全文获取类型
收费全文 | 387219篇 |
免费 | 21813篇 |
国内免费 | 13781篇 |
专业分类
耳鼻咽喉 | 3646篇 |
儿科学 | 9422篇 |
妇产科学 | 4899篇 |
基础医学 | 38055篇 |
口腔科学 | 5388篇 |
临床医学 | 38391篇 |
内科学 | 59052篇 |
皮肤病学 | 3332篇 |
神经病学 | 25635篇 |
特种医学 | 17602篇 |
外国民族医学 | 85篇 |
外科学 | 50950篇 |
综合类 | 43479篇 |
现状与发展 | 57篇 |
一般理论 | 15篇 |
预防医学 | 34915篇 |
眼科学 | 7562篇 |
药学 | 31846篇 |
221篇 | |
中国医学 | 15482篇 |
肿瘤学 | 32779篇 |
出版年
2024年 | 752篇 |
2023年 | 3064篇 |
2022年 | 7903篇 |
2021年 | 10461篇 |
2020年 | 8217篇 |
2019年 | 6492篇 |
2018年 | 28367篇 |
2017年 | 23863篇 |
2016年 | 25672篇 |
2015年 | 11078篇 |
2014年 | 13098篇 |
2013年 | 13411篇 |
2012年 | 25000篇 |
2011年 | 40139篇 |
2010年 | 32671篇 |
2009年 | 23095篇 |
2008年 | 32842篇 |
2007年 | 34505篇 |
2006年 | 12781篇 |
2005年 | 12767篇 |
2004年 | 10919篇 |
2003年 | 11352篇 |
2002年 | 8295篇 |
2001年 | 4779篇 |
2000年 | 4136篇 |
1999年 | 3278篇 |
1998年 | 1955篇 |
1997年 | 1871篇 |
1996年 | 1409篇 |
1995年 | 1293篇 |
1994年 | 1065篇 |
1993年 | 647篇 |
1992年 | 803篇 |
1991年 | 683篇 |
1990年 | 687篇 |
1989年 | 539篇 |
1988年 | 464篇 |
1987年 | 408篇 |
1986年 | 320篇 |
1985年 | 257篇 |
1984年 | 156篇 |
1983年 | 131篇 |
1982年 | 83篇 |
1981年 | 73篇 |
1980年 | 80篇 |
1979年 | 81篇 |
1976年 | 57篇 |
1974年 | 66篇 |
1938年 | 60篇 |
1932年 | 60篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Wang Tao Liang Zhihou Sun Shenggang Cao Xuebing Peng Hai Cao Fei Liu Hongjin Tong E-tang 《华中科技大学学报(医学英德文版)》2003,23(2):145-147
Summary To investigate the distribution of possible novel mutations from parkin gene in variant subset of patients with Parkinson’s
disease (PD) in China and explore whether parkin gene plays an important role in the pathogenesis of PD, 70 patients were
divided into early-onset group and late-onset group; 70 healthy subjects were included as controls. Genomic DNA from 70 normal
controls and from those of PD patients were extracted from peripheral blood leukocytes by using standard procedures. Mutations
of parkin gene (exon 1–12) in all the subjects were screened by PCR-single strand conformation polymorphism (SSCP), and further
sequencing was performed in the samples with abnormal SSCP results, in order to confirm the mutation and its location. A new
missense mutation Gly284Arg in a patient and 3 abnormal bands in SSCP electrophoresis from samples of another 3 patients were
found. All the DNA variants were sourced from the samples of the patients with early-onset PD. It was concluded that Parkin
point mutation also partially contributes to the development of early-onset Parkinson’s disease in Chinese.
WANG Tao, male, born in 1961, Associate Professor
This work was supported by grants from the key program of the special scientific project of Scientific & Technologic Agency
of Hubei Province (Serial No. 2001AA308B01) and the Hygienic Research Project of Hygienic Agency of Hubei province (Serial
No. WJ 01529). 相似文献
992.
Adult-to-adult living donor liver transplantation using extended right lobe grafts. 总被引:11,自引:0,他引:11
下载免费PDF全文
![点击此处可从《Annals of surgery》网站下载免费的PDF全文](/ch/ext_images/free.gif)
C M Lo S T Fan C L Liu W I Wei R J Lo C L Lai J K Chan I O Ng A Fung J Wong 《Annals of surgery》1997,226(3):261-270
OBJECTIVE: The authors report their experience with living donor liver transplantation (LDLT) using extended right lobe grafts for adult patients under high-urgency situations. SUMMARY BACKGROUND DATA: The efficacy of LDLT in the treatment of children has been established. The major limitation of adult-to-adult LDLT is the adequacy of the graft size. A left lobe graft from a relatively small volunteer donor will not meet the metabolic demand of a larger recipient. METHODS: From May 1996 to November 1996, seven LDLTs, using extended right lobe grafts, were performed under high-urgency situations. All recipients were in intensive care units before transplantation with five having acute renal failure, three on mechanical ventilation, and all with hepatic encephalopathy. The median body weight for the donors and recipients was 58 kg (range, 41-84 kg) and 65 kg (range, 53-90 kg), respectively. The body weights of four donors were less than those of the corresponding recipients, and the lowest donor-to-recipient body weight ratio was 0.62:1. The extended right lobe graft was chosen because the left lobe volume was <40% of the ideal liver mass of the recipient. RESULTS: Median blood loss for the donors was 900 mL (range, 700-1600 mL) and hospital stay was 19 days (range, 8-22 days). Homologous blood transfusion was not required. Two donors had complications (one incisional hernia and one bile duct stricture) requiring reoperation after discharge. All were well with normal liver function 5 to 10 months after surgery. The graft weight ranged from 490 g to 1140 g. All grafts showed immediate function with normalization of prothrombin time and recovery of conscious state of the recipients. There was no vascular complication, but six recipients required reoperation. One recipient died of systemic candidiasis 16 days after transplantation and 6 (86%) were alive with the original graft at a median follow-up of 6.5 months (range, 5-10 months). CONCLUSIONS: When performed by a team with experience in hepatectomy and transplantation, LDLT, using an extended right lobe graft, can achieve superior results. The technique extends the success of LDLT from pediatric recipients to adult recipients and opens a new donor pool for adults to receive a timely graft of adequate function. 相似文献
993.
994.
David A Grimes J David Grimes Lem Racacho Kylie A Scoggan Fabin Han Betty Anne Schwarz John Woulfe Dennise Bulman 《Movement disorders》2002,17(6):1205-1212
The identification of rare, large families with Parkinson's disease (PD) has provided important clues that have contributed to our understanding of this complex disorder. We have identified a large French-Canadian kindred that spans five generations consisting of more than 90 individuals. A total of 65 individuals now have been examined, had venous blood drawn, and DNA extracted. Two-point and multipoint linkage analysis was performed to assess linkage to known PD genes or loci. Within the third and fourth generations of this family there are 10 living, plus 3 deceased members with well-documented levodopa responsive parkinsonism. Autopsy results on 1 member demonstrated the loss of pigmented neurons in the substantia nigra and the presence of alpha-synuclein positive Lewy bodies. Four of the PD patients have prominent postural and kinetic tremors that preceded their parkinsonism by up to 10 years. Two other individuals within the family have prominent isolated postural and kinetic tremors without parkinsonism. The alpha-synuclein(4q21.3-23), Parkin(6q25.2-27), PARK3 (2p13), PARK4, and ubiquitin carboxy terminal hydrolase-L1 (4p14-16.3) and PARK6 and PARK7 (1p35-36) loci were excluded in this kindred using closely linked markers. The clinical and pathological features of this family are consistent with the diagnosis of PD. This family further demonstrates the known genetic heterogeneity in PD and is large enough that a genome-wide screen has been undertaken in an effort to identify a novel PD gene. 相似文献
995.
大鼠肝小肠联合移植模型的建立 总被引:1,自引:0,他引:1
孙晓毅 《中华器官移植杂志》1997,18(4):194-195
本文报告一种封闭群大鼠进行的肝小肠联合移植模型。术中供体肝与小肠整块游离和灌注,分开切取。供肝原位、供肠异位移植于受体大鼠。主要血管用Kamada袖套法吻合,正式实验21次,3天以上存活率为43%。结果表明:减少手术时间和简化操作技术是提高成功率的关键因素和基本原则。 相似文献
996.
A case of a paraffinoma in the urinary bladder is presented. Plain radiography and intravenous urography showed a low attenuation filling defect in the urinary bladder, and CT demonstrated a lobulated fat-attenuation mass floating in the urinary bladder. 相似文献
997.
Atsushi Ota Nobuyasu Kano Hiroshi Kusanagi Shigetoshi Yamada Arty Garg 《Journal of hepato-biliary-pancreatic sciences》2003,10(2):172-175
Our basic techniques for the management of difficult cases of laparoscopic cholecystectomy (LC) are presented in this article. If access to Calot's triangle cannot be gained safely, dissection should be started at the fundus or body of the gallbladder (GB), rather than the neck (fundus-first method). In cases with a short and wide cystic duct, a transfixing suture should be applied for ligation instead of clipping. EndoGIA is useful for ligating and transecting this case to avoid a subsequent stricture caused by normal method of ligation. Intraoperative cholangiography should be performed near the neck of the GB in cases in which orientation is lost during dissection. More dissection should be performed in the direction of the junction of the bile ducts after orientation is regained. In cases with GB filled with stones accompanied by severe fibrosis, part of the GB is incised to remove the stones and expose the lumen of the GB. Confluence stones can be removed by placing an incision on the GB side of the junction of the duct. The incised part is closed with suture. A cystic tube (C-tube) is placed in the common bile duct through the cystic duct for decompression. In more difficult cases in which dissection cannot be started safely at any location, the body and the fundus of the GB are excised, and a drain is placed at the neck of the GB. Dissection can be carried out from the main surgeon's or the assistant's side depending on the situation, and cooperation between the two surgeons is mandatory to achieve safe LC in difficult cases. When performing the LC, one must have a low threshold for converting to open surgery if injuries cannot be managed safely. 相似文献
998.
目的 研究巢湖水有机提取物致突变性。方法 单细胞凝胶电泳技术测定鱼红细胞DNA损伤效应。结果 巢湖源水引起慧星细胞的百分率最高 (5 7.2 5 % ) ,滤前水最低 (2 7.6 3% ) ,出厂水经过二次加氯后慧星细胞的百分率有所上升 (4 4 .0 0 % )。结论 巢湖源水具有潜在致突变性 ,经混凝、活性炭吸附及沉淀处理后其DNA损伤作用有所下降 ,但氯化消毒可增加水中有机提取物的DNA损伤作用。 相似文献
999.
1000.
TuberculosisandSchistosomiasisarethemajorcontagiousdiseaseswhicharethemostdangeroustothepeople’shealth Inordertogetridofthem ,wemustlookforamoreusefulvaccine Bythetech niquesofmolecularbiology ,2 6 0 0 0DaGlutathionStransferase (GST) genewasclonedintotheE coli MycobacteriumtransferringandexpressionvectorpBCG 2 0 0 0totransformittoMycobacteriumsmeg matismc2 15 5 (MS)andBCGseparatelyinordertoconstructrMS Sj2 6GSTvaccineandrBCG Sj2 6GSTvaccine Inthisstudy ,theBALB/cmicewereimmu niz… 相似文献