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海绵状血管瘤内压监测指导栓塞及硬化剂注射治疗 总被引:19,自引:0,他引:19
为探讨在栓塞硬化海绵状血管瘤中瘤腔内变化规律及其意义,在29例治疗过程中给机械性减缓交界本静脉回流,进行了瘤腔内压连续监测,发现:瘤腔基础内压力0.667~2.0kPa(1kPa=7.5mmHg)。颈部最低,回流快者所需栓塞次数多,用量大,瘤腔内压力曲线在栓塞初始为平台波形,提示回流静脉逐一被栓塞,随后出现缓慢下降的印峰波形,去除瘤体表浅回流静脉机械性压迫,瘤腔内压不变,提示回流静脉全部栓塞,可注 相似文献
23.
利用仿生化学的原理,本文设计并合成了两个儿茶酚胺类和两个羟基吡啶酮类八配位的螯合剂,初步动物试验表明,具有较强的钚促排能力。 相似文献
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Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq. 总被引:7,自引:5,他引:2 下载免费PDF全文
F Xiang Z Zhang A Clarke P Joseluiz N Sakkubai B Sarojini C D Delozier-Blanchet I Hansmann L Edstr?m M Anvret 《Journal of medical genetics》1998,35(4):297-300
Rett syndrome (RS) is a disease of neurological development. First reported 30 years ago in 1966, its biological and genetic basis remains obscure. RS is commonly thought of as an X linked dominant disorder lethal to hemizygous males. The few familial cases would arise through mosaicism or because of occasional females failing to manifest the disorder through skewed X inactivation in relevant cell types. We have one family where the mother and daughter are affected with RS, and which can be explained according to this hypothesis. If the alternative proposal of Thomas (1996) is correct, that the lack of males affected by such disorders is the result of a high male to female ratio of germline mutations rather than of gestational lethality, then the RS gene should be located on the grandpaternal chromosome. Genomic screening with markers covering the whole X chromosome has been performed. Studies using multiple informative markers indicate that the RS locus is likely to be located close to one of the X chromosome telomeres. Further investigations in eight additional families suggest the most likely region for the RS gene to be is the distal part of Xq (Xq28). 相似文献
26.
病理性近视眼的研究进展 总被引:5,自引:4,他引:1
通过复习近年来相关文献,对近视眼发生发展机制与形觉剥夺之间的关系进行综合评述。认为近视眼的发生及眼轴延长与形觉剥夺有一定关系,深入研究其相关机制,对近视眼的早期防治具有重要意义。 相似文献
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[目的]研究大豆蛋白对肾损害大鼠钙平衡的影响。[方法]选择3月龄断乳雄性SD大鼠40只.按体质量从小到大排序,采用完全随机化原则分为4组。每组10只。标准饲料对照组:喂食含有14%酪蛋白饲料;大豆蛋白饲料组:喂食含有14%大豆分离蛋白饲料;混合饲料1组:喂食含有7%酪蛋白加7%大豆分离蛋白饲料;混合饲料2组:喂食含有7%酪蛋白加14%大豆分离蛋白饲料。实验期用腺嘌呤灌胃共21d,建立肾损害大鼠模型,各组大鼠喂养相应饲料6周,测饲料消耗量、24h尿蛋白、尿钙、钙表观吸收率、储留钙量。[结果]4组实验大鼠饲料摄入量1d~30d无统计学差异,大豆蛋白饲料组和混合饲料1组实验结束时与另外两组相比,尿钙排泄量低,钙表观吸收率和储留钙量高,差异有统计学意义(P〈0.05)。[结论]蛋白质含量水平在14%条件下,含大豆蛋白的两种饲料对肾损害大鼠钙吸收、钙排泄的影响无统计学差异,有利于促进钙吸收,减少钙排泄。 相似文献
29.
Dong-Hai Xiong Hui Shen Peng Xiao Yan-Fang Guo Ji-Rong Long Lan-Juan Zhao Yao-Zhong Liu Hong-Yi Deng Jin-Long Li Robert R Recker Hong-Wen Deng 《Journal of bone and mineral research》2006,21(3):424-437
A genome-wide screen was conducted using a large white sample to identify QTLs for FNCS geometry. We found significant linkage of FNCS parameters to 20q12 and Xq25, plus significant epistatic interactions and sex-specific QTLs influencing FNCS geometry variation. INTRODUCTION: Bone geometry, a highly heritable trait, is a critical component of bone strength that significantly determines osteoporotic fracture risk. Specifically, femoral neck cross-sectional (FNCS) geometry is significantly associated with hip fracture risk as well as genetic factors. However, genetic research in this respect is still in its infancy. MATERIALS AND METHODS: To identify the underlying genomic regions influencing FNCS variables, we performed a remarkably large-scale whole genome linkage scan involving 3998 individuals from 434 pedigrees for four FNCS geometry parameters, namely buckling ratio (BR), cross-sectional area (CSA), cortical thickness (CT), and section modulus (Z). The major statistical approach adopted is the variance component method implemented in SOLAR. RESULTS: Significant linkage evidence (threshold LOD = 3.72 after correction for tests of multiple phenotypes) was found in the regions of 20q12 and Xq25 for CT (LOD = 4.28 and 3.90, respectively). We also identified eight suggestive linkage signals (threshold LOD = 2.31 after correction for multiple tests) for the respective geometry traits. The above findings were supported by principal component linkage analysis. Of them, 20q12 was of particular interest because it was linked to multiple FNCS geometry traits and significantly interacted with five other genomic loci to influence CSA variation. The effects of 20q12 on FNCS geometry were present in both male and female subgroups. Subgroup analysis also revealed the presence of sex-specific quantitative trait loci (QTLs) for FNCS traits in the regions such as 2p14, 3q26, 7q21 and 15q21. CONCLUSIONS: Our findings laid a foundation for further replication and fine-mapping studies as well as for positional and functional candidate gene studies, aiming at eventually finding the causal genetic variants and hidden mechanisms concerning FNCS geometry variation and the associated hip fractures. 相似文献
30.
The effects of combined use of earthworm extract(912)and HpD-laser on the produc-tion of reactive oxygen and the biosynthesis of DNA in S_(180) tumor cells were studied throughchemiluminescence measurement and[~3H]-TdR incorporation assay.The results showed that as com-pared with the control,the intensity of chemiluminescence emitted by tumor cells treatedsimultaneously with 912 and HpD-laser was enhanced more than ten-folds,while that treated with912 or HpD-laser alone was increased only 2~4 folds.The[~3H]-TdR incorporation into tumorcells of the former group was inhibited upto 74.1%,and that of the latter groups decreased onlyby 42.2% and 40.0%,respectively.In accordance with these biochemical changes,the ultrastructuraldamage of tumor cells of the former,combinedly treated group appeared to be the most serious.This suggests an additive effect of 912 with HpD-laser on tumor cells.In addition,if free radicalscavengers,such as catalase and superoxide dismutase,were added to the reaction systembefore chemiluminescence assay,the luminescent enhancement effect mentioned above was dramaticallyalleviated,implying the presence of O_2~ and H_2O_2 in the system.Therefore,as to the toxic effecton tumor cells,912 and HpD-laser are not only additive in efficiency,but also similar in theunderlying mechanism of action. 相似文献