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91.
腹腔镜手术病人咪达唑仑-芬太尼-异丙酚麻醉诱导的优化配伍方案 总被引:3,自引:0,他引:3
目的 采用权重配方法探讨腹腔镜手术病人咪达唑仑、芬太尼、异丙酚复合麻醉诱导的优化配伍方案。方法选择ASAⅠ或Ⅱ级择期腹腔镜手术病人60例,男34例,女26例,年龄31~55岁。诱导药物的低效量和足量分别确定为咪达唑仑0.02、0.06mg/kg,芬太尼2、6μg/kg,异丙酚0.5、1.5mg/kg。根据权重配方法,将病人随机分配至3种药物不同剂量组合的6个配伍组(n=10)。连续监测脑电双频谱指数(BIS)、心率(HR)、平均动脉压(MAP)、脉搏血氧饱和度(SpO2)。各组依次静脉注射相应剂量咪达唑仑、芬太尼、异丙酚和罗库溴铵0.6mg/kg行麻醉诱导和气管插管。记录诱导前即刻、异丙酚注入后1、2min、插管即刻、插管后1、3、5、7min的BIS、MAP及HR。按权重配方法的剂量优化原则评判复合药效,分析各组份药的重要程度及相互作用的性质。结果以BIS为评价指标,当咪达唑仑0.06mg/kg、芬太尼5μg/ks、异丙酚1.0mg/kg配伍时,异丙酚为主药,异丙酚与咪达唑仑和芬太。尼具有相加性作用;以MAP为评价指标,当咪达唑仑0.06mg/kg、芬太尼5μg,kg、异丙酚1.5mg/kg配伍时,异丙酚为主药,异丙酚与咪达唑仑具有协同性作用,异丙酚与芬太尼具有相加性作用;以HR为评价指标,当咪达唑仑0.06mg/kg、芬太尼5μg/kg、异丙酚1.0mg/kg配伍时,芬太尼为主药,异丙酚与咪达唑仑和芬太尼具有协同性作用。结论腹腔镜手术病人咪达唑仑、芬太尼、异丙酚复合麻醉诱导在维持镇静方面为相加作用,在维持血液动力学稳定方面为协同作用;优化配伍方案为咪达唑仑0.06mg/kg、芬太尼5μg/kg、异丙酚1.5mg/kg。 相似文献
92.
控制性降压在鼻内窥镜手术中的应用 总被引:2,自引:0,他引:2
目的 :观察控制性降压在鼻内窥镜手术中应用的意义。方法 :80例双侧鼻息肉、鼻窦炎患者 ,局麻、鼻内窥镜下行双侧鼻息肉摘除、全筛切除及开放上颌窦自然开口。其中 38例术中控制性降压 (降压组 ) ,另 42例作为对照。结果 :降压组术中出血 (6 1 39± 38 5 2 )ml,对照组出血 (140 12± 81 82 )ml,差异有显著性意义 (P <0 0 1) ;手术时间分别为 (4 9 2 5± 7 0 6 )min和(6 2 4 0± 9 90 )min ,差异有显著性意义 (P <0 0 1)。结论 :控制性降压可明显减少术中出血 ,缩短手术时间。 相似文献
93.
Transfer of clonidine and dexmedetomidine across the isolated perfused human placenta 总被引:4,自引:0,他引:4
T. I. ALA-KOKKO P. PIENIMÄKI E. LAMPELA A. I. HOLLMÉN O. PELKONEN K. VÄHÄKANGAS 《Acta anaesthesiologica Scandinavica》1997,41(2):313-319
Background: The placental transfer of the a2 receptor agonist clonidine, earlier used as an adjuvant in obstetric epidural analgesia, was compared with the transfer of the newer and more %-selective agonist dexmedetomidine.
Methods: Term placentas were obtained immediately after delivery with maternal consent and a 2-hour recycling perfusion of a single placental cotyledon was performed. Disappearance from the maternal circulation, accumulation in placental tissue and appearance in the fetal circulation of clonidine or dexmedetomidine with the reference compound antipyrine were followed in 4 experiments for both drugs.
Results: At 2 hours the percent dexmedetomidine found in the fetal circulation was 12.5 (SD 5.1)%, while 48.1 (SD 20.3)% was found in the perfused placental cotyledon. A higher mean clonidine than dexmedetomidine concentration was achieved in the fetal circulation (1.90 vs. 0.56 nmol/l, P <0.05). At 2 hours the percent clonidine found in the fetal circulation was 22.1 (SD 2.4)% ( P <0.05), while 11.3 (SD 3.3)% ( P <0.05) was re tained in the perfused placental cotyledon. The transfer indexes, describing maternal-to-fetal transfer of dexmedetomidine and clonidine normalized with the transfer of antipyrine, were 0.88 (SD 0.07) and 1.04 (SD 0.08) respectively ( P <0.05).
Conclusions: Dexmedetomidine disappeared faster than clonidine from the maternal circulation, while even less dexmedetomidine was transported into the fetal circulation. This was due to its greater placental tissue retention, the basis for which probably is the higher lipophilicity of dexmedetomidine. 相似文献
Methods: Term placentas were obtained immediately after delivery with maternal consent and a 2-hour recycling perfusion of a single placental cotyledon was performed. Disappearance from the maternal circulation, accumulation in placental tissue and appearance in the fetal circulation of clonidine or dexmedetomidine with the reference compound antipyrine were followed in 4 experiments for both drugs.
Results: At 2 hours the percent dexmedetomidine found in the fetal circulation was 12.5 (SD 5.1)%, while 48.1 (SD 20.3)% was found in the perfused placental cotyledon. A higher mean clonidine than dexmedetomidine concentration was achieved in the fetal circulation (1.90 vs. 0.56 nmol/l, P <0.05). At 2 hours the percent clonidine found in the fetal circulation was 22.1 (SD 2.4)% ( P <0.05), while 11.3 (SD 3.3)% ( P <0.05) was re tained in the perfused placental cotyledon. The transfer indexes, describing maternal-to-fetal transfer of dexmedetomidine and clonidine normalized with the transfer of antipyrine, were 0.88 (SD 0.07) and 1.04 (SD 0.08) respectively ( P <0.05).
Conclusions: Dexmedetomidine disappeared faster than clonidine from the maternal circulation, while even less dexmedetomidine was transported into the fetal circulation. This was due to its greater placental tissue retention, the basis for which probably is the higher lipophilicity of dexmedetomidine. 相似文献
94.
S. EINARSSON A. CERNE A. BENGTSSON O. STENQVIST J. P. BENGTSON 《Acta anaesthesiologica Scandinavica》1997,41(10):1285-1291
Background : The appearance of hypoxaemia immediately after anaesthesia with nitrous oxide may be partially explained by diffusion hypoxia. This study was undertaken to evaluate circulatory and respiratory variables during emergence after desflurane/nitrous oxide anaesthesia, and whether there are any differences depending on which gas is discontinued first. Methods : 20 patients were studied after gynaecological laparoscopic surgery. The depth of anaesthesia was reduced 10 min prior to the emergence by stopping the administration of one of the two inhalational agents. Desflurane was discontinued first in Group 1, nitrous oxide in Group 2. Ventilation was controlled with E'C02 maintained at 5% until the administration of the second anaesthetic gas was discontinued. Thereafter, the patients breathed spontaneously. Results : The PaC02 at which the respiratory drive reappeared after controlled normoventilation was similar in both groups, 6.1–6.5 kPa, and extubation was performed after 10–11 min. At extubarion, the end–tidal C02 and total MAC were similar in the groups, about 6.2 vol% and 0.16, respectively. Mean arterial blood pressure was significantly higher in Group 1. The cardiac output increased in both groups from about 6 1/min at the conclusion of anaesthesia to 9.0 and 7.6 1/min at 15 min in the recovery period. End–tidal O2 decreased and CO2 increased in both groups during the first 10 min in the recovery period. pH was reduced at 15 and 30 min in both groups. Conclusion : Irrespective of which agent was discontinued first, there was an increase in cardiac output, decrease in oxygenation and a modest acidosis in the first 30–min recovery period. The only significant difference between the groups was in mean arterial blood pressure in the early emergence phase with a greater MAP when N2O had been used until the conclusion of anaesthesia. 相似文献
95.
V. UMBRAIN J. D'HAESE M. ALAFANDY E. DE ROOVER A. SCHOUTENS B. VAN GANSBEKE A. ALBERT G. GOFFINET F. CAMU F. J. LEGROS 《Acta anaesthesiologica Scandinavica》1997,41(1):25-34
Background: Liposomes containing local anaesthetics have been administered intrathecally and in the epidural space. Poor attention has been given to the pharmacokinetics of liposomes as drug carriers. Therefore, we observed the biodistribution of liposomes after intrathecal injection in rats by scintigraphic imaging during 24 h.
Methods: We administered99 Tc-labeled multilamellar (MLV) and small unilamellar vesicles (SUV) of defined size and volume dispersities into the cerebrospinal fluid at the lumbar level. Those vesicles were free of contamination by radiolabeled colloids as visualized by light and electron microscopy and of neurotoxic products from phosphatidylcholine hydrolysis and peroxidation, both during the preparation process and after 24 h incubation in cerebrospinal fluid at 37°C in vitro.
Results: SUV immediately diffused from the lumbar site of injection to the head and were cleared between 1 and 24 h after injection. MLV were cleared more slowly from the spinal space and appeared in the head region 1 h after injection where they accumulated up to 24 h. These differences were explained in terms of vesicle sizes and volumes. SUV with 0.05 μm diameters were rapidly absorbed into the blood through the arachnoid granulations. In contrast, particles larger than the upper size limit of the arachnoid granulations permeability (±8 μm) could accumulate in the head with a slow elimination rate.
Conclusion: This difference in clearance from the intrathecal space outlines the importance of defining the size of the liposomes, the distribution of a tracer or a drug inside the liposomal preparation, the chemical stability and the absence of toxic degradation products of liposome formulations before clinical use. 相似文献
Methods: We administered
Results: SUV immediately diffused from the lumbar site of injection to the head and were cleared between 1 and 24 h after injection. MLV were cleared more slowly from the spinal space and appeared in the head region 1 h after injection where they accumulated up to 24 h. These differences were explained in terms of vesicle sizes and volumes. SUV with 0.05 μm diameters were rapidly absorbed into the blood through the arachnoid granulations. In contrast, particles larger than the upper size limit of the arachnoid granulations permeability (±8 μm) could accumulate in the head with a slow elimination rate.
Conclusion: This difference in clearance from the intrathecal space outlines the importance of defining the size of the liposomes, the distribution of a tracer or a drug inside the liposomal preparation, the chemical stability and the absence of toxic degradation products of liposome formulations before clinical use. 相似文献
96.
使用低流量循环密闭回路内注入给药法,比较1MAC代氟醚和安氟醚各14例维持全麻时循环动力苏醒情况和不良反应。结果;代氟醚在维持阶段对心血管系统的抑制较安氟醚为轻,很可能和代氟醚能使交感神经兴奋性增加有关。 相似文献
97.
This case report describes the anaesthetic management of a patient with sporadic-type long QT interval syndrome (LQTS), and increased QT dispersion, who presented for removal of an ovarian cyst. Beta adrenergic blockade and adequate depth of anaesthesia for successful management is emphasized. The Successful use of epidural administration of lignocaine and opioids in addition to general anaesthesia is described. 相似文献
98.
我们对50例子宫、卵巢手术病人,使用利多卡因做硬膜外麻醉,其中25例向硬膜外腔内注入异氟醚-氧化亚氮气体。2组对比发现,实验组麻醉平面明显高于对照组,在同样手术时间内实验组所使用的利多卡因量明显少于对照组。表明异氟醚-氧化亚氮气体有增强利多卡因的硬膜外麻醉作用,同时未发现注入吸入麻醉药产生副作用。 相似文献
99.
硬膜外腔阻滞对胸部手术应激反应的影响 总被引:33,自引:1,他引:32
目的 观察硬膜外腔阻滞对胸部手术应激激素和细胞因子的影响。方法20例食管癌手术病人,随机分为两组,每组10例,即全麻复令硬膜外腔阻滞(GEA)组和全麻(GA)组,分别测定麻醉诱导前、手术2h、手术4h、术毕、术后1d及术后3d的血浆去甲肾上腺素、肾上腺素、血清促肾上腺皮质激素(ACTH)、皮质醇、C-反应蛋白、IL-6及IL-10的水平。结果 血浆去甲肾上腺素和血清皮质醇GEA组术中术后无显著改变,但GA组术毕和术后1d显著升高(P<0.05),术后3d恢复至术前水平,组间比较前者有显著差异(P<0.05)。两组血浆肾上腺素、IL-10术中术后均无显著变化。两组血清ACTH、IL-6及CRP术中术后均显著升高(P<0.05),组间比较无显著差异。结论 硬膜外腔阻滞可以减轻胸部手术的应激反应。IL-6是较CRP更灵敏的反映组织损伤的炎性指标。 相似文献
100.
40例乳腺癌根治术患者,美国麻醉医师协会(ASA)分级Ⅰ-Ⅱ级,随机分为2且,第1组硬膜外阻滞+臂丛神经阻滞,应用1.33%盐酸利多卡因+0.15%盐酸地卡因+1:20万肾上腺素,硬膜外阻滞首量12ml,臂丛神经阻滞20ml;第2组硬膜外阻滞,应用1.73%碳酸利多卡因+1:20万肾上腺素,首量15ml。两组硬膜外阻滞选为T4-5间隙穿刺。首量给完后测定麻醉药效,并监测患者心率(HR)、平均动脉压(MAP)、血氧饱和度(SpO2),在麻醉前、后30、60、120min抽取动脉血作血气分析。结果显示:第2组麻醉的起效时间、阻滞完善时间要比第1组短(P<0.01)。感觉神经阻滞分段数要比第1组多(P<0.01);两组病人的HR和MAP,麻醉手术中改变不明显。麻醉后面罩给氧。两组病人的SpO2、PaO2增加,PaCO2有所下降,两组比较无统计学意义,但组内前后对照有显著差异(P<0.05)。结果提示碳酸利多卡因硬膜外麻醉下施行乳腺癌根治术具有良好的麻醉效果和更高的安全性。 相似文献