全文获取类型
收费全文 | 53465篇 |
免费 | 5456篇 |
国内免费 | 3972篇 |
专业分类
耳鼻咽喉 | 519篇 |
儿科学 | 768篇 |
妇产科学 | 916篇 |
基础医学 | 5823篇 |
口腔科学 | 933篇 |
临床医学 | 6725篇 |
内科学 | 7627篇 |
皮肤病学 | 512篇 |
神经病学 | 2841篇 |
特种医学 | 1946篇 |
外国民族医学 | 24篇 |
外科学 | 6046篇 |
综合类 | 9395篇 |
现状与发展 | 14篇 |
一般理论 | 6篇 |
预防医学 | 4015篇 |
眼科学 | 1083篇 |
药学 | 5782篇 |
46篇 | |
中国医学 | 3453篇 |
肿瘤学 | 4419篇 |
出版年
2024年 | 236篇 |
2023年 | 951篇 |
2022年 | 2365篇 |
2021年 | 3041篇 |
2020年 | 2294篇 |
2019年 | 1925篇 |
2018年 | 1921篇 |
2017年 | 1937篇 |
2016年 | 1702篇 |
2015年 | 2637篇 |
2014年 | 3279篇 |
2013年 | 3166篇 |
2012年 | 4362篇 |
2011年 | 4453篇 |
2010年 | 3067篇 |
2009年 | 2387篇 |
2008年 | 2972篇 |
2007年 | 2776篇 |
2006年 | 2550篇 |
2005年 | 2520篇 |
2004年 | 1704篇 |
2003年 | 1674篇 |
2002年 | 1395篇 |
2001年 | 1107篇 |
2000年 | 1055篇 |
1999年 | 975篇 |
1998年 | 566篇 |
1997年 | 551篇 |
1996年 | 440篇 |
1995年 | 419篇 |
1994年 | 379篇 |
1993年 | 235篇 |
1992年 | 314篇 |
1991年 | 276篇 |
1990年 | 228篇 |
1989年 | 174篇 |
1988年 | 183篇 |
1987年 | 141篇 |
1986年 | 131篇 |
1985年 | 89篇 |
1984年 | 59篇 |
1983年 | 47篇 |
1982年 | 23篇 |
1981年 | 19篇 |
1980年 | 26篇 |
1979年 | 26篇 |
1978年 | 16篇 |
1977年 | 14篇 |
1976年 | 9篇 |
1970年 | 10篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
Shengxuan Cao Chen Wang Xin Ma Xu Wang Jiazhang Huang Chao Zhang Li Chen Xiang Geng Kan Wang 《Journal of orthopaedic research》2019,37(8):1860-1867
Patients with mechanic ankle instability experience increased tibiotalar and subtalar joint laxity. However, in vivo joint kinematics in functional ankle instability (FAI) patients and lateral ankle sprain (LAS) copers, especially during dynamic activities, are poorly understood. Ten FAI patients, 10 LAS copers, and 10 healthy controls were included in this study. A dual fluoroscopic imaging system was used to analyze the tibiotalar and subtalar joint kinematics during stair descent. Five key poses of stair descent were analyzed. Kinematic data from six degrees of freedom were calculated utilizing a solid modeling software. The range of motion and joint positions in each degree of freedom were compared among the three groups. The tibiotalar joints of FAI patients and LAS copers were significantly more inverted than those of healthy controls during the foot strike (p = 0.016, = 0.264). The subtalar joints of FAI patients were significantly more anteriorly translated (pose 2, p = 0.003, = 0.352; pose 3, p < 0.001, = 0.454; pose 4, p = 0.004, = 0.334), inverted (pose 4, p = 0.027, = 0.234; pose 5,p = 0.034, = 0.221), and externally rotated (pose 4, p = 0.037, = 0.217; pose 5; p = 0.004, = 0.331) than those of healthy controls during the mid‐stance and the heel off. The FAI patients showed excessive tibiotalar inversion and subtalar joint hypermobility during stair descent. Meanwhile, the LAS copers maintained subtalar joint stability, and only showed excessive tibiotalar inversion in foot strike. These data provide insight into the mechanisms behind the development of FAI after initial LAS. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:1860–1867, 2019 相似文献
2.
3.
Background
Aromatic l-amino acid decarboxylase (AADC) deficiency (OMIM #608643) is a rare and severe disorder of biogenic amine synthesis caused by mutations in the DDC gene. The phenomenology of the movement disorder includes intermittent oculogyric crises and limb dystonia, generalized athetosis, and impaired voluntary movement.Objective
To identify clinical manifestations and DDC gene mutations in two Chinese mainland children who are siblings with AADC deficiency.Methods
We used targeted next-generation sequencing and quantitative polymerase chain reaction (qPCR) to reveal DDC mutations in these children.Results
Two DDC gene mutations were found: one missense mutation, c.1040G?>?A (p.Arg347Gln), is a reported mutation derived from the mother; the other mutation, a whole-exon 11 and 12 deletion, is a novel mutation derived from the father. The index patient and her brother both had poor sucking power and feeding difficulty at birth and episodes of oculogyric crises, truncal hypotonia, limb hypertonia, sleep disturbances, irritability, and motor delay. The siblings both died at 1?year and 10?months due to asphyxia and pneumonia during gaze and hypertonia episodes.Conclusion
This study identified a novel DDC gene deletion mutation in two siblings with AADC deficiency disease in the Chinese mainland population. 相似文献4.
目的以冰粒子为致孔剂,用粒子滤出—冷冻干燥复合工艺制备PHB多孔支架。方法本实验以氯仿为溶剂,将PHB溶液浇入预先排列好的冰微粒空隙中,采用真空渗流方法制备冰微料-PHB复合体,液氮冷却成型后,用粒子滤出—冷冻干燥复合工艺制备多孔支架。通过扫描电镜(SEM)观测,研究该制备工艺对支架形貌的影响。结果制备的块状三维多孔支架孔径可调、孔隙结构良好、孔隙连通度高。结论本文工艺所制备的多孔支架无致孔剂残留,孔隙率高,孔隙连通度高,制备过程不会损害材料的生物相容性,可安全地用于组织工程可降解聚合物多孔支架的制备。 相似文献
5.
Mary Ann Richardson Helen M Chao Laura L Read James D Clelland Raymond F Suckow 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2006,(2):195-197
Phenylketonuria (PKU), an inborn error of phenylalanine metabolism, has been shown to be a risk factor for tardive dyskinesia (TD). In male psychiatric patients there was a significant relationship between TD and measures of plasma phenylalanine following ingestion of a standardized phenylalanine dose that was indicative of higher brain availability of phenylalanine in patients with TD. In addition, a medical food formulation consisting of branched chain amino acids, which compete with phenylalanine for transport across the blood-brain barrier, has been demonstrated to be an efficacious treatment for TD. Cumulatively these findings suggested that TD was related to phenylalanine metabolism and thus that sequence variants in the gene for phenylalanine hydroxylase (PAH), the rate-limiting enzyme in the catabolism of phenylalanine, could be associated with TD susceptibility. Genetic screening of PAH in a group of 123 psychiatric patients revealed ten sequence polymorphisms and two mutations, but none appeared to be a significant risk factor for TD. 相似文献
6.
7.
β-胡萝卜素立体异构体对环磷酰胺处理小鼠免疫功能的比较研究 总被引:3,自引:0,他引:3
就β-胡萝卜素立体异构体对环磷酰胺处理小鼠的免疫功能影响进行了比较研究。结果显示β-胡萝卜素立体异构体对外磷酰胺造成的免疫功能低下具有不同程度的改善作用,提高胸腺和脾脏指数,增强脾脏细胞对刀豆素A(ConA)的反应性和NK活性,血清溶菌酶含量也有所增加。综合各项指标,9-顺式和全反式混合物的作用最明显,提示一定浓度的9-顺式对于提高β-胡萝卜素对机体的总体作用是有一定意义的。 相似文献
8.
Two unique forms of cytochrome P-450 (P-450), designated NMa and NMb, were recently isolated in this laboratory from nasal microsomes of rabbits. In the present study, polyclonal antibodies to the purified nasal cytochromes were prepared. Immunochemical analysis with specific rabbit anti-NMa and sheep anti-NMb antibodies indicated that P-450 isozymes identical to or having a high structural homology with NMa are present in both olfactory and respiratory mucosa, as well as in liver, but NMb was detected only in the olfactory mucosa. Neither form was detected in other tissues examined, including brain, esophageal mucosa, heart, intestinal mucosa, kidney, and lung. The specific occurrence of NMb in the olfactory mucosa was further substantiated by the detection and specific inhibition by anti-NMb of the formation of unique NMb-dependent metabolites of testosterone in olfactory microsomes but not in microsomes from liver or respiratory mucosa. Similar experiments with antibodies to previously purified rabbit hepatic P-450 isozymes indicated that not all of the hepatic cytochromes are expressed in the nasal tissues. Thus, P-450 isozymes structurally homologous to hepatic forms 2, 3a, and 4, but not 3b and 6, were found in the olfactory mucosa. On the other hand, only form 2 was detected in the respiratory mucosa. Immunoquantitation experiments revealed that NMa and NMb are the major P-450 forms in olfactory microsomes, whereas NMa and P-450 form 2 (or its homolog) constitute the major portion of the respiratory nasal microsomal P-450. The level of NMa in the liver is relatively low, accounting for less than 3% of total microsomal P-450 in this tissue. In addition, evidence is provided that NMa is the major catalyst in the dealkylation of two nasal carcinogens, hexamethylphosphoramide and phenacetin, in both olfactory and respiratory nasal microsomes. 相似文献
9.
10.
目的:探讨EB病毒感染与人大肠癌发生的关系。方法:用原位分子杂交法对130例人大肠癌标本中EB病毒小分子RNA片段进行检测。结果:130例标本中有6例(4.48%)癌组织呈阳性反应,其中4例为男性,4例有明显淋巴细胞浸润。结论:EB病毒感染可能与我国部分大肠腺癌的发生有关,肿瘤细胞间质中大量淋巴细胞浸润可能是EB病毒感染的重要病理学特征。 相似文献