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隐性脊柱裂、皮肤瘘管伴脊髓部小脑组织异位一例张劲松王翠娣马正中患者男,45岁,因左下肢麻木无力2日余,于1995年6月26日入院。患者于1995年4月开始感左下肢麻木不适,步行100米即感左下肢沉重无力,但无大小便障碍及阳萎。入院前1个月麻木加重,酸...  相似文献   
13.
采用放射免疫分析法对50例肝硬化门脉高压症患者手术前后血清四肽激素水平进行测定。结果:术前组血清四肽激素含量为580±187μg/L,脾大切组为667±172μg/L,全脾切除组为313±106μg/L,对照组为704±128μg/L;脾大部切除组血清四肽激素水平与对照组、术前组比较无显著差异(P>0.05);与全脾切除组比较有显著差异(P<0.01)。提示脾大部切除对血清四肽激素水平影响不大,而全脾切除使血清四肽激素水平下降。认为门脉高压症患者保脾更有重要的临床意义。  相似文献   
14.
本文使用一种测定α—磷酸甘油脱氢酶(α—GPD)活性的实验方法。本法其准确性较好,稀释实验和重复实验均符合要求,对大鼠肝、肺、肾、心、脑组织线粒体α—GPD 活性的测定结果与文献报道基本相符。  相似文献   
15.
Mechanisms of Cardioprotection by Volatile Anesthetics   总被引:2,自引:0,他引:2  
  相似文献   
16.
Background: Manipulations that cause hypersensitivity to visceral stimuli have been shown to also result in hypersensitivity to somatic stimuli coming from convergent dermatomes, but the converse has not been examined. The authors tested whether lumbar spinal nerve ligation in rats, a common model of neuropathic pain that results in hypersensitivity to somatic stimuli, also leads to hypersensitivity to visceral stimuli coming from convergent dermatomes and whether pharmacology of inhibition differed between these two sensory modalities.

Methods: Female Sprague-Dawley rats were anesthetized, and the left L5 and L6 spinal nerves were ligated. Animals received either intrathecal saline or milnacipran (0.1-3 [mu]g), and withdrawal thresholds to mechanical testing in the left hind paw, using von Frey filaments, and visceral testing, using balloon colorectal distension, were determined.

Results: Nerve ligation resulted in decreases in threshold to withdrawal to somatic mechanical stimulation (from 13 +/- 1.8 g to 2.7 +/- 0.7 g) and also in decreases in threshold to reflex response to visceral stimulation (from 60 mmHg to 40 mmHg). Intrathecal milnacipran increased withdrawal threshold to somatic stimulation in a dose-dependent manner but failed to alter the response to noxious visceral stimulation.  相似文献   

17.
Background: Volatile anesthetic preconditioning (APC) protects against myocardial ischemia-reperfusion (IR) injury, but the precise mechanisms underlying this phenomenon remain undefined. To investigate the molecular mechanism of APC in myocardial protection, the activation of nuclear factor (NF) [kappa]B and its regulated inflammatory mediators expression were examined in the current study.

Methods: Hearts from male rats were isolated, Langendorff perfused, and randomly assigned to one of three groups: (1) the control group: hearts were continuously perfused for 130 min; (2) the IR group: 30 min of equilibration, 15 min of baseline, 25 min of ischemia, 60 min of reperfusion; and (3) the APC + IR group: 30 min of equilibration, 10 min of sevoflurane exposure and a 5-min washout, 25 min of global ischemia, 60 min of reperfusion. Tissue samples were acquired at the end of reperfusion. NF-[kappa]B activity was determined by electrophoretic mobility shift assay. The NF-[kappa]B inhibitor, I[kappa]B-[alpha], was determined by Western blot analysis. Myocardial inflammatory mediators, including tumor necrosis factor [alpha], interleukin 1, intercellular adhesion molecule 1, and inducible nitric oxide synthase, were also assessed by Western blot analysis.

Results: Nuclear factor [kappa]B-DNA binding activity was significantly increased at the end of reperfusion in rat myocardium, and cytosolic I[kappa]B-[alpha] was decreased. Supershift assay revealed the involvement of NF-[kappa]B p65 and p50 subunits. APC with sevoflurane attenuated NF-[kappa]B activation and reduced the expression of tumor necrosis factor [alpha], interleukin 1, intercellular adhesion molecule 1, and inducible nitric oxide synthase. APC also reduced infarct size and creatine kinase release and improved myocardial left ventricular developed pressure during IR.  相似文献   

18.
Background: Adenosine triphosphate-regulated potassium channels mediate protection against myocardial infarction produced by volatile anesthetics and opioids. We tested the hypothesis that morphine enhances the protective effect of isoflurane by activating mitochondrial adenosine triphosphate-regulated potassium channels and opioid receptors.

Methods: Barbiturate-anesthetized rats (n = 131) were instrumented for measurement of hemodynamics and subjected to a 30 min coronary artery occlusion followed by 2 h of reperfusion. Myocardial infarct size was determined using triphenyltetrazolium staining. Rats were randomly assigned to receive 0.9% saline, isoflurane (0.5 and 1.0 minimum alveolar concentration [MAC]), morphine (0.1 and 0.3 mg/kg), or morphine (0.3 mg/kg) plus isoflurane (1.0 MAC). Isoflurane was administered for 30 min and discontinued 15 min before coronary occlusion. In eight additional groups of experiments, rats received 5-hydroxydecanoic acid (5-HD; 10 mg/kg) or naloxone (6 mg/kg) in the presence or absence of isoflurane, morphine, and morphine plus isoflurane.

Results: Isoflurane (1.0 MAC) and morphine (0.3 mg/kg) reduced infarct size (41 +/- 3%; n = 13 and 38 +/- 2% of the area at risk; n = 10, respectively) as compared to control experiments (59 +/- 2%; n = 10). Morphine plus isoflurane further decreased infarct size to 26 +/- 3% (n = 11). 5-HD and naloxone alone did not affect infarct size, but abolished cardioprotection produced by isoflurane, morphine, and morphine plus isoflurane.  相似文献   

19.
目的探讨儿童孤独症(CA)与多巴胺转运体(DAT1)440bp等位基因的关系。 方法陕西省纺织医院等于2004年3~8月,采用PCR技术对来自西安市两所康复中心的汉族CA儿童与DAT1基因多态性进行遗传关联分析。 结果(1)DAT1基因多态性中共观察到5种等位基因(320bp,360bp,440bp,480bp,520bp),6种基因型(480/480,480/320,520/480,480/360,480/440,440/440)。(2)使用相对危险度RR对CA与DAT1基因多态性的等位基因和基因型进行关联分析,显示480/440基因型和等位基因440与CA呈正关联,相对危险度分别为265和230,480/480基因型和等位基因480与CA呈负关联,相对危险度分别为064和077。但统计结果没有发现具有统计意义的差异。 结论中国汉族CA儿童与DAT1440bp等位基因无遗传关联。也许等位基因440bp与基因型480bp/440bp这两个因素是发病的风险因素,还有待今后的进一步研究。  相似文献   
20.
本文目的是检验一种用于量化和预测内镜检查患者的不良体验的一种问卷调查的可靠性。分别给予目前常规接受内镜检查的患者2份问卷(操作前及操作后)。第1份问卷包括人口统计学资料、既往内镜检查史、用药或饮酒史、患者期望值、操作前的焦虑及紧张程度。内镜检查后,重新确定患者的耐受性和意愿。内镜检查后对患者进行重复内镜检查的总体满意度或不情愿的主要结果评分≥5确定为“内镜检查的不良体验”(A EE)。148例受试者中有13例报告有AEE。通过对与不良反应如疼痛、紧张和操作期间的损伤情况明显相关的可靠分析,确定测定主要结果的项目。…  相似文献   
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