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Gabriella M van Dijk Cindy Veenhof Francois Schellevis Harry Hulsmans Jan PJ Bakker Henk Arwert Jos HM Dekker Guus J Lankhorst Joost Dekker 《BMC musculoskeletal disorders》2008,9(1):95
Background
This study aims to contribute to the knowledge of the influence of comorbidity in OA. The objectives of the study were (i) to describe the prevalence of comorbidity and (ii) to describe the relationship between comorbidity (morbidity count, severity and the presence of specific diseases) and limitations in activities and pain in elderly patients with knee or hip OA using a comprehensive inventory of comorbidity. 相似文献73.
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Distribution and Genetic Diversity of Suilysin in Streptococcus suis Isolated from Different Diseases of Pigs and Characterization of the Genetic Basis of Suilysin Absence 总被引:5,自引:0,他引:5
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Samantha J. King Peter J. Heath Inmaculada Luque Carmen Tarradas Christopher G. Dowson Adrian M. Whatmore 《Infection and immunity》2001,69(12):7572-7582
Streptococcus suis is an economically important pathogen of pigs responsible for a variety of diseases including meningitis, septicemia, arthritis, and pneumonia, although little is known about the mechanisms of pathogenesis or virulence factors associated with this organism. Here, we report on the distribution and genetic diversity of the putative virulence factor suilysin, a member of the thiol-activated toxin family of gram-positive bacteria. On the basis of PCR analysis of over 300 isolates of S. suis, the suilysin-encoding gene, sly, was detected in 69.4% of isolates. However, sly was present in a considerably higher proportion of isolates obtained from cases of meningitis, septicemia, and arthritis (>80%) and isolates obtained from asymptomatic tonsillar carriage (>90%) than lung isolates associated with pneumonia (44%). With the exception of serotypes 1, 14, and 1/14, there was no strong correlation between the presence of suilysin and serotype. Analysis of the genetic diversity of suilysin by restriction fragment length polymorphism and sequence analysis found that the suilysin gene, where present, is highly conserved with a maximum of 1.79% diversity at the nucleotide level seen between sly alleles. Assays of hemolytic activity and hybridization analysis provided no evidence for a second member of the thiol-activated toxin family in S. suis. Inverse PCR was used to characterize regions flanking sly, which in turn allowed the first characterization of the equivalent region in a strain lacking sly. Sequence comparison of these regions from sly-positive (P1/7) and sly-negative (DH5) strains indicated that two alternative arrangements are both flanked by genes with highest similarity to haloacid dehalogenase-like hydrolases (5' end) and putative N-acetylmannosamine-6-phosphate epimerases (3' end). However, sly appears to be completely absent from the alternative arrangement, and a gene of unknown function is located in the equivalent position. Finally, PCR analysis of multiple sly-positive and -negative strains indicated that these two alternative genetic arrangements are conserved among many S. suis isolates. 相似文献
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A modified version of the revised Personality Diagnostic Questionnaire (PDQ-R), based on DSM-III-R personality disorders (PD), was completed by 74 psychiatric patients. A factor analysis of the scores for each of the PD (i.e. of the number of positive DSM-III-R criteria for each of the PD) yielded 3 factors that defined 3 PD clusters. These were similar to the 3 DMS-III-R PD clusters for 7 of the 11 PD categories. The 3-group solution of a cluster analysis of the patients (using their scores of positive criteria for each of the PD) did not reflect these factors; the main discriminating variable between the 3 groups of patients was the total number of positive PD criteria. It is suggested that, for the routine assessment of patients, the most important derivative of the DSM-III-R classification of PD is the total score of positive PD criteria. 相似文献
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Rubin JI; Arger PH; Pollack HM; Banner MP; Coleman BG; Mintz MC; VanArsdalen KN 《Radiology》1987,162(1):21
79.
目的:分析一遗传性牙釉质发育不全家系的发病情况及病变特征,明确其遗传方式,为进一步基因定位和克隆奠定基础。方法:2003-05在中国山东某市发现一遗传性牙釉质发育不全家系,先证者为1名43岁男性牙釉质发育不全患者。该家系现存活3代,共有36名家庭成员。对先证者及其家族进行口腔检查和全身检查,制备牙齿磨片镜下观察,对该患者及其亲属成员进行家系调查,系谱分析,明确可能的遗传方式。结果:①口腔及全身临床表现:口腔检查可见大量牙石,釉质病变涉及全口牙齿,牙体呈黄褐色,磨耗重,釉质易碎裂剥脱。X射线显示牙釉质密度基本与牙本质相同,髓腔形态未见异常。临床表现符合Witkop1989年分类中的钙化不全型牙釉质发育。全身系统检查排除系统性疾病。无四环素用药史,家族中无近亲结婚者,附近居民无相似病变。②牙齿磨片观察结果:可见釉丛及釉板明显,且数目增多,表明釉质发育较差。③遗传方式:该家系36名成员,3代中均有患者,共检出遗传性牙釉质发育不全患者13人,其中男7例,女6例,传递方式符合常染色体显性遗传的特点。结论:该家系为常染色体显性遗传性钙化不全型牙釉质发育不全家系,为下一步定位该家系致病基因奠定基础。 相似文献
80.
The Treatment of Septicemia in Pacemaker Patients 总被引:5,自引:0,他引:5
ÁDÁM BÖHM FERENC BÁNYAI ISTVÁN PRÉDA KÁROLY ZÁMOLYI 《Pacing and clinical electrophysiology : PACE》1996,19(7):1105-1111
The authors analyzed the data of seven patients who had undergone open heart surgery because of pacemaker endocarditis in the past 4 years. Repeated surgical interventions on the pacemaker system were found to be the most common predisposing factors. Staphylococcus aureus and Staphylococcus epidermidis were the most common causative organisms. Two-dimensional echocardiography was important in the diagnosis of cases with atypical clinical picture and negative blood cultures. We concluded that: (1) any pacemaker patient with fever should be considered to have a pacemaker endocarditis; (2) all of these patients should be examined by two-dimenensional echocardiography; and (3) the total removal of the infected hardware seems to be the only way to achieve complete recovery. 相似文献