全文获取类型
收费全文 | 62336篇 |
免费 | 3011篇 |
国内免费 | 323篇 |
专业分类
耳鼻咽喉 | 870篇 |
儿科学 | 1173篇 |
妇产科学 | 974篇 |
基础医学 | 8255篇 |
口腔科学 | 1609篇 |
临床医学 | 4183篇 |
内科学 | 15285篇 |
皮肤病学 | 1110篇 |
神经病学 | 5005篇 |
特种医学 | 2259篇 |
外科学 | 10659篇 |
综合类 | 282篇 |
一般理论 | 2篇 |
预防医学 | 1998篇 |
眼科学 | 1185篇 |
药学 | 4756篇 |
中国医学 | 111篇 |
肿瘤学 | 5954篇 |
出版年
2023年 | 313篇 |
2022年 | 656篇 |
2021年 | 1105篇 |
2020年 | 584篇 |
2019年 | 801篇 |
2018年 | 1043篇 |
2017年 | 804篇 |
2016年 | 989篇 |
2015年 | 1060篇 |
2014年 | 1447篇 |
2013年 | 1785篇 |
2012年 | 2905篇 |
2011年 | 3207篇 |
2010年 | 1831篇 |
2009年 | 1594篇 |
2008年 | 2973篇 |
2007年 | 3263篇 |
2006年 | 3191篇 |
2005年 | 3297篇 |
2004年 | 3272篇 |
2003年 | 3335篇 |
2002年 | 3166篇 |
2001年 | 1888篇 |
2000年 | 1992篇 |
1999年 | 1803篇 |
1998年 | 852篇 |
1997年 | 680篇 |
1996年 | 648篇 |
1995年 | 556篇 |
1994年 | 507篇 |
1993年 | 453篇 |
1992年 | 1267篇 |
1991年 | 1060篇 |
1990年 | 1025篇 |
1989年 | 1052篇 |
1988年 | 945篇 |
1987年 | 923篇 |
1986年 | 879篇 |
1985年 | 861篇 |
1984年 | 620篇 |
1983年 | 497篇 |
1982年 | 286篇 |
1980年 | 249篇 |
1979年 | 534篇 |
1978年 | 322篇 |
1977年 | 297篇 |
1975年 | 239篇 |
1974年 | 249篇 |
1971年 | 249篇 |
1969年 | 244篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
A statistical study was carried out on the incidence of CDH associated with mechanical factors in the uterus, including congenital genu recurvatum. There were 72 cases of CDH among 6559 infants (1.1 per cent). The incidence of CDH was 0.7 per cent in cephalic presentation, 2 per cent in footling presentation and 20 per cent in single-breech presentation. In another series, CDH was found in six of seven infants with congenital genu recurvatum. These findings suggest that a fetal posture with the hip flexed and the knee extended predisposes to the development of CDH. 相似文献
42.
43.
44.
Changes in central dopaminergic systems with the expression of Shh or GDNF in mice perinatally exposed to bisphenol-A. 总被引:1,自引:0,他引:1
Kazuya Miyagawa Minoru Narita Michiko Narita Keiichi Niikura Hisahiko Akama Yuri Tsurukawa Tsutomu Suzuki 《Nihon shinkei seishin yakurigaku zasshi》2007,27(2):69-75
In the previous study, we reported that exposure to bisphenol-A induced the potentiation of dopamine receptor functions in the mouse limbic area, resulting in supersensitivity to methamphetamine-induced pharmacological actions. The present study was undertaken to investigate whether prenatal exposure to bisphenol-A could produce morphological change in dopaminergic neuron and the pattern of expression of genes regulating the dopaminergic neuron development. Here we found that prenatal and neonatal exposures to bisphenol-A increased the tyrosine hydroxylase- and dopamine transporter-like immunoreactivities in the adult mouse limbic area. The present molecular biological study shows that chronic bisphenol-A treatment produced a significant decrease in the dopaminergic neuron development factors, sonic hedgehog and glial cell line-derived neurotrophic factor, which were also decreased by prenatal exposure to bisphenol-A. These results suggest that chronic exposure to bisphenol-A could disrupt the dopaminergic neurotransmission in the process of dopaminergic neuron development. 相似文献
45.
Harukazu Suzuki 《The Journal of physiology》2006,575(2):373-377
Recent genome-wide high-throughput (HTS) analyses of protein–protein interactions (PPIs) provide molecular-based information to uncover functions of cells and tissues, such as those of the mammalian brain. However, the HTS PPI data contain much false-negatives and false-positives, which should be primarily addressed in experiments. Integrating PPI data sets with other genome-wide data, such as expression profiles and phenotype data sets, provides novel biological insights. Such integration analysis is valuable for addressing the complexity of the mammalian brain. Discovery of novel interactions followed by a detailed analysis is a successful approach to uncover the function of proteins. For example, extensive PPI screens for parkin , a hereditary Parkinson's disease gene, elucidated the function of parkin as an E3 ubiquitin ligase, with localization and activity regulated by contact with its interaction partners, uncovering at least a part of the molecular pathogenesis of Parkinson's disease. 相似文献
46.
Yasuo Suzuki 《Journal of neuro-ophthalmology》2007,27(2):138-142
Kenji Ohtsuka, MD and his colleagues at the Sapporo Medical University have investigated the central organization of the near response with anatomical and neurophysiologic studies in cats. Based on their data and clinical observations, they proposed that the rostral pole of the superior colliculus has a critical role in the control of accommodation, vergence, and fixation. Although the central pathways have yet to be fully worked out, the contributions of Dr. Ohtsuka, who died in 2005, have laid an important foundation in the understanding of these functions. 相似文献
47.
Akihiro Shindo Yasumasa Kokubo Akira Taniguchi Manami Kuze Shigeki Kuzuhara 《Clinical neurology》2007,47(2-3):116-118
A 30-year-old woman was admitted to Mie University Hospital for recurrence of sudden visual field defect with photopsia in the right eye. She had experienced the same episodes at the age of 15, 20, 25 and 28 years old. A diagnosis of retrobulbar optic neuritis had been made at each episode, but corticosteroid therapy failed to resolve the symptoms. Neurologic examination on admission was unremarkable except for the visual field defect of the right eye. Brain MRIs with and without gadolinium enhancement were normal. On ophthalmologic examination, visual acuity was normal, but the Mariotte blind spot of the right eye was expanded. Ophthalmoscopic examination, visual evoked potential, flicker electro-oculogram and Hess test were normal. Multifocal electroretinogram (ERG) revealed reduction in the inferior temporal response of the right eye that corresponded to the expansion of the Mariotte blind spot These findings were consistent with conditions of acute zonal occult outer retinopathy (AZOOR). The visual symptoms of AZOOR thus resemble those of retrobulbar optic neuritis and findings of multifocal ERG were useful to differentiate them. AZOOR is a newly established condition, and it is necessary to pay more attention to AZOOR on the differential diagnoses of acute-onset mono ocular visual disturbances. 相似文献
48.
49.
S Miyajima Y Aizawa K Suzuki M Satoh S Niwano K Ebe T Fujita J Ishiguro Y Hirokawa A Shibata 《Japanese heart journal》1989,30(2):241-249
Recently, we examined 2 cases of hypertrophic cardiomyopathy (HCM) presenting with sustained ventricular tachycardia (VT). One case was a 62 year old male with midventricular hypertrophy and monomorphic sustained VT. After admission, the efficacies of procainamide, disopyramide, aprindin, flecainide, mexiletine and verapamil were evaluated by means of continuous electrocardiographic monitoring. Verapamil prevented the recurrence of sustained VT and markedly reduced the frequency and number of runs of nonsustained VT. In the electrophysiologic study, rapid VT was induced by double extrastimuli at the right ventricular apex. Intravenous verapamil at a dose of 10 mg prevented the induction of VT. The patient was discharged on verapamil and remains asymptomatic after 3 months of follow up. The other case was a 34 year old female who was a survivor of cardiac arrest. Monomorphic VT was observed on emergency admission and was converted to sinus rhythm by direct current cardioversion after resuscitation. In the electrophysiologic study, rapid VT was induced by double extrastimuli at the right ventricular outflow tract. Verapamil at a dose of 10 mg prevented the induction of VT. These 2 cases of HCM are rare in that they presented with sustained VT. It is also of interest that verapamil, which has been used conventionally in HCM, prevented VT. 相似文献
50.
The genetic program that drives tumor metastasis and the mode and timing of its initiation are of great practical significance to clinical management. Modern technical advances open new opportunities for gaining useful relevant information. Gene expression profiles of histologically‐verified viable tissue from lymph node metastases were compared with those of matched primary breast cancers from 10 different patients, among samples from over 400 cases, using high‐throughput oligonucleotide arrays comprising probes for 22,000 genes. It was observed that metastases have very similar expression signatures to their parent tumors. However, detailed computational analysis revealed that a small number of genes were consistently differentially expressed between 100% of tumors and metastases, suggesting that these are mechanistically important. Lists of such candidate genes, of potential clinical interest, are provided. We interpret these results in the framework of a meta‐analysis of previous investigations by others and ourselves and of existing clinical knowledge on the behavior of human tumors. The collective data show that metastases resemble their primary tumors but the signatures obtained in different studies are not sufficiently reproducible or informative to be prognostically useful, although they do give valuable insights into the pathogenesis and biology of human tumor metastasis. The findings indicate that the genetic program encoding metastasis is implemented progressively over time although, occasionally, this evolution can occur rapidly, early in the life of the neoplasm. The important clinical significance of this deduction is that, in most patients, early detection provides time for appropriate therapeutic intervention to be effective in obstructing metastasis. 相似文献