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1.
AimsDue to the lack of high-quality evidence and consensus on adjuvant treatment for locoregionally advanced penile cancer, we reviewed the outcomes of pN3 patients to determine the suitable adjuvant treatment options.Patients and methodsAll consecutive pN3 penile cancer patients treated at our institution between January 2010 and December 2018 were reviewed to assess the impact of demographical, pathological and treatment factors on disease-free survival (DFS) and overall survival. The DFS and overall survival were estimated using the Kaplan–Meier method and association was tested using the Cox regression model (two-sided test with P < 0.05 considered significant).ResultsOf 128 patients, 31 (24%) had pelvic nodal involvement. Twenty-six patients (20.3%) received no adjuvant treatment, 40 (31.3%) received single modality adjuvant treatment and 62 (48.4%) received multimodality adjuvant treatment (a combination of chemotherapy and radiotherapy). At a median follow-up of 22 months, the DFS and overall survival were 55.4 and 62%, respectively. The best DFS and overall survival was noted with chemotherapy followed by concurrent chemoradiation (C-CTRT; 93% each). On multivariate analysis, both DFS and overall survival were worse with pelvic node involvement (2.2 [1.3–4], P = 0.027 and 2.2 [1.3–4], P = 0.027, respectively) and better with any adjuvant treatment (single modality: 3 [1.5–5.5], P < 0.001; multimodality: 3.1 [1.6–6], P < 0.001). C-CTRT was associated with improved DFS over chemotherapy alone (0.17 [0.4–0.78], P = 0.02) but not over radiotherapy alone (0.35 [0.07–1.6], P = 0.19). In patients with no pelvic nodes involved, chemotherapy and radiotherapy as single modalities were associated with similar DFS and overall survival. In patients with pelvic nodes, multimodality treatment was associated with better DFS than single modality treatment (0.3 [0.1–1], P = 0.05).Conclusion: pN3 penile cancer is a diverse prognostic group with poorer outcomes associated with pelvic nodes. Single modality adjuvant treatment may be adequate in inguinal nodes with extranodal extension, but multimodality treatment should be given in patients with pelvic nodal involvement.  相似文献   
2.
目的:比较HyperArc、容积旋转调强(VMAT)和射波刀(CyberKnife)在单发和多发脑转移瘤(BM)放射治疗中的剂量学差异。方法:将75例脑转移瘤CT图像分成5组(1 BM、4 BM、8 BM、15 BM、20 BM),分别设计HyperArc、非共面VMAT和CyberKnife这3种不同技术(HA、nCO-VMAT、CK)的计划。分析比较3种计划的剂量学差异,包括靶区适形度指数(CI)、梯度指数(GI)、正常脑组织平均剂量(Brainmean)、机器总跳数(MU)以及出束时间。结果:在1 BM中,HA、nCO-VMAT、CK的GI值(P=0.429)和Brainmean值(P=0.799)接近;HA和nCO-VMAT的CI值接近,优于CK(P<0.001)。在4 BM中,HA、nCO-VMAT、CK的GI值(P=0.334)和Brainmean值(P=0.317)都接近;HA和nCO-VMAT的CI值接近,优于CK(P<0.001)。在8 BM中,HA和nCO-VMAT的CI值接近,优于CK(P<0.001);HA和CK的GI值接近,优于nCO-VMAT(P<0.001)。在15 BM中,HA的CI值(P<0.001)最优;CK的GI值(P<0.001)最优,HA次之,nCO-VMAT最差;CK的Brainmean值(P<0.001)最优,HA次之,nCO-VMAT最差。在20 BM中,HA的CI值(P<0.001)最优;CK的GI值(P<0.001)最优,HA次之,nCO-VMAT最差。在所有组中HA和nCO-VMAT的MU值都比CK低,CK的出束时间都远大于HA和nCO-VMAT。结论:HA、nCO-VMAT与CK技术都可以降低正常脑组织的剂量,都能取得很好的CI和GI,但HA出束时间短,CK出束时间长。  相似文献   
3.
目的 研究胸段食管癌逆向调强放射治疗(IMRT)中累及野照射与扩大野照射对危及器官(OAR)受照剂量的影响。方法 40例胸段食管癌患者分别行累及野靶区勾画和扩大野靶区勾画并勾画危及器官,制定IMRT计划,评估2个计划的靶区适形指数(CI)和均匀性指数(HI)及危及器官的剂量学参数,剂量学参数比较采用配对t检验。结果 2种计划的PTV均能满足处方剂量要求,PTV在CIHI上相近(P = 0.317、0.130)。两组间平均肺剂量、两肺V5、两肺V20、两肺V30、脊髓Dmean、心脏Dmean、心脏Dmax、心脏V30、心脏V40、心脏V60差异均存在统计学意义(P < 0.01)。结论 胸段食管癌患者行累及野照射与扩大野比较,可降低正常器官的受照剂量,从而降低放射性损伤风险。  相似文献   
4.
《Cancer radiothérapie》2022,26(3):458-466
PurposeRadiation therapy is often the last resource treatment for cervical relapse in iodine refractory differentiated thyroid cancer. We present locoregional control data in patients with cervical relapse treated with curative intent radiation therapy with or without concomitant carboplatin.Material and methodsThis monocentric retrospective study gathered data on patients with differentiated thyroid carcinoma – vesicular or papillary – in relapse after thyroidectomy who received a curative intent cervical radiation therapy. Locoregional progression free survival (LRPFS), progression free survival (PFS), overall survival (OS) were gathered as well as acute and chronic adverse events assessed with the CTCAE v4.ResultsThirty-nine patients were consecutively included between 2005 and 2019. The median follow-up was 36.6 months. Fifteen patients (38%) had a locoregional relapse, locoregional control at 2 years was 66.7%. The median LRPFS was 48 months [32.9–not reached] and the median overall survival 49 months [38.8–not reached]. In multivariate analysis, initial incomplete resection was associated with poorer OS (HR: 24.39 [3.57–166.78], P = 0.00113) and LRPFS (HR: 33.91 [4.46–257.61], P = 0.00066), extra nodal spread was associated with poorer LRPFS (HR: 13.45 [1.81–99,76], P = 0.011). ECOG performance status was associated with OS (HR: 5.11 [1.57–16.66], P = 0.00688). Carboplatin association with radiation therapy was not associated with improved survivals (OS: P = 0.34, LRPFS: P = 0.84). The rate of acute grade 3 toxicities was 14%.ConclusionSalvage cervical radiation therapy was associated with a locoregional control of 66.7% at 2 years with a reasonable toxicity rate. Carboplatin association with radiation therapy did not improve locoregional control nor overall survival in comparison with radiotherapy alone.  相似文献   
5.
Specialized pro-resolving mediators (SPMs) are endogenous small molecules produced mainly from dietary omega-3 polyunsaturated fatty acids by both structural cells and cells of the active and innate immune systems. Specialized pro-resolving mediators have been shown to both limit acute inflammation and promote resolution and return to homeostasis following infection or injury. There is growing evidence that chronic immune disorders are characterized by deficiencies in resolution and SPMs have significant potential as novel therapeutics to prevent and treat chronic inflammation and immune system disorders. This review focuses on important breakthroughs in understanding how SPMs are produced by, and act on, cells of the adaptive immune system, specifically macrophages, B cells and T cells. We also highlight recent evidence demonstrating the potential of SPMs as novel therapeutic agents in topics including immunization, autoimmune disease and transplantation.  相似文献   
6.
目的:研究头颈部面罩和胸部体罩固定在胸上段食管癌(EC)三维放疗计划系统(TPS)放疗应用中对剂量分布的影响。方法:回顾性分析128例胸上段EC患者临床资料,根据放疗时体位固定工具不同,将患者分为面罩组46例和体罩组82例,所有患者均取仰卧位并采用调强适形放射治疗进行干预,体位固定方法为面罩组以热塑头颈面罩固定,体罩组采用热塑体膜固定,比较两组摆位误差、剂量分布、危及器官受照剂量、近期疗效和不良反应等指标。结果:面罩组X轴、Y轴和Z轴摆位误差绝对值明显低于体罩组(P<0.05),面罩组射线均匀性指数明显低于体罩组,射线适形度指数明显高于体罩组(P<0.05),两组肿瘤靶区Dmax、Dmin和Dmean比较差异无统计学意义(P>0.05);面罩组双肺V10、V20、V30以及脊髓Dmean均低于体罩组,差异有统计学意义(P<0.05);面罩组和体罩组患者客观缓解率分别为58.70%和54.88%,两组近期疗效比较差异无统计学意义(P>0.05);面罩组放射性肺炎发生率低于体罩组(P<0.05)。结论:头颈部面罩固定用于胸上段EC放疗有利于降低摆位误差,提升TPS放疗剂量分布均匀度和适形度,减少周围正常器官照射剂量和放疗相关不良反应发生。  相似文献   
7.
目的:分析基于几何不确定性的鲁棒优化计划对肝癌立体定向放疗(SBRT)剂量分布的影响。方法:选取12例肝癌SBRT患者,对每例制作3个调强计划:①基于PTV(ITV-PTV 5 mm)的常规优化(PTV-Based Plan);②基于ITV非均匀几何不确定性(本中心计算的不确定性值:进出方向7 mm,左右和前后方向4 mm)的鲁棒优化(Robust Planactual);③基于ITV均匀5 mm几何不确定性的鲁棒优化(Robust Plan5 mm)。所有计划都以95%的PTV满足处方剂量作为目标,以等中心均匀偏移4、5、7 mm计算扰动剂量评估鲁棒性。结果:计划①②③的均匀性指数(HI)分别为0.083±0.027、0.099±0.035、0.096±0.026,不具有统计学意义;计划①②③的适形性指数(CI)分别为0.98±0.02、1.02±0.05、1.00±0.04,计划②③相对于计划①的CI具有统计学意义。计划③的正常肝组织平均受量和V2500相对于计划①②分别下降了4.1%、2.5%和5.4%、3.0%,且具有统计学意义(P=0.034、P=0.021和P=0.004、P=0.004),计划②相对于计划①的正常肝组织平均受量和V2500不具有统计学意义(P=0.308和P=0.182),但下降了1.6%和2.5%。对于其鲁棒性,计划②③的5 mm-D99%、5 mm-D98%、5 mm-D95%的剂量-体积直方图带宽(DVHBW)差值相对于计划①更小,随着摆位不确定度的增大,其DVHBW差值越大。结论:在肝脏SBRT治疗中,采用鲁棒优化能够提高靶区剂量分布质量,即使在摆位不确定度有所增加的情况下,仍可以保证ITV的剂量覆盖同时不增加正常组织的照射剂量。  相似文献   
8.
癌症已成为严重威胁人类健康的主要公共卫生问题。60%~70%的癌症患者需要进行放射治疗。调强放疗是当前主要的临床放疗技术。对近几年基于深度学习的影像分析与转换方法在肿瘤调强放疗计划中的应用进展及关键技术进行综述,包括计算机断层扫描(CT)、锥形束CT(CBCT)、磁共振成像(MRI)、正电子发射断层扫描(PET)引导的肿瘤调强放疗技术应用现状与发展趋势,肿瘤CT/CBCT/MRI/PET影像放疗靶区分割、影像配准以及转换深度卷积神经网络、生成对抗网络的有监督或无监督学习方法,并对未来的研究方向进行展望。  相似文献   
9.
评估AAA、AXB算法在鼻咽癌调强放射治疗(IMRT)中剂量计算的准确性,并分析空腔和骨性结构对剂量计算准确性造成的影响,以期指导临床应用。选取20例鼻咽癌IMRT计划导入SciMoCa中,使用蒙特卡罗算法进行独立验算,以蒙特卡罗计算结果为标准,对比光子剂量算法(AAA和AXB)对靶区和危及器官的剂量差异,以及γ通过率,并分析空腔和骨性结构对剂量分布的影响。结果表明:使用AAA、AXB算法的计划平均γ通过率分别为95.99%和96.26%,无统计学差异(P>0.05)。靶区内空腔区域AAA、AXB算法的平均剂量偏差为-2.26%和-0.33%,γ通过率为80.22%和98.55%;靶区内骨性结构区域AAA、AXB算法的平均剂量偏差为1.43%和0.17%,γ通过率为93.25%和99.72%。AAA算法下靶区内空腔区域的γ通过率与其体积呈线性正比(r=0.65),靶区骨性结构区域的γ通过率与其体积呈线性反比(r=-0.74);当空腔体积<20 cm3或骨性结构体积>10 cm3时,γ通过率均<95%。使用AAA算法时需要注意靶区内空腔和骨性结构的体积对剂量计算准确性的影响,而使用AXB算法时无需考虑空腔和骨性结构体积的影响,其计算结果与蒙特卡罗算法更接近。  相似文献   
10.
ObjectiveSeveral trials have recently reported the safety of pulmonary resection after neoadjuvant immunotherapy with encouraging major pathological response rates. We report the detailed adverse events profile from a recently conducted randomized phase II trial in patients with resectable non–small cell lung cancer treated with neoadjuvant durvalumab alone or with sub-ablative radiation.MethodsWe conducted a randomized phase II trial in patients with non–small cell lung cancer clinical stages I to IIIA who were randomly assigned to receive neoadjuvant durvalumab alone or with sub-ablative radiation (8Gyx3). Secondary end points included the safety of 2 cycles of preoperative durvalumab with and without radiation followed by pulmonary resection. Postoperative adverse events within 30 days were recorded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 4.0).ResultsSixty patients were enrolled and randomly assigned, with planned resection performed in 26 patients in each arm. Baseline demographics and clinical variables were balanced between groups. The median operative time was similar between arms: 128 minutes (97-201) versus 146 minutes (109-214) (P = .314). There was no 30- or 90-day mortality. Grade 3/4 adverse events occurred in 10 of 26 patients (38%) after monotherapy and in 10 of 26 patients (38%) after dual therapy. Anemia requiring transfusion and hypotension were the 2 most common adverse events. The median length of stay was similar between arms (5 days vs 4 days, P = .172).ConclusionsIn this randomized trial, the addition of sub-ablative focal radiation to durvalumab in the neoadjuvant setting was not associated with increased mortality or morbidity compared with neoadjuvant durvalumab alone.  相似文献   
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