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81.
目的:观察左布匹卡因与罗比卡因用于腹部手术后自控硬膜外镇痛(PCEA)的效果及不良反应。方法:60例ASAⅠ~Ⅱ级腹部手术患者,随机分为0.15%左布匹卡因加2mg/L芬太尼组(A组)30例与0.2%罗比卡因加2mg/L芬太尼组(B组)30例,以5mL/h行术后硬膜外泵注镇痛。记录术后4、8、24、48h的疼痛视觉模拟评分(VAS0~10分)、满意度评分、运动阻滞测试(改良Bromage评分)及术后活动能力4级评分;48h内按压PCA次数(PCAd)、PCA有效次数(PCAe)、D/D比值(PCAd/PCAe)及不良反应。结果:2组镇痛效果满意,2组各观察指标差别均无统计学意义(P〉0.05)。在术后第1天。A组有14例(46.7%)可以短时间行走,而B组有25例(83.3%)。第2天,A组有15例(50.0%)可以自由行走,而B组有26例(86.7%),2组差别有统计学意义(P〈0.05)。不良反应:恶心发生率A组13.3%(4/30),B组10.0%(3/30)。皮肤瘙痒发生率2组均为6.7%(2/30),差异无统计学意义(P〉0.05)。结论:0.15%左布匹卡因与0.2%罗比卡因用于患者术后硬膜外镇痛均可获得满意的效果,而0.2%罗比卡因较0.15%左布匹卡因术后活动能力恢复早。 相似文献
82.
83.
Zhou TJ Chiu JW White PF Forestner JE Murphy MT 《Acta anaesthesiologica Scandinavica》2001,45(2):246-249
BACKGROUND: The use of volatile anesthetics for maintenance of anesthesia can enhance the action of non-depolarizing muscle relaxants and interfere with the reversal of neuromuscular blockade. In this study, we studied the antagonism of rocuronium with edrophonium-atropine during propofol- versus sevoflurane-based anesthesia. METHODS: Following induction of anesthesia with propofol (2-2.5 mg kg(-1), i.v.) and fentanyl (1-2 microg kg(-1) i.v.), rocuronium 0.6 mg kg(-1) i.v. was administered to facilitate tracheal intubation. Patients were then randomized to receive either a propofol infusion (100 microg kg(-1) min(-1)) or sevoflurane (1.0%, end-tidal) in combination with nitrous oxide 66% for maintenance of anesthesia. Neuromuscular blockade was monitored using electromyography at the wrist, and reversed with edrophonium 1.0 mg kg(-1) and atropine 0.015 mg kg(-1) when the first twitch hight (T1) of the train-of-four (TOF) stimulation recovered to 25% of the baseline value. Anesthetic maintenance with propofol or sevoflurane was continued following reversal until a TOF ratio of 0.7 was attained. RESULTS: The clinical duration of action (i.e., time to 25% T1 recovery) was similar during both propofol- (39.3+/-14.6 min) and sevoflurane-based (48.1+/-19.7 min) anesthesia. However, the reversal time from 25% T1 to TOF ratio of 0.7 was significantly longer with sevoflurane [Median 2.8 (range 0.5-18.8) min] compared with propofol [1.5 (0.75-3) min] (P<0.05). CONCLUSIONS: We conclude that the clinical duration of action after a single dose of rocuronium, 0.6 mg kg(-1) i.v., was similar during both propofol- and sevoflurane-based anesthesia. However, the reversal of rocuronium-induced residual blockade was slower and more variable in the presence of sevoflurane. 相似文献
84.
The influence of halothane, isoflurane and sevoflurane on rocuronium infusion in children 总被引:2,自引:0,他引:2
Woloszczuk-Gebicka B Lapczynski T Wierzejski W 《Acta anaesthesiologica Scandinavica》2001,45(1):73-77
BACKGROUND: Rocuronium is a non-depolarizing neuromuscular blocking agent with intermediate duration of action and without significant cumulative properties, suitable for continuous infusion. This study was designed to determine the infusion requirements in children under nitrous oxide and fentanyl, halothane, isoflurane or sevoflurane anaesthesia. METHODS: Forty children, 3-11 years old, ASA physical status group I or II were studied. They were randomly allocated to receive fentanyl-nitrous oxide, 1 MAC halothane-nitrous oxide, 1 MAC isoflurane-nitrous oxide or 1 MAC sevoflurane-nitrous oxide anaesthesia. Rocuronium, 0.6 mg(-1) was used to facilitate endotracheal intubation. Electromyographic response of adductor pollicis to train-of-four (TOF) stimulation, 2 Hz for 2 s, applied to the ulnar nerve at 10-s intervals was recorded using Relaxograph (Datex, Helsinki, Finland). Once the first twitch response (T1) returned to 5%, muscle relaxation was maintained by continuous infusion of rocuronium, adjusted automatically in a closed-loop system to maintain a stable 90-99% T1 depression. The block was considered stable if it changed by no more than 2% over a 10-min observation period. RESULTS: Halothane, isoflurane and sevoflurane groups had ower infusion requirements than the fentanyl-nitrous oxide group (P<0.00075). Rocuronium requirement (mean +/- SD) at one hour from the commencement of anaesthesia was 16.7+/-2.3, 13.6+/-3.7, 13.1+/-5.1 and 8.4+/-1.6 microg x kg(-1) x min(-1) for children receiving fentanyl-nitrous oxide, halothane, isoflurane and sevoflurane anaesthesia, respectively. CONCLUSIONS: The rocuronium infusion rate required to maintain stable 90-99% T1 depression was reduced by approximately 20% with halothane and isoflurane anaesthesia, and by 50% with evoflurane anaesthesia when compared to fentanyl-nitrous oxide anaesthesia. Significant patient-to-patient variability of infusion rate makes monitoring of neuromuscular transmission necessary. 相似文献
85.
The stability of submicron emulsions of different local anesthetic/analgesic substances was investigated in the presence and absence of different hydrophobic excipients (ripening inhibitors). Ostwald ripening was believed to be the underlying mechanism for the instability of these emulsions. In the absence of ripening inhibitors, the mean droplet size of the emulsions increased from 100 nm to about 4–5 μm within an hour of manufacture. The addition of a small amount of a second component of lower solubility to the disperse phase decreased the rate of Ostwald ripening, producing good stability of the emulsions. The efficiency of the ripening inhibitors was directly proportional to their solubility in the disperse phase, i.e. the water. The lower the solubility, the more effective the stabilization of the emulsions. The experimentally observed rates of increase in droplet size in the emulsions were closely correlated with those predicted according to the Liftshitz–Slezov–Wagner (LSW) theory. 相似文献
86.
Tatsuya Yamada MD Junzo Takeda MD Kaoru Koyama MD Hiromasa Sekiguchi MD Kazuaki Fukushima MD Taro Kawazoe MD 《Journal of cardiothoracic and vascular anesthesia》1994,8(6)
The effects of volatile anesthetics on active (ventricular relaxation) and passive (chamber stiffness) indices of diastolic function and on left ventricular filling rates in dogs were studied to determine how these agents affect left ventricular diastolic performance. Thirty-five mongrel dogs were randomly assigned to receive sevoflurane, isoflurane, enflurane, or halothane. Left ventricular pressure waveforms, phonocardiograms, and echocardiograms were recorded after administering the anesthetics at concentrations of 0% (control), 1%, 2%, and 3%. Ventricular relaxation was defined as the time constant of the decline in left ventricular pressure. Chamber stiffness was derived from the ventricular pressure-volume relationship during passive filling. Rapid filling rate, slow filling rate, and atrial filling rate were obtained from echocardiograms and phonocardiograms. No change in the time constant or in chamber stiffness was observed at any concentration of sevoflurane or isoflurane. However, the highest studied concentration of enflurane and halothane produced a significant increase in the time constant and in chamber stiffness. Rapid filling rate as well as atrial filling rate decreased significantly with the volatile anesthetics, especially with enflurane and halothane. Sevoflurane and isoflurane did not alter ventricular relaxation or chamber stiffness, but did affect diastolic function as manifested by their alteration of filling rates. In contrast, enflurane and halothane each prolonged ventricular relaxation and increased chamber stiffness. With the administration of the volatile anesthetics, the rapid filling rate decreased with the deterioration of diastolic function; in addition, atrial filling rates decreased and did not compensate for the reduction in early ventricular filling. 相似文献
87.
The subcutaneous absorption kinetics of a homologous series of local anesthetics and lidocaine were studied under controlled pH conditions using a previously described in vivorat model. All local anesthetics exhibited biexponential absorption profiles suggesting accumulation into a tissue compartment. Evidence supporting this hypothesis was supplied by back-extraction of lidocaine from subcutaneous tissue into an acidic environment, by multiple dosing experiments, and by movement of compound into subcutaneous tissue of a postmortem rat preparation. A series of interanimal relationships were demonstrated between structure and parameters of a twocompartment open model. Particularly striking were the correlations between in vivopartition and tissue clearance and the octanolwater (pH 7.95)partition coefficients.Supported by National Institutes of Health Training Grant No. 5T01 GM 00728 from the National Institute of General Medical Sciences and by research funds from the Academic Senate Committee on Research, University of California at San Francisco.Abstracted in part from a thesis submitted by René H. Levy to the Graduate Division, University of California at San Francisco, in partial fulfillment of the Doctor of Philosophy degree requirements.This paper was submitted to a Consulting Editor who served as the Journal Editor during its review process. 相似文献
88.
In this article we review how population pharmacokinetic/pharmacodynamic (PD) modeling has evolved in the specialty of anesthesiology, how anesthesiology benefited from the mixed-effects approach, and which features of modeling need careful attention. Key articles from the anesthesiology literature are selected to discuss the modeling of typical anesthesiological PD end points, such as level of consciousness and analgesia, interactions between hypnotics and analgesics, estimation with poor and sometimes rich data sets from populations of various sizes, covariate detection, covariances between random effects, and Bayesian forecasting. 相似文献
89.
Suliburk JW Gonzalez EA Moore-Olufemi SD Weisbrodt N Moore FA Mercer DW 《The Journal of surgical research》2005,127(2):203-207
INTRODUCTION: Lipopolysacharide (LPS) causes gastrointestinal ileus and gastric luminal fluid accumulation. Ketamine, an anti-inflammatory anesthetic agent attenuates accumulation of luminal fluid. However, its effects on gastrointestinal transit induced by endotoxemia are unknown. The purpose of this study was to determine if the anti-inflammatory properties of ketamine improve impaired gastric emptying and gastrointestinal transit because of LPS. MATERIALS AND METHODS: Rats were given ketamine (70 mg/kg i.p.) or saline 1 h before LPS (20 mg/kg, i.p.) or saline injection. Five hours after LPS injection, rats were gavaged with 1 cc consisting of 0.1 ml of 5 mm FITC Dextran added to 0.9 ml of saline. After 30 min, rats were sacrificed, and gastric emptying, gastrointestinal transit, and gastric fluid accumulation determined. Gastric and ileal mucosa were harvested for analysis of inducible nitric oxide synthase (iNOS) (Western immunoblot). Results are reported as mean +/- SE (n > or = 5 per group; ANOVA). RESULTS: Ketamine did not prevent LPS induced gastrointestinal ileus, nor did it improve gastric emptying. More importantly, it did not worsen gastrointestinal function or gastric emptying when compared to saline controls. However, it did decrease LPS induced gastric luminal fluid accumulation and blunted iNOS expression in both the stomach and ileum. CONCLUSION: These data indicate that the ability of ketamine to attenuate gastric fluid accumulation is not because of improved gastric emptying or improved gastrointestinal transit. Moreover, while iNOS may play a role in LPS induced gastric luminal fluid accumulation, it does not appear to be a major mediator of the gastrointestinal ileus caused by LPS. 相似文献
90.
A study was performed in which both anterograde ([3H]leucine radioautography) and retrograde (horseradish peroxidase (HRP) histochemistry) tracing methods were employed to identify the origin of the fimbrial projection to the nucleus accumbens in the rat. The data reveal that this pathway arises predominantly from layers II–III of the anterior two-thirds of entorhinal cortex rather than from any part of hippocampal formation. 相似文献