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11.
输尿管上段结石的微创手术治疗 总被引:12,自引:0,他引:12
目的:探讨输尿管上段结石的治疗方法。方法:回顾性分析输尿管镜下气压弹道碎石(URSL),后腹腔镜输尿管切开取石(RLU)、经皮肾穿刺取石(PCNL)治疗输尿管上段结石患者的临床资料。其中URSL组25例,RLU组20例。PCNL组9例。结果:URSL组碎石成功18例;7例不成功,其中3例改为开放手术,1例改为后腹腔镜取石。2例行ESWL术,1例仅留置双J管。术后1个月拔管后自行排出。2例并发输尿管穿孔。RLU组取石成功18例,2例滑入肾内,经配合输尿管镜和腹腔镜直视下经皮肾穿刺取石成功,术后15例有伤口漏尿。PCNL组成功9例,无并发症。结论:USRL创伤小。术后恢复快。是治疗输尿管上段结石的较为满意的治疗方法。PCNL创伤小,取石成功率高,在结石靠近肾盂、儿童输尿管上段结石并同侧肾结石和结石以下输尿管狭窄时应优先考虑。但技术难度较大。RLU可作为URSL不成功后的辅助治疗方法。 相似文献
12.
目的:了解TGF-β受体和整合素在瘢痕增生和挛缩过程中的作用.方法:通过荧光定量PCR法(FQ-PCR)测定经TGF-β受体、整合素和粘着斑激酶(FAK)抗体阻断后培养的瘢痕成纤维细胞TGF-β受体以及整合素表达量的变化.结果:经不同抗体阻断后培养的瘢痕成纤维细胞其TGF-β RI和整合素β 1的基因拷贝数均较阴性对照组有不同程度的下降(P<0.05).结论:TGF-β受体和整合素介导的信号传导途径间可能存在着正反馈的效应,共同促进瘢痕的增生和挛缩.FAK是两条信号传导途径的交汇点和作用的中心环节. 相似文献
13.
系统性健康教育对改善焦虑病人症状的影响 总被引:1,自引:1,他引:0
焦虑症是以焦虑、紧张、恐惧等情绪障碍为主,常伴有自主神经系统症状和运动性不安等[1].主要表现为惊恐发作和广泛性焦虑两种形式.随着社会的发展、生活节奏的加快、竞争的激烈、社会分工的多元化、婚姻的变故、考试的不理想等生活事件,使人们的精神压力大为增加[2].以往的传统求稳心态已落后于时代的发展,一种以焦虑情绪为主的神经症已成为一个时代的现代疾病.焦虑症的发展有逐年上升的趋势,已受到更多人的关注和注意.对焦虑症病人实施系统性的健康教育,降低焦虑症的复发率具有重要的意义.…… 相似文献
14.
G. Wu S. F. Fan Z.-H. Lu R. W. Ledeen S. M. Crain 《Journal of neuroscience research》1995,42(4):493-503
Prolongation of the action potential duration of dorsal root ganglion (DRG) neurons by low (nM) concentrations of opioids occurs through activation of excitatory opioid receptors that are positively coupled via Gs regulatory protein to adenylate cyclase. Previous results suggested GM1 ganglioside to have an essential role in regulating this excitatory response, but not the inhibitory (APD-shortening) response to higher (μM) opioid concentrations. Furthermore, it was proposed that synthesis of GM1 is upregulated by prolonged activation of excitatory opioid receptor functions. To explore this possibility we have utilized cultures of hybrid F11 cells to carry out closely correlated electrophysiological and biochemical analyses of the effects of chronic opioid treatment on a homogeneous population of clonal cells which express many functions characteristic of DRG neurons. We show that chronic opioid exposure of F11 cells does, in fact, result in elevated levels of GM1 as well as cyclic adenosine monophosphate (AMP), concomitant with the onset of opioid excitatory supersensitivity as manifested by naloxone-evoked decreases in voltage-dependent membrane K+ currents. Such elevation of GM1 would be expected to enhance the efficacy of excitatory opioid receptor activation of the Gs/adenylate cyclase/cyclic AMP system, thereby providing a positive feedback mechanism that may account for the remarkable supersensitivity of chronic opioid-treated neurons to the excitatory effects of opioid agonists as well as antagonists. These in vitro findings may provide novel insights into the mechanisms underlying naloxone-precipitated withdrawal syndromes and opioid-induced hyperalgesia after chronic opiatf addiction in vivo. © 1995 Wiley-Liss, Inc. 相似文献
15.
The objective of this study was to determine whether the development of tolerance to CP 55,940, a potent cannabinoid agonist, was due to changes in the receptor or second messenger system. ICR mice treated with CP 55,940 (2 mg/kg) twice a day for 6 and one-half days developed a high degree of tolerance to the pharmacological effects of CP 55,940. The ability of CP 55,940 to produce motor hypoactivity, hypothermia and immobility was reduced 163-, 97- and 19-fold, respectively. Evaluation of 3H-CP 55,940 binding to rat brain membranes indicated no difference in receptor affinity between the vehicle- and CP 55,940-treated animals. However, these binding studies revealed a 50% decrease in receptor number in the cerebellum of the CP 55,940-tolerant mice. Although cAMP is generally considered to be the second messenger for cannabinoid receptors, little difference was observed in the inhibitory effects of CP 55,940 on adenylyl cyclase activity in cerebellum between vehicle and drug-treated mice. However, there was an increase in receptor mRNA which suggests a compensation for receptor loss. There are several possible explanations for these results. There may be sufficient spare receptors such that CP 55,940-tolerant mice are capable of producing a maximal effect on the second messenger system. On the other hand, one could conclude that cannabinoid receptor down-regulation does not account for the development of tolerance to all of the effects of CP 55,940 in mice. 相似文献
16.
实验国际学校学生膳食及营养状况的调查 总被引:2,自引:0,他引:2
本文对南京实验国际学校369名6~11岁学生进行了膳食及营养状况的分析研究。结果表明:该校学生膳食中除视黄醇、钙及锌(9~11岁组)不足外,其余营养素和热能均超过推荐供应量。蛋白质量足质优。脂肪在一天总热能中比例较高.达到30%左右。该校学生营养过剩发生率达18.4%.提示该校食堂要注意学生膳食的合理调配.防止学生摄入过多脂肪和热能;同时建议增加含钙、锌高的食物供给,以补充其不足。 相似文献
17.
乡(镇)卫生院是农村三级医疗预防保健网的中心环节,是我国农村实现“2000年人人享有卫生保健”的关键。本文通过对广东省梅县乡(镇)一级卫生院卫生人力状况的调查分析,结果表明,目前该县乡镇卫生院的机构稳定,卫技人员占编比例合理,年龄较轻,成为今后农村卫生院发展的优势。但存在着卫生技术人员的总体数量不足,素质较差,各类专业技术人员的构成比例失调和层次分布不合理等问题,同时提出了如何加以改善的对策措施。 相似文献
18.
Evidence that [3H]-alpha,beta-methylene ATP may label an endothelial-derived cell line 5'-nucleotidase with high affinity. 总被引:1,自引:1,他引:0 下载免费PDF全文
A. D. Michel N. M. Chau T. P. Fan E. E. Frost P. P. Humphrey 《British journal of pharmacology》1995,115(5):767-774
1. In membranes prepared from a permanent cell line of endothelial origin (WEC cells), [3H]-alpha, beta-methylene ATP ([3H]-alpha, beta-meATP) labelled high (pKd = 9.5; Bmax = 3.75 pmol mg-1 protein) and low (pKd = 7.2; Bmax = 23.3 pmol mg-1 protein) affinity binding sites. The high affinity [3H]-alpha, beta-meATP binding sites in the WEC cell membranes could be selectively labelled with a low concentration of the radioligand (1 nM). In competition studies performed at a radioligand concentration of 1 nM, 88.6% of the sites possessed high affinity (pIC50 = 8.26) for alpha, beta-meATP. 2. The high affinity [3H]-alpha, beta-meATP binding sites appeared heterogeneous since in competition studies a number of nucleotide analogues (alpha, beta-meADP, ATP, ADP, AMP, GTP, GppNHp, GMP) and adenosine identified two populations of the sites labelled by 1 nM [3H]-alpha, beta-meATP. The proportion of sites with high affinity for these compounds was found to vary between 42 and 69%. 3. Approximately 60-69% of the binding sites labelled with 1 nM [3H]-alpha, beta-meATP possessed high affinity for alpha, beta-meADP (pIC50 = 8.87), AMP (pIC50 = 7.12), GMP (pIC50 = 7.34), UTP (pIC50 = 6.12), GTP (pIC50 = 7.59), GppNHp (pIC50 = 7.35) and adenosine (pIC50 = 5.45).(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
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