全文获取类型
收费全文 | 38658篇 |
免费 | 3121篇 |
国内免费 | 1001篇 |
专业分类
耳鼻咽喉 | 202篇 |
儿科学 | 641篇 |
妇产科学 | 550篇 |
基础医学 | 2013篇 |
口腔科学 | 256篇 |
临床医学 | 3857篇 |
内科学 | 5817篇 |
皮肤病学 | 339篇 |
神经病学 | 3020篇 |
特种医学 | 1004篇 |
外国民族医学 | 1篇 |
外科学 | 2788篇 |
综合类 | 4217篇 |
现状与发展 | 1篇 |
一般理论 | 3篇 |
预防医学 | 3992篇 |
眼科学 | 203篇 |
药学 | 11163篇 |
15篇 | |
中国医学 | 1606篇 |
肿瘤学 | 1092篇 |
出版年
2024年 | 69篇 |
2023年 | 715篇 |
2022年 | 867篇 |
2021年 | 1551篇 |
2020年 | 1465篇 |
2019年 | 1455篇 |
2018年 | 1447篇 |
2017年 | 1481篇 |
2016年 | 1405篇 |
2015年 | 1374篇 |
2014年 | 2885篇 |
2013年 | 3723篇 |
2012年 | 2400篇 |
2011年 | 2518篇 |
2010年 | 1944篇 |
2009年 | 1721篇 |
2008年 | 1673篇 |
2007年 | 1664篇 |
2006年 | 1439篇 |
2005年 | 1246篇 |
2004年 | 1057篇 |
2003年 | 982篇 |
2002年 | 695篇 |
2001年 | 670篇 |
2000年 | 581篇 |
1999年 | 493篇 |
1998年 | 513篇 |
1997年 | 437篇 |
1996年 | 409篇 |
1995年 | 442篇 |
1994年 | 307篇 |
1993年 | 316篇 |
1992年 | 316篇 |
1991年 | 272篇 |
1990年 | 245篇 |
1989年 | 194篇 |
1988年 | 219篇 |
1987年 | 152篇 |
1986年 | 163篇 |
1985年 | 209篇 |
1984年 | 179篇 |
1983年 | 122篇 |
1982年 | 127篇 |
1981年 | 88篇 |
1980年 | 102篇 |
1979年 | 78篇 |
1978年 | 85篇 |
1977年 | 73篇 |
1976年 | 53篇 |
1975年 | 53篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
61.
Dr. B. H.Ch. Stricker R. R. M. de Groot J. H. P. Wilson 《European journal of clinical pharmacology》1991,40(4):367-371
Summary In 1981 generalized anaphylaxis was registered on 166 occasions in Dutch general and academic hospitals. Clinical details of 120 of those patients revealed that in 107 anaphylaxis was either probable (n=90) or possible (n=17), whereas in 13 cases some other reaction than anaphylaxis had occurred. The series of confirmed cases contained 46 men and 61 women, with mean ages of 47 y and 48 y, respectively.There was a complete recovery in 102 patients and two patients died. Hypotension was present in 79 cases (74%), dyspnoea in 34 cases (32%) and a skin reaction, mainly urticaria, erythema or angioedema, was mentioned in 62 cases (58%). Most cases of anaphylaxis were drug-induced (76%), the main causes being the analgesic glafenine and contrast media. Glafenine was mentioned as the cause in 36% of all admissions for drug-induced anaphylaxis. Only 3.7% of cases had been reported to the voluntary reporting scheme of the Netherlands Centre for Monitoring of Adverse Reactions to Drugs.On the basis of reimbursement data, the risk of developing severe anaphylaxis to glafenine was estimated at 11.7–19.3-fold relative to indomethacin, and 13.4–20.2-fold relative to oral penicillins. 相似文献
62.
The toxic effects of nitroquine-dapsone compound(NQD)in mice and dogs were studied.The therapeutic index of NQDin mice is 1911,the greatest among the 6 antimalarials tested.Thetoxic effects of NQD(50 mg/kg/day for 3 days per os)and nitro-quine in dogs were manifested by injuries on the adrenal cortexand intestinal epithelium.When folic acid(4 mg/kg/day for 4 days)or calcium leucovorinum(0.3 mg/kg/day for 4 days)were usedconcomitantly with NQD,the death rate and the incidence of dia-rrhea in the toxicated dogs were greatly reduced,the injury on theintestinal epithelium was much milder,and the goblet cells weremuch more numerous than those without treatment.The results suggestthat folic acid and calcium leucovorinum can protect the undifferen-tiated cells in the intestinal crypts from being injured by NQD. 相似文献
63.
Detection of Atrial Fibrillation by Implanted Devices with Wireless Data Transmission Capability 总被引:3,自引:0,他引:3
NIRAJ VARMA† BRUCE STAMBLER SUNG CHUN† 《Pacing and clinical electrophysiology : PACE》2005,28(S1):S133-S136
Remote telemetry may facilitate the management of implantable devices. We tested the reliability of a new automatic, wireless home monitoring (HM) system that archives data every 24 hours. We retrospectively analyzed archival data from 276 consecutive pacing system implants to define temporal atrial fibrillation (AF) patterns and associated ventricular rate. An "AF day" was defined by a >20%/24 hour mode switch (MS) duration, irrespective of the MS number. Management decisions resulting from transmissions were noted. A pilot study confirmed that 89% of 22,356 transmissions were successful, of which >90% were received in <5 minutes. Data integrity was 100% preserved. Overall, AF developed in 29 patients (10.5%), representing a total of 645 AF days (mean = 22.2 ± 29.6 AF, median = 9 days), over 12 ± 2 months of monitoring. AF was infrequent (50% of 24 hours. Ventricular rates during 645 AF days in 29 patients averaged 95.1 ± 9.9 beats/min (median = 94 beats/min). Ventricular rates were >80 beats/min in 25 ± 30 AF days (median = 11 days). HM enabled rapid anticoagulation decisions. In recipients of implantable devices, automatic wireless telemetry with HM was efficient and reliable. Its application may overcome some current challenges in AF management by early notification and precise measurement of both AF burden and ventricular rate during AF. 相似文献
64.
Y. Le Meur M. Büchler A. Thierry S. Caillard F. Villemain S. Lavaud I. Etienne P.-F. Westeel B. H. de Ligny L. Rostaing E. Thervet J. C. Szelag J.-P. Rérolle A. Rousseau G. Touchard P. Marquet 《American journal of transplantation》2007,7(11):2496-2503
Efficacy and safety of mycophenolate mofetil (MMF) may be optimized with individualized doses based on therapeutic monitoring of its active metabolite, mycophenolic acid (MPA). In this 12-month study, 137 renal allograft recipients from 11 French centers receiving basiliximab, cyclosporine A, MMF and corticosteroids were randomized to receive either concentration-controlled doses or fixed-dose MMF. A novel Bayesian estimator of MPA AUC based on three-point sampling was used to individualize doses on posttransplant days 7 and 14 and months 1, 3 and 6. The primary endpoint was treatment failure (death, graft loss, acute rejection and MMF discontinuation). Data from 65 patients/group were analyzed. At month 12, the concentration-controlled group had fewer treatment failures (p = 0.03) and acute rejection episodes (p = 0.01) with no differences in adverse event frequency. The MMF dose was higher in the concentration-controlled group at day 14 (p < 0.0001), month 1 (p < 0.0001) and month 3 (p < 0.01), as were median AUCs on day 14 (33.7 vs. 27.1 mg*h/L; p = 0.0001) and at month 1 (45.0 vs. 30.9 mg*h/L; p < 0.0001). Therapeutic MPA monitoring using a limited sampling strategy can reduce the risk of treatment failure and acute rejection in renal allograft recipients 12 months posttransplant with no increase in adverse events. 相似文献
65.
目的 探讨实验性内听动脉阻断与术后听力改变的关系及术中听觉监控的方法。方法 实验兔乙状窦后进路暴露小脑桥脑角,下压小脑暴露内听道及第Ⅷ神经复合体,分辨出内听动脉,予阻断不同时间,分别行蜗神经直接复合动作电位(DCAP)和畸变产物耳声发射记录(DPOAE)。结果对照组DCAPN1波潜伏期值无明显改变。内耳血供阻断10s和30s组在压迫开始后3min,DCAPN1波潜伏期值均恢复为初始值。内耳血供阻断1min组在压迫开始后3h,DCAPN1波潜伏期值未恢复为初始值假手术组DPOAE幅值无明显改变,内耳血供阻断10s、30s对DPOAE幅值无影响,内耳血供阻断1min使得DPOAE幅值下降结论兔内耳血供阻断1min可能造成兔听觉不可逆损伤。DCAP、DPOAE能有效、持续地监控内耳血供阻断,是耳神经外科手术中实用的听觉监测手段。 相似文献
66.
早期脑室置管行颅内压监护对中型颅脑损伤患者的预后影响 总被引:1,自引:0,他引:1
目的 探讨早期脑室置管行颅内压 (ICP)和脑灌注压 (CPP)监护在中型颅脑损伤中的临床应用价值。方法 将 12 5例伤后 2 4h入院无手术指征的中型颅脑损伤 (GCS 9~ 12分 )患者 ,随机分为ICP监护组 :入院后即经恻脑室内穿刺置管行ICP与CPP连续监测 ,根据颅内压变化调整治疗方案 ;对照组 :入院后不做ICP监测 ,依据临床观察的意识及生命体征变化 ,进行治疗。结果 颅内压监护组脱水剂剂量、应用时间均低于对照组 ,疗效优于对照组 ,两组差异有显著意义 (P <0 0 5 )。结论 中型颅脑损伤病情极不稳定 ,早期行ICP监护能及早发现病情变化 ,对及时采取有效治疗措施 ,降低死残率 ,改善预后有重要意义。 相似文献
67.
中药血清化学是在传统的口服给药模式的基础上,依据中药口服后只有移行入血的成分才可能发挥药效的思路,通过综合运用现代的提取、分析技术,对药物口服吸收后含药血清中的原型药物及其代谢产物进行分析研究,从而可直接筛选和判断出中药及复方中的有效成分并据此较快速地探明其药效物质基础,同时辅助阐明中药复方的配伍机制和意义,对中药新药的研发起到加速和推动作用。文中作者总结了一些血清药物化学的成功实践经验,并对血清药物化学的研究方法进行了归纳和概述。 相似文献
68.
Bernard Farrell 《Journal of diabetes science and technology》2007,1(2):245-250
The continuous glucose monitor market is just starting to develop. Current trends in the availability of diabetes information tools highlight the need for standard data presentation for continuous glucose monitors. These trends and their implications are discussed. This article proposes a set of standards for blood glucose data presentation. If device manufacturers adopt these standards, they will ensure that their continuous glucose monitors meet both the short-term and the long-term needs of users. This should increase the demand for these monitors and enable future device developments that appeal to a wider range of users. 相似文献
69.
厄贝沙坦治疗高血压患者的临床效果观察 总被引:1,自引:0,他引:1
目的:观察厄贝沙坦治疗高血压患者的临床效果。方法:选择2007年1月~2009年1月来本院就诊的高血压患者200例,随机分为两组,厄贝沙坦组100例,采用厄贝沙坦治疗4周;对照组100例采用依那普利治疗,观察患者用药前后动态血压、心脏功能变化,并评价临床疗效。结果:厄贝沙坦组患者治疗总有效率为97%,均未出现明显不良反应:与对照组比较.差异有统计学意义,P〈0.05。厄贝沙坦组治疗后24h、白昼和夜间平均收缩压和舒张压与治疗前比较,差异有统计学意义,P〈0.05;用药后血压晨峰也显著降低,与治疗前比较,差异有统计学意义,P〈0.05:但与对照组间比较,差异无统计学意义,P〉0.05。结论:厄贝沙坦治疗高血压疗效满意,安全性较高,还可降低患者的心脑血管意外的风险。 相似文献
70.