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91.
92.
探讨青年缺血性卒中患者的血压特点。选取绵阳市中心医院2013年2月至2014年2月收治的缺血性卒中患者624例,按照年龄分为青年(年龄≤44岁)缺血性卒中172例和老年(年龄>60岁)缺血性卒中患者452例。分别在青年组和老年组内按照有无高血压分为合并高血压及非高血压。并测24 h动态血压,分别测血脂、糖化血红蛋白、同型半胱氨酸等生化指标及收集年龄、性别、吸烟史、饮食特点等流行病学资料。高血压病为青年缺血性卒中患者的重要危险因素,青年缺血性卒中患者危险因素及不良生活方式较多,有高血压患者以舒张压升高为主,男性多于女性,血压以夜间升高为主,并具有盐敏感性。青年缺血性卒中有其自身特点,应根据这些特点对缺血性卒中进行研究和治疗。 相似文献
93.
目的了解重庆市彭水县0~2岁婴幼儿喂养现状,探讨其影响因素。方法采用方便抽样,对重庆市彭水县县城中7个社区及8个乡镇中606名0~2岁婴幼儿的母乳喂养情况和半固体食物引入时间进行问卷调查,调查数据录入Epidata3.1数据库,采用SPSS19.0软件进行统计分析。结果 4月龄内婴儿纯母乳喂养率为63.6%,6月龄内婴儿纯母乳喂养率为35.3%,63.9%的婴幼儿在出生24h后开奶。大部分婴幼儿蔬菜、水果、谷类、蛋类、豆类、禽畜类、鱼类添加过晚。多因素Logistic回归分析显示,婴幼儿居住地为乡镇,开奶时间较早,是婴儿4月龄内纯母乳喂养的保护因素;喂养人年龄40岁,母乳喂养知识得分优秀者,是婴儿4月龄内纯母乳喂养的危险因素。结论调查地区婴幼儿喂养中开奶不及时,纯母乳喂养率和持续时间有待提高,半固体食物添加月龄不合理,添加过晚现象严重,应向家长提供正确喂养婴幼儿知识指导。 相似文献
94.
Building an online community to promote communication and collaborative learning between health professionals and young people who self‐harm: an exploratory study 下载免费PDF全文
Christabel Owens MA PhD Siobhan Sharkey BA PhD Janet Smithson BA PhD Elaine Hewis BA Tobit Emmens MSc Tamsin Ford MRCPsych PhD Ray Jones BSc MSc PhD 《Health expectations》2015,18(1):81-94
Background
Online communities are known to break down barriers between supposed experts and non‐experts and to promote collaborative learning and ‘radical trust’ among members. Young people who self‐harm report difficulties in communicating with health professionals, and vice versa.Aim
We sought to bring these two groups together online to see how well they could communicate with each other about self‐harm and its management, and whether they could agree on what constituted safe and relevant advice.Methods
We allocated 77 young people aged 16–25 with experience of self‐harm and 18 recently/nearly qualified professionals in relevant health‐care disciplines to three separate Internet discussion forums. The forums contained different proportions of professionals to young people (none; 25%; 50% respectively) to allow us to observe the effect of the professionals on online interaction.Results
The young people were keen to share their lived experience of self‐harm and its management with health professionals. They engaged in lively discussion and supported one another during emotional crises. Despite registering to take part, health professionals did not actively participate in the forums. Reported barriers included lack of confidence and concerns relating to workload, private–professional boundaries, role clarity, duty of care and accountability. In their absence, the young people built a vibrant lay community, supported by site moderators.Conclusions
Health professionals may not yet be ready to engage with young people who self‐harm and to exchange knowledge and experience in an anonymous online setting. Further work is needed to understand and overcome their insecurities. 相似文献95.
Kwame Owusu-Edusei Jr. Harrell W. Chesson Thomas L. Gift Robert C. Brunham Gail Bolan 《Emerging infectious diseases》2015,21(6):960-968
We explored potential cost-effectiveness of a chlamydia vaccine for young women in the United States by using a compartmental heterosexual transmission model. We tracked health outcomes (acute infections and sequelae measured in quality-adjusted life-years [QALYs]) and determined incremental cost-effectiveness ratios (ICERs) over a 50-year analytic horizon. We assessed vaccination of 14-year-old girls and catch-up vaccination for 15–24-year-old women in the context of an existing chlamydia screening program and assumed 2 prevaccination prevalences of 3.2% by main analysis and 3.7% by additional analysis. Estimated ICERs of vaccinating 14-year-old girls were $35,300/QALY by main analysis and $16,200/QALY by additional analysis compared with only screening. Catch-up vaccination for 15–24-year-old women resulted in estimated ICERs of $53,200/QALY by main analysis and $26,300/QALY by additional analysis. The ICER was most sensitive to prevaccination prevalence for women, followed by cost of vaccination, duration of vaccine-conferred immunity, and vaccine efficacy. Our results suggest that a successful chlamydia vaccine could be cost-effective. 相似文献
96.
Multidisciplinary diabetes team care: the experiences of young adults with Type 1 diabetes 下载免费PDF全文
Janice Wiley MB BS MPH MHM Mary Westbrook PhD Janet Long RN Jerry R. Greenfield PhD Richard O. Day MD Jeffrey Braithwaite PhD 《Health expectations》2015,18(5):1783-1796
Background
This research examined whether young adults with Type 1 diabetes engage with the multidisciplinary consultation process and if not, then why.Methods
We designed a web‐based self‐reported survey, available online from February to May 2011, for Australian adults 18–35 years with Type 1 diabetes. Respondents were asked about which clinicians they consulted to assist with self‐management. To expand on the results of the survey, we interviewed 33 respondents.Results
Survey: Respondents (n = 150) consulted with the following clinicians: endocrinologist and diabetes educators: 23.3%; endocrinologist only: 18.0%; endocrinologist, diabetes educators and dieticians: 14.6%; endocrinologist, diabetes educators, dietician and general practitioners (GP): 11.3%; endocrinologist and GP: 10.6%; GP only: 4.6%; all clinicians recommended to assist with self‐management: 1.3%; 2.7% did not consult any clinician. Interview: Participants (n = 33) reported eight key disincentives to consultation with multidisciplinary clinicians. These were time constraints; provision of conflicting advice; inaccessibility of health services; variation in service standards; cost constraints; failure of clinicians to refer to other clinicians; lack of opportunity to build a therapeutic relationship; and failure of clinicians to engage in shared decision making.Conclusion
Our results indicate that high attrition rates of young adults with Type 1 diabetes from recommended diabetes health services is linked to the failure of those services to meet the needs and preferences of their patients. The identified needs and preferences included joint consultation with multi‐disciplinary team clinicians; flexible access to advice by email or telephone consultation; and shared decision making. Patient engagement in health‐service re‐design has implications for improved health‐service delivery and enhanced treatment outcomes. 相似文献97.
Attitudes to weight and weight management in the early teenage years: a qualitative study of parental perceptions and views 下载免费PDF全文
Background
As most young teenagers grow up in families, parents might be well situated to facilitate and support their weight management and thereby prevent or manage obesity prior to adulthood.Aim
This paper explores parents'' perceptions of, and views about, their teenage children''s weight and the factors that influence parents'' weight management strategies.Design, setting and participants
We conducted two qualitative studies in Scotland, UK, involving in‐depth interviews with the parents of overweight/obese and ‘normal’ weight 13–15 year olds (n = 69).Findings
Parents'' concerns about their own weight provided useful context for understanding their attitudes or actions with regards to their teenage child. Some parents described their teenager''s weight as being of concern to them, although puberty often introduced confusion about a child''s weight status. Genetic explanations were very often put forward as a way of making sense of teenage weight or body size. Frustration about advising teenagers about weight management was expressed, and some parents worried about giving their growing child a ‘problem’ if they directly raised concerns about weight with them.Discussion
Parents'' views about their own weight as well as social and moral norms about labelling a teenager as overweight or as needing help with their weight could usefully inform patient‐centred service development. Parent/teenage partnerships and supporting parents to create a healthy home in which teenagers can make healthier choices are suggestions for intervention development.Conclusion
The study highlights the importance of taking parents'' perceptions into account when developing family‐based interventions to address teenage overweight and obesity. 相似文献98.
Excessive recreational noise exposure in young adults might result in noise-induced hearing loss (NIHL) and tinnitus. Inducing behavioral change in young adults is one of the aims of a hearing conservation program (HCP). The goal of the current study was to evaluate the effect of a hearing education program after 6 months in young adults in relation to knowledge regarding their individual hearing status. The results of a questionnaire regarding the weekly equivalent recreational noise exposure, attitudes and beliefs toward noise, and hearing loss and hearing protector devices (HPDs) were compared between both sessions. Seventy-eight young adults completed the questionnaire concerning recreational noise exposure, youth attitude to noise scale (YANS), and beliefs about hearing protection and hearing loss (BAHPHL). Their hearing status was evaluated based on admittance measures, audiometry, transient-evoked otoacoustic emissions (TEOAEs), and distortion-product otoacoustic emissions (DPOAEs). The main analysis consisted of a mixed model analysis of variance with dependent variables of either the noise exposure or the scores on (subscales of) YANS and BAHPHL. The independent variables were hearing status and session one versus session two. There was a significant decrease in recreational noise exposure and several (sub) scales of YANS and BAHPHL between both the sessions. This behavioral change resulted in a more frequent use of HPDs in 12% of the participants. However, the behavioral change was not completely related to the knowledge of young adults’ individual hearing status. To prevent hearing damage in young people, investing in HCPs is necessary, apart from regulating sound levels and its compliance at various leisure-time activities. Also, the long-term effect of HCPs and their most cost-efficient repetition rates should be further investigated. 相似文献
99.
Tina Lam Simon R. Lenton Lucinda Burns Alexandra Aiken Rowan Ogeil William T. Gilmore Tanya N. Chikritzhs Belinda Lloyd Dan I. Lubman Richard Mattick Steve J. Allsop 《Australian and New Zealand journal of public health》2015,39(2):129-134
Objective: To explore the impacts of existing policies on young Australian risky drinkers' access to alcohol and to gauge their support for proposed alcohol measures. Methods: The 16–19 year old participants were recruited from three Australian states using non‐random convenience sampling, for either a face‐to‐face or online quantitative survey (N=958). The sample was deliberately selected to represent drinkers whose consumption placed them in the riskiest drinking 20–25% of their age bracket. Results: Half (49%) the sample who were younger than the Australian legal purchase age reported it was ‘easy’ to buy alcohol from bottle stores, and 75% of those who had tried to purchase alcohol, said it was ‘easy’ the last time they tried. Half of those under 18, who had attempted to enter a licensed venue, reported they did not have their identification checked last time they gained access. Ninety per cent of all respondents drank within a private location at their last risky drinking session. Sixty‐five per cent supported ‘increasing the price of [alcohol by 20¢] a standard drink if the extra 20¢ was used to support prevention and treatment of alcohol problems'. Conclusions: Age‐ or intoxication‐based restrictions to alcohol were commonly bypassed. Implications: Point‐of‐sale alcohol controls require improvement to prevent under age access. Given that a significant proportion of drinking occasions for those under 18 were in private premises, prevention strategies need to target these locations. There were diverse levels of support for strategies to reduce harm, including potential community backing for an evidence‐based proposed price policy. 相似文献
100.
Consulting with young people to inform systematic reviews: an example from a review on the effects of schools on health 下载免费PDF全文