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The association between kidney function and cancer incidence is inconsistent among previous reports, and data on the Japanese population are lacking. It is unknown whether kidney function modifies the cancer risk of other factors. We aimed to evaluate the association of estimated glomerular filtration rate (eGFR) with cancer incidence and mortality in 55 242 participants (median age, 57 years; 55% women) from the Japan Multi-Institutional Collaborative Cohort Study. We also investigated differences in cancer risk factors between individuals with and without kidney dysfunction. During a median 9.3-year follow-up period, 4278 (7.7%) subjects developed cancer. Moderately low and high eGFRs were associated with higher cancer incidence; compared with eGFR of 60-74 ml/min/1.73 m2, the adjusted hazard ratios (HRs) (95% confidence intervals [CIs]) for eGFRs of ≥90, 75-89, 45-59, 30-44 and 10-29 ml/min/1.73 m2 were 1.18 (1.07-1.29), 1.09 (1.01-1.17), 0.93 (0.83-1.04), 1.36 (1.00-1.84) and 1.12 (0.55-2.26), respectively. High eGFR was associated with higher cancer mortality, while low eGFR was not; the adjusted subdistribution HRs (95% CIs) for eGFRs of ≥90 and 75-89 ml/min/1.73 m2 were 1.58 (1.29-1.94) and 1.27 (1.08-1.50), respectively. Subgroup analyses of participants with eGFRs ≥60 and <60 ml/min/1.73 m2 revealed elevated cancer risks of smoking and family history of cancer in those with eGFR <60 ml/min/1.73 m2, with significant interactions. Our findings suggest that the relationship between eGFR and cancer incidence was U-shaped. Only high eGFR was associated with cancer mortality. Kidney dysfunction enhanced cancer risk from smoking.  相似文献   
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分级诊疗制度是优化基本医疗卫生制度的重要步骤,但落地实施时遇到阻碍,因存在转诊标准不一、空间不连贯和时间滞后等问题,医联体模式推进存在难度。上海市浦东新区人民医院联合7家社区卫生服务中心,构建了一套以信息化为支撑的川沙医联体慢性肾脏病(CKD)专病精准分级诊疗管理方案。以CKD病种为例,基于指南梳理CKD患者的疾病管理规律,建立医疗信息联通共享、转诊规则标准的CKD专病分级诊疗知识库,设计区域CKD专病分级诊疗系统,构建了基于医院-社区联动管理的专病分级诊疗一体化管理模型。且实证应用评价显示,基于CKD知识库的专病分级诊疗模式,可以精准定位易发和高危人群,及时筛查评估CKD早期患者,提升CKD患者的健康管理和诊疗效率。  相似文献   
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Acute kidney injury (AKI) and chronic kidney disease (CKD) are posing great threats to global health within this century. Studies have suggested that estrogen and estrogen receptors (ERs) play important roles in many physiological processes in the kidney. For instance, they are crucial in maintaining mitochondrial homeostasis and modulating endothelin-1 (ET-1) system in the kidney. Estrogen takes part in the kidney repair and regeneration via its receptors. Estrogen also participates in the regulation of phosphorus homeostasis via its receptors in the proximal tubule. The ERα polymorphisms have been associated with the susceptibilities and outcomes of several renal diseases. As a consequence, the altered or dysregulated estrogen/ERs signaling pathways may contribute to a variety of kidney diseases, including various causes-induced AKI, diabetic kidney disease (DKD), lupus nephritis (LN), IgA nephropathy (IgAN), CKD complications, etc. Experimental and clinical studies have shown that targeting estrogen/ERs signaling pathways might have protective effects against certain renal disorders. However, many unsolved problems still exist in knowledge regarding the roles of estrogen and ERs in distinct kidney diseases. Further research is needed to shed light on this area and to enable the discovery of pathway-specific therapies for kidney diseases.  相似文献   
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于大君  翁维良  陆芳  高蕊  李睿 《中医杂志》2012,53(3):222-224
目的 通过对慢性肾脏病(CKD)Ⅲ期病例的中医个体化治疗,研究单病例随机对照试验在中医药临床研究中的可行性.方法 按照CKD分期标准纳入患者,合格病例采用单病例随机对照设计,每个病例研究共分为3轮,每轮为2期,即治疗期和对照期,每期为4周.每一轮以计算机随机数字法简单随机分组,拟定随机化方案,治疗期采用中医辨证治疗和常规基础治疗,对照期采用常规基础治疗,疗效指标为主要症状积分、血肌酐(SCr)和肌酐清除率(Ccr).每天由患者在固定时间记录症状分值,实验室指标试验前和每期试验后各记录1次.结果 共纳入CKD病例3例,3例患者中医症状积分在每轮均有不同程度的改善,其中1例部分改善,2例全部改善.3例患者每轮治疗期与对照期相比,SCr有不同程度的下降,Ccr有不同程度的升高,治疗期均好于对照期.3例患者全部3轮治疗期与对照期SCr和Ccr的数据合并后,显示差异有统计学意义.结论 单病例随机对照试验的研究方法能体现中医个体化的优势,该设计方案应用于中医药临床研究具有可行性.  相似文献   
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中药延缓慢性肾脏病进展的机制   总被引:5,自引:1,他引:5  
慢性肾脏病(chronic kidney disease,CKD)进展的病理基础包括肾小球硬化、肾间质纤维化和肾动脉硬化,这些病理改变与足细胞及其相关膜蛋白结构或表达异常、尿蛋白肾毒性、肾素.血管紧张素-醛固酮系统活性增强、致纤维化细胞因子过度表达、肾小管上皮细胞表型转化,以及高脂血症、高血压等因素有关.中药可以改善影响肾小球硬化、肾间质纤维化和肾动脉硬化的增恶因素,从而,延缓CKD进展.  相似文献   
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Chronic kidney disease (CKD) is an incurable disease in which renal function gradually declines, resulting in no noticeable symptoms during the early stages and a life-threatening disorder in the latest stage. The changes that accompany renal failure are likely to influence the gut microbiota, or the ecosystem of micro-organisms resident in the intestine. Altered gut microbiota can display metabolic changes and become harmful to the host. To study the gut–kidney axis in vivo, animal models should ideally reproduce the disorders affecting both the host and the gut microbiota. Murine models of CKD, but not dog, manifest slowed gut transit, similarly to patient. Animal models of CKD also reproduce altered intestinal barrier function, as well as the resulting leaky gut syndrome and bacterial translocation. CKD animal models replicate metabolic but not compositional changes in the gut microbiota. Researchers investigating the gut–kidney axis should pay attention to the selection of the animal model (disease induction method, species) and the setting of the experimental design (control group, sterilization method, individually ventilated cages) that have been shown to influence gut microbiota.  相似文献   
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