 | 2987篇 |
2016年 | 3178篇 |
2015年 | 3713篇 |
2014年 | 5313篇 |
2013年 | 7145篇 |
2012年 | 11055篇 |
2011年 | 11737篇 |
2010年 | 6846篇 |
2009年 | 6165篇 |
2008年 | 10479篇 |
2007年 | 11047篇 |
2006年 | 10756篇 |
2005年 | 10038篇 |
2004年 | 9672篇 |
2003年 | 8787篇 |
2002年 | 8330篇 |
2001年 | 7576篇 |
2000年 | 7482篇 |
1999年 | 6587篇 |
1998年 | 3051篇 |
1997年 | 2297篇 |
1996年 | 1684篇 |
1995年 | 1542篇 |
1994年 | 1379篇 |
1993年 | 1351篇 |
1992年 | 4169篇 |
1991年 | 4206篇 |
1990年 | 3875篇 |
1989年 | 3844篇 |
1988年 | 3709篇 |
1987年 | 3556篇 |
1986年 | 3332篇 |
1985年 | 3245篇 |
1984年 | 2355篇 |
1983年 | 2044篇 |
1982年 | 1320篇 |
1979年 | 2005篇 |
1978年 | 1310篇 |
1975年 | 1259篇 |
1974年 | 1416篇 |
1973年 | 1485篇 |
1972年 | 1404篇 |
1971年 | 1281篇 |
1970年 | 1165篇 |
1969年 | 1158篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
1.
2.
3.
4.
5.
Timothy J. Cordingley Mark A.G. Wilson Kathryn M. Weston 《Health & social care in the community》2022,30(1):353-359
Vaccination is a vital health care initiative to prevent individual and population infection. To increase vaccination rates the federal government implemented the ‘No Jab, No Pay’ policy, where eligibility for several government benefits required children to be fully vaccinated by removing ‘conscientious objections’ and expanding the age range of children whose families receive benefits. This study assesses the impact of this policy at a local area within a single medical practice community in NSW, Australia. A retrospective clinical audit was performed between 2012 and 2017 on a single general practice's vaccination records for children ≤19 years. Catch-up vaccinations were assessed based on age at vaccination. Incidence of catch-up vaccinations was assessed for each of four years before and two years after the implementation of the ‘No Jab, No Pay’ policy in January 2016, along with the age of children and vaccination(s) given. Catch-up vaccinations were assessed temporally either side of implementation of ‘No Jab, No Pay’. Comparing the average annual vaccination catch-up incidence rate of 6.2% pre-implementation (2012–2015), there was an increase to 9.2% in 2016 (p < .001) and 7.8% in 2017 (p = .027). Secondary outcome measurement of catch-up vaccination incidence rates before (2012–2015) and after (2016–2017) ‘No Jab, No Pay’ implementation showed statistically significant increases for children aged 8–11 years (3.2%–5.6%, p = .038), 12–15 years (7.5%–14.7%, p < .001) and 16–19 years (3.3%–10.2%, p < .001) along with a statistically significant reduction in children aged 1–3 years (11.4%–6.2%, p = .015). Also, catch-up rates for DTPa significantly increased after program implementation. This study demonstrates that the Australian federal government vaccination policy ‘No Jab, No Pay’ was coincident with an increase in catch-up vaccinations within a rural NSW community served by one medical practice, especially for older children. 相似文献
6.
7.
Whitney S. Brandt Wanpu Yan Jian Zhou Kay See Tan Joseph Montecalvo Bernard J. Park Prasad S. Adusumilli James Huang Matthew J. Bott Valerie W. Rusch Daniela Molena William D. Travis Mark G. Kris Jamie E. Chaft David R. Jones 《The Journal of thoracic and cardiovascular surgery》2019,157(2):743-753.e3
Objective
Comparative survival between neoadjuvant chemotherapy and adjuvant chemotherapy for patients with cT2-4N0-1M0 non–small cell lung cancer has not been extensively studied.Methods
Patients with cT2-4N0-1M0 non–small cell lung cancer who received platinum-based chemotherapy were retrospectively identified. Exclusion criteria included stage IV disease, induction radiotherapy, and targeted therapy. The primary end point was disease-free survival. Secondary end points were overall survival, chemotherapy tolerance, and ability of Response Evaluation Criteria In Solid Tumors response to predict survival. Survival was estimated using the Kaplan–Meier method, compared using the log-rank test and Cox proportional hazards models, and stratified using matched pairs after propensity score matching.Results
In total, 330 patients met the inclusion criteria (n = 92/group after propensity-score matching; median follow-up, 42 months). Five-year disease-free survival was 49% (95% confidence interval, 39-61) for neoadjuvant chemotherapy versus 48% (95% confidence interval, 38-61) for adjuvant chemotherapy (P = .70). On multivariable analysis, disease-free survival was not associated with neoadjuvant chemotherapy or adjuvant chemotherapy (hazard ratio, 1.1; 95% confidence interval, 0.64-1.90; P = .737), nor was overall survival (hazard ratio, 1.21; 95% confidence interval, 0.63-2.30; P = .572). The neoadjuvant chemotherapy group was more likely to receive full doses and cycles of chemotherapy (P = .014/0.005) and had fewer grade 3 or greater toxicities (P = .001). Response Evaluation Criteria In Solid Tumors response to neoadjuvant chemotherapy was associated with disease-free survival (P = .035); 15% of patients receiving neoadjuvant chemotherapy (14/92) had a major pathologic response.Conclusions
Timing of chemotherapy, before or after surgery, is not associated with an improvement in overall or disease-free survival among patients with cT2-4N0-1M0 non–small cell lung cancer who undergo complete surgical resection. 相似文献8.
9.
10.
We report a Chinese family with members affected by epidermolytic ichthyosis (EI), caused by KRT gene mutations. The proband was a 14‐year‐old boy who had simultaneous appearance of nephroblastoma and epidermolytic ichthyosis (EI). Both the patient and his mother exhibited the specific clinical and pathological manifestations of EI. We analysed all exons and flanking sequences of the KRT1 and KRT10 genes using PCR, and found that the proband and his mother had a G>C transition at nucleotide position 1432 in exon 7 of KRT1, resulting in an amino acid substitution of glutamate (GAA) to glutamine (CAA) at codon 478 (E478Q). The KRT10 gene had no mutations. 相似文献