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1.
持续皮下胰岛素输注对2型糖尿病早期胰岛功能改善作用的临床研究 总被引:1,自引:0,他引:1
目的探讨初发的2型糖尿病患者,应用持续皮下胰岛素输注(CSII)或多次胰岛素皮下注射(MSII)的治疗,对胰岛β细胞功能和血糖的影响。方法CSII组采用持续皮下胰岛素输注形式,在3天内使血糖达标;MSII组采用小剂量起步,平均2~3周逐步将血糖调整到位的方法,观察治疗前后血糖、血浆C肽(C-P)空腹、餐后1小时、2小时及HbAlc的变化。结果两组的血糖及HbAlc较治疗前明显下降(P<0.05),而CSII组下降更为明显(P<0.05),且该组C-P空腹及餐后1小时值有所升高(P<0.05),胰岛素用量也较MSII组有所减少。结论对初诊的血糖较高的2型糖尿病患者尽早应用持续皮下胰岛素输注的方式,更有助于将血糖控制在理想水平及改善胰岛功能。 相似文献
2.
目的:观察膝关节骨性关节炎中老年患者通过太极拳运动结合肌肉锻炼,其关节功能及肌力的变化.方法:在成都市武侯区簇锦社区中选取100例中老年膝骨关节炎患者,按照随机、对照法分为运动疗法干预组(简称:干预组)和对照组,每组50例.对照组给予健康宣教及口服塞来昔布胶囊,干预组在对照组基础上增加运动疗法,持续4周.分别于干预前、... 相似文献
3.
肝细胞性肝癌中乙酰肝素酶与nm23-H1的表达及其临床意义 总被引:16,自引:0,他引:16
目的:探讨乙酰肝素酶(HPA)和nm23-H1在原发性肝细胞肝癌(HCC)中的相互关系,及其作为CC术后转移复发预测指标的价值。方法:选用33例HCC癌组织和癌旁组织标本,9例肝脏良性肿瘤瘤周肝组织作正常对照。用逆转录聚合酶链反应(RT-PCR)和免疫组化S-P法检测标本中HPA mRNA和nm23-H1蛋白的表达,并结合患者的临床病理指标和随访结果进行分析。结果:33例HCC中,16例HPA表达阳性,其阳性率显著高于癌旁组织和正常肝组织(P<0.01)。HPA表达与肿块大小、包膜形成、AFP水平、HBsAg状态和有无肝硬化等无关(P>0.05);但高转移复发倾向组和随访转移复发组HPA表达率显著高于低转移复发倾向组(P<0.05)和无转移复发组(P<0.01);此外,HPA基因表达多见于分化较差(P<0.05)、TNM分期较晚(P<0.05)的患者。nm23-H1蛋白在HCC癌组织中的阳性率显著低于癌旁和正常肝组织(P<0.05)。nm23-H1与肿块大小、包膜形成、AFP水平、HBsAg状态、有无肝硬化、Edmondson分级和TNM分期均无关(P>0.05);但高转移复发倾向组和随访转移复发组HPA表达率明显高于低转移复发倾向组(P=0.018)和无转移复发组(P=0.024)。nm23-H1在HPA阳性组和阴性组表达差异无显著意义(P=0.082)。按随访结果判断,HPA阳性预测转移复发准确率为78.6%(11/14);nm23-H1阴性预测准确率为68.8%(11/16);PHA阳性和nm23-H1阴性联合应用预测准确率为88.9%(8/9)。结论:HPA表达阳性和/或nm23-H1阴性患者有较高的肿瘤侵袭性和术后转移复发倾向,二者联合检测可提高预测HCC术后转移复发的准确性。 相似文献
4.
Yuan Guo Yi Liu Mingdong Guan Hongchi Tang Zilong Wang Lihua Lin Hao Pang 《RSC advances》2022,12(29):18848
Due to energy and environmental concerns, biobutanol is gaining increasing attention as an alternative renewable fuel owing to its desirable fuel properties. Biobutanol production from lignocellulosic biomass through acetone–butanol–ethanol (ABE) fermentation has gained much interest globally due to its sustainable supply and non-competitiveness with food, but large-scale fermentative production suffers from low product titres and poor selectivity. This review presents recent developments in lignocellulosic butanol production, including pretreatment and hydrolysis of hemicellulose and cellulose during ABE fermentation. Challenges are discussed, including low concentrations of fermentation sugars, inhibitors, detoxification, and carbon catabolite repression. Some key process improvements are also summarised to guide further research and development towards more profitable and commercially viable butanol fermentation.Due to energy and environmental concerns, biobutanol is gaining increasing attention as an alternative renewable fuel owing to its desirable fuel properties. 相似文献
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目的 利用信息化技术,在云南省边境地区建立持续动态症状监测预警系统,并探讨其有效性和及时性,以提升边境地区传染病防控能力。方法 选择3个边境县,以全覆盖的方式,于2016年1月至2018年2月持续监测医疗机构14个症状及6个症候群,收集小学每天学生缺勤信息和边境口岸入境人员发热信息,构建基于手机和电脑平台的症状监测预警系统。结果 采用EARS-3C和Kulldorff时空扫描的预警模型,发现皮疹、流感样症状和小学缺勤等多个监测信号源对手足口病、流感和水痘等常见传染病预警有较高的灵敏度和特异度(可提前1~5 d预警)。系统简便易用,安全性和可行性较强,以交互式图表及可视化地图的方式展示,相关人员能够随时掌握监测数据情况和预警信号的变化,及时采取处置措施。结论 该系统科学有效、操作方便,能实时发现边境地区常见传染病的暴发或聚集事件,实现及时采取有效干预措施,减少本地及跨境传染病暴发的风险,具有实际应用价值。 相似文献
8.
A radical trifluoromethylation reaction of tertiary enamides was investigated and trifluoromethyl-containing isoindolinones were prepared under mild conditions. Using TMSCF3 as a radical source, PhI(OAc)2 as an oxidant and KHF2 as an additive, tertiary enamides were converted to isoindolinones via a cascade addition and cyclization process in moderate to good yields.Radical trifluoromethylation and cyclization of tertiary enamides was developed and trifluoromethyl-containing isoindolinones were obtained in moderate to good yields.In recent years, trifluoromethyl-containing azaheterocycles have attracted much attention for their potential application in the fields of pharmaceutical and agricultural chemistry.1 Thus, lots of efforts have been devoted to the synthesis of trifluoromethyl azaheterocycles,2 and among these developed methods, radical cascade addition and cyclization has emerged as a remarkable strategy due to its unique properties such as economy and high efficiency. Unsaturated amides are commonly used substrates for this type of transformation, which could be attacked by a CF3 radical followed by intramolecular C–O, C–N, or C–C bond formation to give different kinds of trifluoromethyl azaheterocycles. Fu reported a metal-free trifluoromethylation of N-allyamides with CF3SO2Na for the synthesis of trifluoromethyl-containing oxazolines via oxytrifluoromethylation.3 In the presence of copper salts, N-acyl-2-allylaniline could be converted to trifluoromethylated indolines in moderate to good yields via aminotrifluoromethylation process.4 With Togni''s reagent,5 TMSCF3,6 CF3SO2Na,7 CF3SO2Cl8 and other reagents9 as the CF3 source, α, β-unsaturated amides, tosyl amides, or imides underwent a tandem conversion to give trifluoromethyl-containing oxindoles or isoquinoline-1,3-diones by trifluoromethylation/arylation reaction. On the other hand, as a special type of unsaturated amide containing an active double bond, enamide also exhibited excellent reactivity in radical reactions.10 In fact, trifluoromethylation of enamides has already been investigated, and in most cases trifluoromethylated alkenes were obtained as the main products.11 To the best of our knowledge, the radical trifluoromethylation and cyclization of enamide still remains undeveloped.Isoindolinones are important N-heterocyclic compounds necessary in organic and pharmaceutical chemistry, and these compounds are used widely as anticoagulants and tranquilizers such as aristolactam, pagoclone, and zopiclone.12 To introduce a CF3 group into isoindolinones, Wang and co-workers explored a convenient way to the synthesis of trifluoromethyl-containing isoindolinones by radical aminotrifluoromethylation (Scheme 1a),13 but this transformation only occurred for N-methoxylbenzamides, and in case of N-alkylbenzamides trifluoromethylated alkenes were obtained as the major products. 1,1-disubstituted terminal alkenes were also not suitable substrates because of the competition between O-trapping and N-trapping process. Thus, development a new method for the synthesis of trifluoromethyl-containing isoindolinones is still in demand. Here in, as a continuation of our efforts on the radical modification of amide derivatives,14 we wish to present our work on the synthesis of trifluoromethyl-containing isoindolinones using enamides as the start materials by radical carbon trifluoromethylation (Scheme 1b).Open in a separate windowScheme 1Synthesis of trifluoromethyl-containing isoindolinones.Initially, N-n-butyl-N-(2-propenyl) benzamide 1a was chosen as the model substrate to optimize the reaction conditions of this radical carbontrifluoromethylation process. As shown in Entry Additive (0.3 equiv.) Solvent (2 mL) Temp. (°C) Yield of 2ab (%) 1 NaF EtOAc 80 15 2 KF EtOAc 80 38 3 CsF EtOAc 80 35 4 NaHF2 EtOAc 80 52 5 KHF2 EtOAc 80 75 6 NH5F2 EtOAc 80 40 7 KHF2 CH3CN 80 21 8 KHF2 CH2Cl2 80 32 9 KHF2 Toluene 80 Trace 10 KHF2 EtOAc 100 61 11 KHF2 EtOAc 60 43 12 KHF2 EtOAc r.t. NR 13 KHF2 EtOAc 80 37c 14 KHF2 EtOAc 80 62d 15 KHF2 EtOAc 80 58e, 47f 16 KHF2 EtOAc 80 73g