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11.
Cross sectional, M mode, and Doppler echocardiography, apexcardiography, and phonocardiography were used to characterise presystolic cardiovascular sounds in three patients with ventricular disease. Although the aetiology was different (dilated cardiomyopathy, primary pulmonary hypertension, and chronic pulmonary thromboembolic disease), in each case the presystolic sound was associated with a rapid change in acceleration of blood and with flow reversal in the superior vena cava, and could only be recorded at the right sternal edge or over the jugular veins. Such flow characteristics may be explained by a raised ventricular end diastolic pressure with reduced compliance. Use of these techniques helps to understand the cause of a previously described but little recognised heart sound, and adds weight to the interpretation of its presence in disease. 相似文献
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在微量注射大量肝脏mRNA之后,通过电压箝方法进行功能鉴定,两栖类卵母细胞成功地表达了AVPV1a受体。但在灌流AV4-8溶液时,却不能诱导卵母细胞产生内向振荡电流反应。提示AVP4-8不能通过AVPV1a受体而介导生理学效应。 相似文献
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Three kinds of lectins (UEA-I, ConA, PNA) were used to study normal, dysplastic, neoplastic nasopharyngeal epithelium by lectin affinitive histochemical method. UEA-I (ulex europeus agglutinin-I) displayed membrane distribution in normal squamous epithelium, but most of nasopharyngeal carcinoma cells were negative. Notably, severe dysplastic epithelium (precancerous lesion) exhibited a strong membranous and cytoplasmic affinity, which contrasted sharply with the normal epithelium and carcinoma cells. The statistically significant difference in the content and distribution of lectin UEA-I in these three groups suggest that UEA-I is a hopeful marker for diagnosing precancerous lesion of the nasopharynx. However, PNA and ConA are of less diagnostic value.
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目的:探讨血管内皮生长因子在肺癌中的表达情况与肺癌病理生物学行为之间的关系。方法:采用免疫组化SP法检测47例肺癌组织和10正常肺组织中VEGF的表达水平。结果:肺癌组织中VEGF的表达明显高于正常肺组织(P<0.005),P53、VEGF表达与肺癌的分化程度、淋巴结转移及P—TNM分期密切相关(P<0.05),与患者的性别、年龄、肿瘤大小及组织类型无关(P>0.05)。结论:检测肺癌组织中VEGF的表达水平有助于了解肿瘤的生物学行为,并可作为判断其预后的有价值指标。 相似文献
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目的:对中国药典收载的头孢噻肟钠聚合物测定条件进行改进。 方法 :采用高效液相色谱法 ,以Sephadex G- 10色谱柱 4 2 cm× 1.3cm对 6批样品进行分析 ,分别进样 5 0μl和 2 0 0μl,按外标法计算聚合物的量。结果:头孢噻肟钠在 10~ 6 0 μg/m l范围内线性关系良好 (r=0 .9995 ) ,高中低浓度的加样回收率分别为 10 0 .2 %、10 0 .4 %、99.7% ;RSD分别为 1.7%、1.5 %、1.9% (n =3)。该方法与药典方法比较 ,差异无统计学意义 (P >0 .0 5 )。 结论:本方法简便、快速、可行 ,具有实用价值 相似文献
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目的 对临床发生的急性输液反应进行分析,找出发生的原因,探讨预防措施。方法对201885例次输液治疗中的52例次输液反应资料进行分析。结果 经分析,属药物因素27例(52%),属操作因素11例(21%),属病人因素11例(21%),属输液器具因素3例(6%)。结论 把好药品和操作关,改善操作环境,严格操作规程是减少输液反应的关键。 相似文献
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目的:通过对患者在住院过程中的系统教育,使患者了解自己疾病的知识,提高患者对糖尿病的认知水平和自我管理能力,养成良好的健康行为和生活方式,从而提高生活质量。方法:采用集体、个体、自学等形式进行教育。结果:通过培养,患者掌握了一些基本的操作技能,明显缩短了住院日,同时激发了护士与患者学习专业知识的热情,减少或延缓了并发症的发生。结论:①健康教育是一个护患双边活动过程。②通过教育,可不断提高护士的自身修养和专业知识水平。③健康教育是糖尿病患者学习糖尿病知识,提高自我护理能力的有效途径。 相似文献
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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