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排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
Kara S. Tanaka MD Veronica R. Andaya BA Steven W. Thorpe MD Kenneth R. Gundle MD James B. Hayden MD Yee-Cheen Duong MD Raffi S. Avedian MD David G. Mohler MD Lee J. Morse MD Melissa N. Zimel MD Richard J. O'Donnell MD Andrew Fang MD Robert Lor Randall MD Tina H. Tran BS Christin New BA Rosanna L. Wustrack MD other members of Study Group FORCE 《Journal of surgical oncology》2023,127(1):148-158
2.
S. Liu A. E. Patanwala J. M. Naylor N. Levy R. Knaggs J. A. Stevens B. Bugeja D. Begley K. E. Khor E. Lau R. Allen S. Adie J. Penm 《Anaesthesia》2023,78(10):1237-1248
Modified-release opioids are often prescribed for the management of moderate to severe acute pain following total hip and knee arthroplasty, despite recommendations against their use due to increasing concerns regarding harm. The primary objective of this multicentre study was to examine the impact of modified-release opioid use on the incidence of opioid-related adverse events compared with immediate-release opioid use, among adult inpatients following total hip or knee arthroplasty. Data for total hip and knee arthroplasty inpatients receiving an opioid analgesic for postoperative analgesia during hospitalisation were collected from electronic medical records of three tertiary metropolitan hospitals in Australia. The primary outcome was the incidence of opioid-related adverse events during hospital admission. Patients who received modified with or without immediate-release opioids were matched to those receiving immediate-release opioids only (1:1) using nearest neighbour propensity score matching with patient and clinical characteristics as covariates. This included total opioid dose received. In the matched cohorts, patients given modified-release opioids (n = 347) experienced a higher incidence of opioid-related adverse events overall, compared with those given immediate-release opioids only (20.5%, 71/347 vs. 12.7%, 44/347; difference in proportions 7.8% [95%CI 2.3–13.3%]). Modified-release opioid use was associated with an increased risk of harm when used for acute pain during hospitalisation after total hip or knee arthroplasty. 相似文献
3.
目的 探讨血管内超声虚拟组织学成像(VH-IVUS)与实时剪切弹性成像技术(SWE)评估颈动脉斑块稳定性及脑梗死的价值。方法 选取2018年12月~2020年12月在中国人民解放军联勤保障部队第960医院就诊的颈动脉粥样硬化斑块患者130例(201个斑块),分析不同性质斑块VH-IVUS评分及平均杨氏模量差异,及评估稳定性斑块的价值。130例颈动脉粥样硬化斑块患者近期发生脑梗死53例(脑梗死组),无脑梗死77例(无脑梗死组),比较两组甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、VH-IVU评分及平均杨氏模量水平,同时分析VH-IVUS评分及平均杨氏模量评估脑梗死的价值。结果 易损性斑块VH-IVUS评分高于稳定性斑块(P<0.05),而平均杨氏模量低于稳定性斑块(P<0.05);VH-IVUS评分、平均杨氏模量评估稳定性斑块的ROC曲线下面积分别为0.789和0.875。脑梗死组TG、LDL-C明显高于无脑梗死组(P<0.05),而HDL-C明显低于无脑梗死组(P<0.05);脑梗死组斑块VH-IVUS评分明显高于无脑梗死组(P<0.05),而平均杨氏模量明显低于无脑梗死组(P<0.05);VH-IVUS评分、平均杨氏模量评估脑梗死的ROC曲线下面积分别为0.658和0.822。结论 VH-IVUS与SWE技术评估颈动脉斑块稳定性及脑梗死方面有较好的价值,其中SWE评估价值较高。 相似文献
4.
目的了解临床护士工作自主性与行为目标达成度现状,并探讨两者的相关性,为提高护士行为目标达成度提供参考。方法以方便抽样法选取临床护士286名,采用工作自主性量表、护士行为目标达成度量表进行调查。结果临床护士工作自主性得分为(5.16±1.45)分,行为目标达成度得分为(4.22±0.69)分;工作自主性与行为目标达成度呈正相关(P<0.01);多元回归分析结果显示,护理层级、婚姻状况和工作自主性是护士行为目标达成度的主要影响因素(P<0.05,P<0.01)。结论临床护士的工作自主性和行为目标达成度均处于较高水平,临床护士工作自主性越高,其行为目标达成度越好。护理管理者应重视培养护士的工作自主性,挖掘护士的工作潜能,提高护士行为目标达成度,提升优质护理服务质量。 相似文献
5.
International Ophthalmology - To report a series of patients who developed neurotrophic keratopathy following scleral fixation of intraocular lenses. Retrospective case series of patients... 相似文献
6.
Polyakova E. B. Sabirzyanov D. R. Prozorova N. A. Foteeva A. B. 《Pharmaceutical Chemistry Journal》2022,55(10):1119-1125
Pharmaceutical Chemistry Journal - Metformin hydrochloride is widely used to treat diabetes mellitus. This review presents its physical and chemical properties and discusses methods of analysis... 相似文献
7.
Marco N. Iannone Stefano Stucchi Elia A. Turolla Chiara Beretta Samuele Ciceri Clizia Chinello Lisa Pagani Sergio Todde Patrizia Ferraboschi 《Journal of labelled compounds & radiopharmaceuticals》2022,65(3):48-62
In the last decade, the development of new radiopharmaceuticals for the imaging and therapy of prostate cancer has been a highly active and important area of research, especially focusing on the prostate-specific membrane antigen (PSMA), an antigen which is upregulated in prostate, as well as in other tumor cells. A large variety of PSMA ligands have been radiolabeled, to date. Among the various derivatives, PSMA-617 resulted to be one of the most interesting in terms of interaction with the antigen and clinical properties, and its lutetium-177 labeled version has recently been approved by regulatory agencies for therapeutic purposes. For this reasons, the radiolabeling with fluorine-18 of a PSMA-617 derivative might be of interest. Beside other methodologies to radiolabel macromolecules with fluorine-18, the “click-chemistry” approach resulted to be very useful, and the copper-catalyzed azide-alkyne cycloaddition (CuAAC) is considered one of most efficient and reliable. This paper proposes the synthesis of a suitable precursor for the radiolabeling with fluorine-18 of a new PSMA-617 derivative. The whole radiosynthetic procedure has been fully automated, and the final product, which proved to be stable in plasma, has been obtained with radiochemical yield and purity suitable for subsequent preclinical studies. 相似文献
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10.
Silvia Radenkovic Diego Martinelli Yuebo Zhang Graeme J. Preston Arianna Maiorana Alessandra Terracciano Maria Lisa Dentici Elisa Pisaneschi Antonio Novelli Wasantha Ranatunga Anna N. Ligezka Bart Ghesquière David R. Deyle Tamas Kozicz Filippo Pinto e Vairo Peter Witters Eva Morava 《Genetics in medicine》2022,24(4):894-904
PurposeTRAPPC9 deficiency is an autosomal recessive disorder mainly associated with intellectual disability (ID), microcephaly, and obesity. Previously, TRAPPC9 deficiency has not been associated with biochemical abnormalities.MethodsExome sequencing was performed in 3 individuals with ID and dysmorphic features. N-Glycosylation analyses were performed in the patients’ blood samples to test for possible congenital disorder of glycosylation (CDG). TRAPPC9 gene, TRAPPC9 protein expression, and N-glycosylation markers were assessed in patient fibroblasts. Complementation with wild-type TRAPPC9 and immunofluorescence studies to assess TRAPPC9 expression and localization were performed. The metabolic consequences of TRAPPC9 deficiency were evaluated using tracer metabolomics.ResultsAll 3 patients carried biallelic missense variants in TRAPPC9 and presented with an N-glycosylation defect in blood, consistent with CDG type I. Extensive investigations in patient fibroblasts corroborated TRAPPC9 deficiency and an N-glycosylation defect. Tracer metabolomics revealed global metabolic changes with several affected glycosylation-related metabolites.ConclusionWe identified 3 TRAPPC9 deficient patients presenting with ID, dysmorphic features, and abnormal glycosylation. On the basis of our findings, we propose that TRAPPC9 deficiency could lead to a CDG (TRAPPC9-CDG). The finding of abnormal glycosylation in these patients is highly relevant for diagnosis, further elucidation of the pathophysiology, and management of the disease. 相似文献