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31.
Iodinated contrast media (ICM) have become one of the major causes of drug hypersensitivity reactions (HSRs) related to increasing numbers of ICM-based radiological imaging procedures. Strategies for diagnosing and preventing ICM-induced HSRs have not been uniformly standardized yet. However, advances have been made based on the results of recent research. A previous history of hypersensitivity to ICM is the most significant risk factor for developing HSR by ICM. Avoidance of culprit agents and premedication is the main strategy to prevent recurrences of HSRs in high-risk patients. In addition, we strongly recommend identifying sensitized ICM using skin tests to determine immunoglobulin E-mediated or delayed-type allergy and to guide the choice of an alternative contrast agent. ICM provocation test procedures have been established and are helpful in selected cases. In this paper, we review how to evaluate patients who have experienced immediate or delayed HSRs caused by ICM to minimize the risk of recurrence and discuss unmet needs that require further research. 相似文献
32.
The role of HPV RNA transcription,immune response‐related gene expression and disruptive TP53 mutations in diagnostic and prognostic profiling of head and neck cancer 下载免费PDF全文
Knut Krohn Markus Kreuz Andreas Boehm Anett Reiche Ulrike Scharrer Dirk Halama Julia Bertolini Ulrike Bauer Dana Holzinger Michael Pawlita Jochen Hess Christoph Engel Dirk Hasenclever Markus Scholz Peter Ahnert Holger Kirsten Alexander Hemprich Christian Wittekind Olf Herbarth Friedemann Horn for the Leipzig Head Neck Group 《International journal of cancer. Journal international du cancer》2015,137(12):2846-2857
33.
Marc A. Brockmann Kai Gutensohn Juliane Bau Peter Kuehnl Thomas Meinertz Christian Nienaber 《Platelets》2013,24(8):443-449
Acute occlusion of stented coronary vessels still occurs in up to 3%. Acitvated platelets have been found to play a major role in the pathogenesis of these complications. We therefore analyzed the efficacy of a heparin coating of coronary stents and investigated the ex vivo efficacy of different antiplatelet drugs. Each of seven healthy volunteers was treated with each of the following medications for 7 days: ASA 100 mg/day, ASA 300 mg/day, ticlopidine 250 mg/day, and ticlopidine 500 mg/day. Three standardized in vitro silicon tubing models, one of them containing an uncoated stent, one a heparin-coated stent, and one without a stent (control) were filled with PRP and circulation was started. TOS in systems with heparin-coated stents was 2.4-times longer compared to systems with uncoated stents ( P <0.001), and 1.5-times longer compared to the control ( P <0.01). The increase of CD62p expression within the first 5 min was 2.5-times higher in systems with uncoated stents and 1.7-times higher in the control than in systems with heparin-coated stents ( P <0.05). Aggregometry revealed significant medication- and dose-dependent inhibition of platelet aggregability for all medications. Heparin-coating of coronary stents reduces their thrombogenicity significantly. ASA and ticlopidine effectively reduce platelet activation ex vivo . The used in vitro system facilitates a reproducible method to estimate the thrombogenicity of coronary stents prior to in vivo trials. 相似文献
34.
Kaare Solheim Knut A. Evensen Bjørn Høivik Steinar Karlsen Arne R. Rosseland 《Scandinavian cardiovascular journal : SCJ》2013,47(1):61-64
AbstractTwo operated cases of aorto-caval fistula due to ruptured abdominal aneurysm are reported. This is a rare and real surgical emergency and is fatal without operation. The classical symptoms of high-output failure occurring simultaneously with the findings of an expansible abdominal mass with thrill and bruit should facilitate clinical diagnosis. 相似文献
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Knut Gjesdal 《Scandinavian cardiovascular journal : SCJ》2013,47(3):183-186
Hospital volume and often also operator volume have documented impacts on the quality of care for aortic and aortocoronary bypass surgery, for percutaneous angioplasty and for radiofrequency ablation for arrhythmias, whereas data are less consistent for treatment of acute myocardial infarction. A review of this research is given. In the Nordic countries hospitals are small, and often the plateau of the learning curve cannot be reached. To discourage low-volume centers from embarking upon too complicated interventional or surgical procedures, the author suggests that a minimal number should be set for certain major procedures, both for hospitals and for physicians. 相似文献
39.
Josephine Prener Holtan Knut Teigen Ingvild Aukrust Ragnheiður Bragadóttir Gunnar Houge 《Ophthalmic genetics》2019,40(2):124-128
Purpose: To clinically and genetically characterise a second family with dominant ARL3-related retinitis pigmentosa due to a specific ARL3 missense variant, p.(Tyr90Cys).Methods: Clinical examination included optical coherence tomography, electroretinography, and ultra-wide field retinal imaging with autofluorescence. Retrospective data were collected from the registry of inherited retinal diseases at Oslo university hospital. DNA was analysed by whole-exome sequencing and Sanger sequencing. The ARL3 missense variant was visualized in a 3D-protein structure.Results: The phenotype was non-syndromic retinitis pigmentosa with cataract associated with early onset of decreased central vision and central retinal thinning. Sanger sequencing confirmed the presence of a de novo ARL3 missense variant p.(Tyr90Cys) in the index patient and his affected son. We did not find any other cases with rare ARL3 variants in a cohort of 431 patients with retinitis pigmentosa-like disease. By visualizing Tyr90 in the 3D protein structure, it seems to play an important role in packing of the α/β structure of ADP-ribosylation factor-like 3 (ARL3). When changing Tyr90 to cysteine, we observe a loss of interactions in the core of the α/β structure that is likely to affect folding and stability of ARL3.Conclusion: Our study confirms that the ARL3 missense variant p.(Tyr90Cys) causes retinitis pigmentosa. In 2016, Strom et al. reported the exact same variant in a mother and two children with RP, labelled ?RP83 in the OMIM database. Now the questionmark can be removed, and ARL3 should be added to the list of genes that may cause non-syndromic dominant retinitis pigmentosa. 相似文献
40.
Govind K Makharia Chris J J Mulder Khean Lee Goh Vineet Ahuja Julio C Bai Carlo Catassi Peter H R Green Siddhartha Datta Gupta Knut E A Lundin Balakrishnan Siddartha Ramakrishna Ramakant Rawat Hanish Sharma Ajit Sood Chikako Watanabe Peter R Gibson World Gastroenterology Organization‐Asia Pacific Association of Gastroenterology Working Party on Celiac Disease 《Journal of gastroenterology and hepatology》2014,29(4):666-677