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31.
术中超声引导放射性^125Ⅰ粒子组织间植入治疗局部晚期胰腺癌 总被引:1,自引:0,他引:1
目的 探讨超声引导下术中放射性^125Ⅰ粒子组织间种植治疗无法切除胰腺癌的可行性和疗效。方法 2002年4月~2005年2月,我院行开腹^125Ⅰ粒子植入治疗晚期胰腺癌21例。术前根据治疗计划,确定粒子活度和种植粒子个数,肿瘤匹配周边剂量为65~110Gy,每颗粒子活度为0.4~0.5mCi。超声引导下插入粒子种植针,Mick粒子植入器植入^125Ⅰ粒子,粒子植入数10~75颗。8例粒子植入前或后行胃肠或胆肠吻合术。2例术后行外放疗联合单药吉西他滨化疗。1例术前置入支架,1例术后置入支架。结果 15例腹痛中,14例术后1~3d疼痛即开始缓解,其中7例疼痛完全缓解,7例部分缓解,1例无效,有效率93.3%(14/15);除2例失访外,CR5例,PR7例,PD5例,NC2例。19例中位生存期5个月,1年生存率26.3%。1例出现乳糜漏,3例粒子移位到肝脏。无胰漏和胰腺炎等并发症。结论 放射性^125Ⅰ粒子组织间种植治疗胰腺癌具有安全、有效、创伤小和并发症发生率低等优点,是一种较好的补救治疗手段。 相似文献
32.
蝎毒多肽对大鼠纤溶系统的作用 总被引:1,自引:0,他引:1
从蝎毒中获取具有多种药理活性的肽类混合物(简称SVP),用下肢血管灌流和整体给药的动物模型,观察对血管灌流液内纤溶酶原激活物(PA)活性、血浆优球蛋白纤溶活性(EFA)、纤溶酶(PL)活性的影响。结果:1~20μg/ml灌流3min和0.8,1.6mg·kg-1ipSVP1h血浆中PA活性与对照组相比明显升高(P<0.05或P<0.01),这可能与血管内皮细胞释放PA活性增加有关。 相似文献
33.
The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease. 总被引:2,自引:0,他引:2
Cao Li Zhang Ting Xiao Qin Wang Ying Bai Li Lu Guo Qiang Ma Jian Fang Zhang Jing Ding Jian Qing Chen Sheng Di 《Movement disorders》2007,22(16):2439-2443
We conducted a case-control study to determine the prevalence of the LRRK2 Gly2385Arg variant in patients with Parkinson's disease in Han population in mainland China. Heterozygous LRRK2 Gly2385Arg variant was identified in 14 of 235 patients with Parkinson's disease (5.69%), but not in 214 unrelated healthy controls. Multivariate analysis indicated the frequency of Gly2385Arg variant in the female patients with early age at onset is higher than their male counterparts. The founder haplotype analysis showed the variant carriers shared the same founder. Clinically, the LRRK2 Gly2385Arg carriers presented with classical Parkinson's disease symptoms. Our study indicates that the LRRK2 Gly2385Arg variant is a potential ethnic-specific genetic risk factor of Parkinson's disease within Chinese Han ethnicity. 相似文献
34.
北京石景山地区孕妇女婴幼儿血铅动态研究 总被引:8,自引:2,他引:6
在严格的质量保证措施下,北京石景山地区270名孕妇及其婴儿进行了血铅的追瞎调查。结果显示:孕3月血铅水平为45.0μg/L,分娩前血铅水平为64.8μg/L,孕期血铅呈升高趋势,其中后3月升高明显,分娩前血铅约为孕3月血铅的1.5倍;脐带血铅水平为51.9μg/L,其中有10.4%的胎儿脐血铅高于100μg/L; 相似文献
35.
目的 建立检测人CEA的T7 RNA聚合酶催化的荧光扩增技术.方法 以亲和素作为连接分子,连接生物素化的检测抗体和生物素化的DNA,加入T7RNA聚合酶进行转录扩增反应,对生成的RNA产物进行荧光检测,并同时进行夹心ELISA方法检测人CEA.结果 成功的建立了检测人CEA的T7 RNA聚合酶催化的荧光扩增技术,其检测CEA的灵敏度达2×10 -3 ng/ml,比夹心EL ISA 方法灵敏度高125倍.结论 T7 RNA聚合酶催化的荧光扩增技术较夹心ELISA方法具有更高的敏感性,有可能作为一种新的检测方法用于临床的早期诊断. 相似文献
36.
37.
This apparatus is designed in accordance with the doctrine and principles of traditional Chinese medicine and based on the theory of meridian and specific massage procedure in conjunction with the "Information Theory" and electron utilizing technique. It utilizes a programmed induction "Special Wave" to stimulate a series of acupuncture points, combined with administration of western drugs from a regime of "General Attack" treatment on the gallbladder stones, to enhance their evacuation. By stimulating the specific acupuncture points with this apparatus through the action of "Special Wave" strong contraction of the gallbladder can be elicitated. Experiments on dogs showed that under such stimulation the intra-gallbladder pressure can be increased 26 times, producing a jet of bile flow which facilitates the expulsion and evacuation of stones in the gallbladder. Method of use: first place a conductive rubber pad on the acupuncture point to be stimulated, then use a hand-held electrode to massage-stimulate the meridian. It is carried out forward and backward along the direction of meridian. The whole procedure is carried out under direct visualization with the help of ultrasonic B-scan. When dilatation of the common bile duct is observed, the hand-help electrode is used to perform push-compress massage on the meridian, and acupuncture points making the stones enter the common bile duct B-scan give proper orientation for the manipulation. This method has been tested clinically on 410 patients with good results. The evacuation rate of the gallbladder stones was 92.7% with complete evacuation achieved in 17.3%.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
38.
39.
Functional tyrosine kinase inhibitor profiling: a generally applicable method points to a novel role of platelet-derived growth factor receptor-beta in tuberous sclerosis 总被引:1,自引:0,他引:1 下载免费PDF全文
Arbiser JL Govindarajan B Bai X Onda H Kazlauskas A Lim SD Amin MB Claesson-Welsh L 《The American journal of pathology》2002,161(3):781-786
A ubiquitous herpesvirus that establishes life-long infection, the Epstein-Barr virus (EBV) has yielded little insight into how a single agent in general accord with its host can produce diverse pathologies ranging from oral hairy leukoplakia to nasopharyngeal carcinoma, from infectious mononucleosis to Hodgkin's disease (HD) and Burkitt's lymphoma. Its pathogenesis is further confounded by the less than total association of virus with histologically similar tumors. In other viral systems, defective (interfering) viral genomes are known to modulate outcome of infection, with either ameliorating or intensifying effects on disease processes initiated by prototype strains. To ascertain whether defective EBV genomes are present in HD, we examined paraffin-embedded tissue from 56 HD cases whose EBV status was first determined by cytohybridization for nonpolyadenylated EBV RNAs (EBERs). Using both standard polymerase chain reaction (PCR) and PCR in situ hybridization, we successfully amplified sequences that span abnormally juxtaposed BamHI W and Z fragments characteristic of defective heterogeneous (het) EBV DNA from 10 of 32 (31%) EBER-positive tumors. Of 24 EBER-negative HD, 8 yielded PCR products indicating presence of het EBV DNA. Two of these contained defective EBV in the apparent absence of the prototype virus. Of the 42 tumors analyzed for defective EBV by both PCR techniques, there was concordance of results in 38 (90%). Detection of defective EBV genomes with the potential to disrupt viral gene regulation suggests one mechanism for pathogenic diversity that may also account for loss of prototypic EBV from individual tumor cells. 相似文献
40.
Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q 总被引:3,自引:0,他引:3
Vijay Tonk Herman E. Wyandt Peter Osella James Skare Bai Lin Wu Bassem Haddad Aubrey Milunsky 《Clinical genetics》1995,48(3):151-155
A 4-month-old child with multiple anomalies was determined to have an interstitial deletion of chromosome 15, i.e., del(15) (q12q14). The deletion appears not to be a typical deletion of 15q12 such as seen in Angelman and Prader-Willi syndromes, but appears to be more distal, involving either loss of all of 15q12 and part of 15q14, or part of 15q12 and most of 15q14. In either case, 15q13 is missing. Fluorescent in situ hybridization with probes for 15 centromere (D15Z), pericentromeric satellite sequences (D15Z1), and chromosome 15 painting probes shows the deleted chromosome to involve only 15 and no other acrocentric chromosome. Hybridization with probes for the AS and PWS loci (D15S11 and GABAB3, Oncor) show both sites to be intact in the deleted 15. The case is compared with two other reports with overlapping interstitial deletions of proximal 15q, neither of which shows typical features of Angelman or Prader-Willi syndromes. 相似文献