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11.
12.
彩色多普勒超声和二维超声心动图并用,不仅可观察和了解心脏解剖、形态及腔室大小,又能观察血流动力学改变。我们从1991年11月至1992年11月间应用上述方法诊断先天性心脏病共18例,均经我院和外院手术证实:室间隔缺损7例;房间隔缺损6例;动脉导管未闭5例,其中1例误诊为肺动脉瓣狭窄,诊断准确率达94.4%。我们认为彩色多普勒诊断先天性心脏病方法安全,准确无损伤,为临床及术前提供了较可靠的诊断依据,但检查者必须了解心脏及大血管的解剖关系,结合临床才能提高诊断准确率,减少漏、误诊的发生。 相似文献
13.
Congenital pseudarthrosis of the clavicle is very rare. We report the results of two cases, one managed conservatively and
the second surgically. Neither patient had functional deficit, but the one treated surgically ended up with a scar, persisting
non-union and a short clavicle. Surgical treatment should be discouraged for this condition.
Received: 17 June 2002, Accepted: 17 July 2002 相似文献
14.
The posterior urethral valve uropathy: Results of treatment 总被引:2,自引:0,他引:2
Nineteen children treated for posterior urethral obstruction due to congenital valve in the University of Benin Teaching Hospital,
Benin City, Nigeria, over a 9-year period have been analysed. Their ages ranged from birth to 12 years. Results show that
associated kidney pathology may be irreversible even after successful excision of the valve. This determines the final prognosis,
which is worse the younger the child at presentation. 相似文献
15.
采用放射免疫法测定60例心血管病患儿的血浆心钠素,结果,在心功能不全,先天性心脏病、心肌炎者,明显高于正常组;心功能不全组明显高于非心功能不全组。非心功能不全的心血管疾患(如:先天性心脏病、心肌炎)之间无显著差异。说明血浆心钠素测定可作为心功能不全判断指标,并可指导治疗。 相似文献
16.
小儿先心病术后左房夺和肺动脉压力的监测在ICU中十分重要。心电图是论断和评价心脏疾患的常用方法。本文分析了32例小儿先心病手术前后(伴肺动脉高压16例)6个肢体导联心电图中P波和QRS波时限总和及振幅总和与左房、肺动脉压力的关系。结果表明两者均有良好的相关性(r=0.85 ̄0.88,r=0m74 ̄0.80,P〈0.01),该法简单、方便,可广泛开展,尤其在术后未放置PA和LA管或在IOU中已拨除L 相似文献
17.
RYUJI FUKAZAWA TAKASHI SEKI MITSUHIRO KAMISAGO MASANORI WATANABE SHUNICHI OGAWA KUNIO YUGE TSUNEO HIRAYAMA 《Pediatrics international》1994,36(4):427-430
We experienced a congenital complete atrioventricular block infant who was born from a Ro/SS-A antibody positive mother. Ro/SS-A antibody was also found in this baby which was presumed to be mediated by the maternal placenta. Temporary cardiac pacing was required at birth and pacemaker implantation was performed at 9 months. At 11 months of age, the baby fell into shock and experienced multiple organ failure because of diabetes mellitus-induced coma. The association between congenital complete heart block and the Ro/SS-A antibody is well known. However, the accompaniment of insulin-dependent diabetes mellitus has not been reported previously. As the Ro/SS-A antigen appears in the cytoplasm of many tissues, the possibility of an association between Ro/SS-A antibody and diabetes mellitus is difficult to deny. We report this rare case to draw attention to the possibility that babies who are born from an Ro/SS-A antibody positive mother may develop diabetes mellitus as well as congenital complete heart block. 相似文献
18.
P. KISS K. KOZLOWSKI E. ZAVODI 《Journal of Medical Imaging and Radiation Oncology》1991,35(3):266-267
A newborn with rhizomelic bone dysplasia with club-like femora is reported. This is the fourth case Of this easily recognizable, recently reported, congenital bone disease. Maroteaux et al recently reported two patients with rhizomelic bone dysplasia and club-like femora as a distinctive new bone dysplasia. Their observation was confirmed by Gugliantini et al (2) who reported another case. This paper reports a fourth patient with this easily recognisable disorder. 相似文献
19.
P. Pradat 《European journal of epidemiology》1992,8(6):789-796
This paper reports the results of a case-control study of major congenital heart defects (CHD) in Sweden. During the period 1981–1986, 1,324 such cases were identified and 2,648 controls were selected. Some common maternal characteristics and exposures were studied using information from prospectively collected data. Possible associations with CHD were found for previous perinatal death, maternal diabetes, epilepsy, hydramnios and disproportion between fetus and pelvis. More specific associations were observed between previous spontaneous abortion, epilepsy, hydramnios and truncus anomalies and between diabetes and septal anomalies. However, no associations were found with involuntary childlessness, contraceptive use, or smoking.Abbreviations ASD
atrial septal defect
- CHD
congenital heart defect
- CI
confidence interval
- CoA
coarctation of the aorta
- DORY
double outlet right ventricle
- ECD
endocardial cushion defect
- HLHS
hypoplastic left heart syndrome
- IUD
intrauterine device
- LMP
last menstrual period
- OC
oral contraceptive
- OR
odds ratio
- PDA
patent ductus arteriosus
- TGV
transposition of the great vessels
- VSD
ventricular septal defect 相似文献
20.
Efrat Rorman Chen Stein Zamir Irena Rilkis Hilla Ben-David 《Reproductive toxicology (Elmsford, N.Y.)》2006,21(4):458
Toxoplasma gondii (T. gondii) is the cause of toxoplasmosis. Primary infection in an immunocompetent person is usually asymptomatic. Serological surveys demonstrate that world-wide exposure to T. gondii is high (30% in US and 50–80% in Europe). Vertical transmission from a recently infected pregnant woman to her fetus may lead to congenital toxoplasmosis. The risk of such transmission increases as primary maternal infection occurs later in pregnancy. However, consequences for the fetus are more severe with transmission closer to conception. The timing of maternal primary infection is, therefore, critically linked to the clinical manifestations of the infection. Fetal infection may result in natural abortion. Often, no apparent symptoms are observed at birth and complications develop only later in life. The laboratory methods of assessing fetal risk of T. gondii infection are serology and direct tests.Screening programs for women at childbearing age or of the newborn, as well as education of the public regarding infection prevention, proved to be cost-effective and reduce the rate of infection.The impact of antiparasytic therapy on vertical transmission from mother to fetus is still controversial. However, specific therapy is recommended to be initiated as soon as infection is diagnosed. 相似文献