全文获取类型
收费全文 | 1004篇 |
免费 | 84篇 |
国内免费 | 5篇 |
专业分类
耳鼻咽喉 | 8篇 |
儿科学 | 48篇 |
妇产科学 | 32篇 |
基础医学 | 124篇 |
口腔科学 | 42篇 |
临床医学 | 117篇 |
内科学 | 179篇 |
皮肤病学 | 23篇 |
神经病学 | 47篇 |
特种医学 | 28篇 |
外科学 | 87篇 |
综合类 | 22篇 |
预防医学 | 59篇 |
眼科学 | 69篇 |
药学 | 116篇 |
中国医学 | 9篇 |
肿瘤学 | 83篇 |
出版年
2024年 | 6篇 |
2023年 | 25篇 |
2022年 | 74篇 |
2021年 | 109篇 |
2020年 | 43篇 |
2019年 | 68篇 |
2018年 | 67篇 |
2017年 | 63篇 |
2016年 | 66篇 |
2015年 | 66篇 |
2014年 | 92篇 |
2013年 | 75篇 |
2012年 | 92篇 |
2011年 | 73篇 |
2010年 | 41篇 |
2009年 | 21篇 |
2008年 | 29篇 |
2007年 | 26篇 |
2006年 | 17篇 |
2005年 | 16篇 |
2004年 | 8篇 |
2003年 | 7篇 |
2002年 | 6篇 |
2001年 | 1篇 |
1999年 | 1篇 |
1998年 | 1篇 |
排序方式: 共有1093条查询结果,搜索用时 18 毫秒
71.
Mammographic density does not correlate with Ki-67 expression or cytomorphology in benign breast cells obtained by random periareolar fine needle aspiration from women at high risk for breast cancer 下载免费PDF全文
Background
Ki-67 expression is a possible risk biomarker and is currently being used as a response biomarker in chemoprevention trials. Mammographic breast density is a risk biomarker and is also being used as a response biomarker. We previously showed that Ki-67 expression is higher in specimens of benign breast cells exhibiting cytologic atypia that are obtained by random periareolar fine needle aspiration (RPFNA). It is not known whether there is a correlation between mammographic density and Ki-67 expression in benign breast ductal cells obtained by RPFNA. 相似文献72.
73.
74.
Prasad Sulkshane Sagar N. Pawar Rohit Waghole Sushil S. Pawar Priyanka Rajput Abhay Uthale Swapnil Oak Prajakta Kalkar Harshada Wani Rahul Patil Sudhir Nair Pallavi Rane Tanuja Teni 《British journal of cancer》2021,125(4):547
Background Overexpression of anti-apoptotic MCL-1 protein in oral squamous cell carcinoma (OSCC) is linked to disease progression, therapy resistance and poor outcome. Despite its characteristic short half-life owing to ubiquitin–proteasome-dependent degradation, oral tumours frequently show elevated MCL-1 protein expression. Hence, we investigated the role of deubiquitinase USP9X in stabilising MCL-1 protein and its contribution to oral tumorigenesis.Methods Expression of MCL-1 and USP9X was assessed by immunoblotting and immunohistochemistry in oral cancer cell lines and tissues. The association between MCL-1 and USP9X was confirmed by coimmunoprecipitation and immunofluorescence. Cell death assessment was performed by MTT, flow cytometry and clonogenic assays.Results Both USP9X and MCL-1 are significantly elevated in oral premalignant lesions and oral tumours versus normal mucosa. USP9X interacts with and deubiquitinates MCL-1, thereby stabilising it. Pharmacological inhibition of USP9X potently induced cell death in OSCC cells in vitro and in vivo. The elevated expression of USP9X and MCL-1 correlated with poor prognosis in OSCC patients.Conclusion We demonstrate the oncogenic role of USP9X in driving early-to-late stages of oral tumorigenesis via stabilisation of MCL-1, suggesting its potential as a prognostic biomarker and therapeutic target in oral cancers.Subject terms: Oral cancer detection, Oral cancer detection 相似文献
75.
76.
77.
Priyanka Anand MBBS MPH Sebastian Schneeweiss MD ScD Arash Mostaghimi MD MPA MPH Maria C. Schneeweiss MD 《Pediatric dermatology》2023,40(1):132-134
In our cohort study, we sought to describe the utilization patterns of systemic immunomodulators in children with atopic dermatitis (AD) and how utilization changed after approval of dupilumab, the first systemic drug approved for the treatment of AD. Using US nationwide claims data, we identified children with AD who initiated a systemic therapy (dupilumab, cyclosporine, methotrexate, azathioprine, and mycophenolate mofetil) from March 2015 to February 2021 and used Sankey plots to describe patterns of starting, switching, and discontinuing these drugs. Dupilumab use among children increased from 19.4% before approval in children to 88.3% after approval in 2019–20. Adherence to dupilumab may suggest better tolerance and improved outcomes in children with AD. 相似文献
78.
Wenjun Kou Priyanka Soni Matthew W. Klug Mozziyar Etemadi Peter J. Kahrilas John E. Pandolfino Dustin A. Carlson 《Neurogastroenterology and motility》2023,35(7):e14549
Background
Functional lumen imaging probe (FLIP) Panometry is performed at the time of sedated endoscopy and evaluates esophageal motility in response to distension. This study aimed to develop and test an automated artificial intelligence (AI) platform that could interpret FLIP Panometry studies.Methods
The study cohort included 678 consecutive patients and 35 asymptomatic controls that completed FLIP Panometry during endoscopy and high-resolution manometry (HRM). “True” study labels for model training and testing were assigned by experienced esophagologists per a hierarchical classification scheme. The supervised, deep learning, AI model generated FLIP Panometry heatmaps from raw FLIP data and based on convolutional neural networks assigned esophageal motility labels using a two-stage prediction model. Model performance was tested on a 15% held-out test set (n = 103); the remainder of the studies were utilized for model training (n = 610).Key Results
“True” FLIP labels across the entire cohort included 190 (27%) “normal,” 265 (37%) “not normal/not achalasia,” and 258 (36%) “achalasia.” On the test set, both the Normal/Not normal and the achalasia/not achalasia models achieved an accuracy of 89% (with 89%/88% recall, 90%/89% precision, respectively). Of 28 patients with achalasia (per HRM) in the test set, 0 were predicted as “normal” and 93% as “achalasia” by the AI model.Conclusions
An AI platform provided accurate interpretation of FLIP Panometry esophageal motility studies from a single center compared with the impression of experienced FLIP Panometry interpreters. This platform may provide useful clinical decision support for esophageal motility diagnosis from FLIP Panometry studies performed at the time of endoscopy. 相似文献79.
80.
Quality of life (QoL) encompasses the physical, psychosocial, social and spiritual dimensions of life lived by a person. Cancer pain is one of the physical component has tremendous impact on the QoL of the patient. Cancer pain is multifaceted and complex to understand and managing cancer pain involves a tool box full of pharmacological and non pharmacological interventions but still there are 50-70% of cancer patients who suffer from uncontrolled pain and they fear pain more than death. Aggressive surgeries, radiotherapy and chemotherapy focus more on prolonging the survival of the patient failing to realize that the QoL lived also matters equally. This paper reviews complementary and alternative therapy approaches for cancer pain and its impact in improving the QoL of cancer patients. 相似文献