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131.
报道辐照氟银猪皮的制备、实验检测(弹性、创面粘附力和透水性测定,含银量测定)组织学检查细菌检测及抑菌试验研究,结果表明:辐照氟银猪皮除延伸度低于未辐照猪皮外,其撕裂强度、创面粘合力和透水性均与未辐照猪皮相似。组织学检查示:辐照氟银猪皮组织结构完整,表皮细胞部分空泡形成。组织细菌检测证明其无菌生长,达到无菌要求。抑菌试验证明对金黄色葡萄球菌、绿脓杆菌、大肠杆菌、变形杆菌、克雷伯氏菌均有极强的抑菌作用 相似文献
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133.
Many quantitative imaging protocols that make use of a metabolite-corrected arterial input function require the use of a mathematic model to describe the rate of metabolism of the radioligand. Commonly, parametric models are fit to metabolism data and then the fitted model is used to correct the plasma input function. (11)C-WAY 100635 is a rapidly metabolized radioligand used extensively in mapping the 5-hydroxytryptamine receptor 1A system. METHODS: To evaluate the adequacy of fit of 4 metabolite models, we examined data from 92 subjects who received an injection of (11)C-WAY 100635, were imaged with PET, and underwent measurement of total plasma concentration and metabolites. The performance of these models was assessed according to residual plots, as well as fit and information criteria. RESULTS: The study showed that the choice of model has a substantial effect on the resulting estimates of outcome measures. CONCLUSION: Among the models considered, the Hill model provides the best fit across all criteria. 相似文献
134.
458例尿路结石成分分析 总被引:4,自引:1,他引:3
目的 探讨西安地区尿路结石的成分状况,为临床防治提供帮助。方法对458例尿路结石标本进行化学成分测定,并结合临床资料进行比较。结果尿路结石男性发病多于女性,男、女比为2.1:1,20一50岁为高发年龄,上尿路结石明显多于下尿路结石,上、下尿路结石之比为10.5:1。结石成分以混合结石占多数,为325例(71%),其中以草酸钙,磷酸钙与尿酸的混合结石为主。对比混合性结石及单纯性结石发现,各种成分所占比例基本一致。结论结石成分分析对于了解结石成因、预防结石形成和复发具有重要的意义。 相似文献
135.
目的探讨在肝肥大-萎缩征中肥大肝叶内胆管结石的处理方法。方法回顾性分析我科1990年6月~2004年12月收治的103例肥大肝叶内胆管结石病人的临床资料,总结其手术治疗的原则和方法。结果全体病例均经手术治愈,术后残石率17.5%,效果优良率83.7%。结论肥大肝叶内的胆管结石,手术难度大,应根据病情选择手术方式,既要遵循肝胆管结石的治疗原则,又要保护赖以生存的肥大肝叶(段)。 相似文献
136.
目的探讨益肝灵对肾缺血再灌注损伤的保护作用。方法建立肾缺血再灌注模型,大鼠右肾切除,左侧肾蒂夹闭45min后再灌60min。用益肝灵预防性治疗,检测并比较肾组织及血清中MDA及SOD的活性变化。结果益肝灵能明显押制缺血再灌所致的血及肾组织中MDA的升高和SOD的活性降低。结论益肝灵对肾缺血再灌注损伤具有保护作用。 相似文献
137.
Growth hormone effects on hypertrophic scar formation: a randomized controlled trial of 62 burned children 总被引:3,自引:0,他引:3
Gisele V. de Oliveira MD ; Arthur P. Sanford MD ; Kevin D. Murphy MD ; Hermes M. de Oliveira MD ; Judy P. Wilkins RGN ; Xiaowu Wu MD ; Hal K. Hawkins MD PhD ; Gregory Kitten PhD ; David L. Chinkes PhD ; Robert E. Barrow PhD ; David N. Herndon MD 《Wound repair and regeneration》2004,12(4):404-411
The hypercatabolism after massive pediatric burns has been effectively treated with recombinant human growth hormone, an anabolic agent that stimulates protein synthesis and abrogates growth arrest. While experimental studies have shown increased potential for fibrosis induced by growth hormone therapy, adverse effects on human scars have not been investigated. Our aim was to evaluate hypertrophic scar formation in 62 patients randomized to receive injections of 0.05 mg/kg/day of recombinant human growth hormone or placebo, from discharge until 1 year after burn. Scar scales were used to evaluate scar-severity at discharge, 6, 9, 12, and 18-24 months after burn, by three observers blinded to treatment. Computer-assisted planimetry allowed quantification of percentage of hypertrophic scar formation. Types I and III collagens were localized and quantified in scars and normal skin of patients from both groups, using immunohistochemistry with confocal laser microscopy analysis. Insulin-like growth factor-1 blood levels helped assess compliance. Statistical analysis showed that scar hypertrophy significantly increased from 6 to 12 months after injury in both groups, while decreasing at 18-24 months postburn. Types I and III collagens were statistically increased in the reticular layer of scars from both groups when compared to paired normal skin. Insulin-like growth factor-1 was significantly increased in the recombinant human growth factor-treated group. No differences were seen when recombinant human growth factor and control groups were compared using the scar scales, planimetry, or immunohistochemistry. We concluded that recombinant human growth hormone therapy did not adversely affect scar formation and should not contraindicate the administration of recombinant human growth hormone as a therapeutic approach to severely burned children. 相似文献
138.
139.
血液透析是治疗急慢性肾衰竭的有效替代疗法之一。自20世纪60年代在我国开展以来,越来越多的肾病患者生命得以延续,血液透析人群亦呈逐年递增之势,值得注意的是,受疾病本身及透析合并症的影响,患者普遍存在较为严重的心理问题,如焦虑、忧郁、沮丧甚至绝望,不良的情绪可引发免疫力的下降,不仅不利于配合治疗,还严重影响了其生活质量。针对这些问题,我们经过分析研究,对在我院进行血液透析的患者进行了针对性的心理护理。现报告如下。 相似文献
140.
Disposition of tacrolimus in isolated perfused rat liver: influence of troleandomycin, cyclosporine, and gg918. 总被引:4,自引:0,他引:4
The disposition of tacrolimus and the influence of cyclosporine, troleandomycin, and GF120918 (GG918, or N-[4-[2-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolinyl)-ethyl]-phenyl]-9,10-dihydro-5-methoxy-9-oxo-4-acridine carboxamine) on its hepatic disposition were examined in the isolated perfused rat liver. Livers from groups of rats were perfused in a recirculatory manner following a bolus dose of tacrolimus (100 microg), a substrate for P-glycoprotein (P-gp) and CYP3A, or with felodipine (200 microg), a substrate only for CYP3A. Perfusions of each substrate were also examined in groups of rats in the presence of the inhibitors: troleandomycin (20 microM, CYP3A inhibitor), GG918 (1 microM, P-gp inhibitor), or cyclosporine (10 microM, CYP3A and P-gp inhibitor). In all experiments, perfusate and bile were collected for 60 min. Tacrolimus, felodipine, and their primary metabolites were determined in perfusate and bile by liquid chromatography/tandem mass spectrometry. The area under the curve (AUC) from 0 to 30 min was determined. For the dual CYP3A and P-gp substrate, tacrolimus, AUC +/- S.D. was decreased from control (2,260 +/- 430 ng. min/ml) by GG918 (1,730 +/- 270 ng. min/ml, P < 0.05) and was increased by troleandomycin (5,200 +/- 2,470 ng. min/ml, P < 0.05) and cyclosporine (4,390 +/- 2,080 ng. min/ml, P < 0.05). For the exclusive CYP3A substrate, felodipine, AUC was unchanged from control by GG918 but increased by troleandomycin and cyclosporine. It is concluded that GG918 increased the hepatic exposure of tacrolimus by inhibiting the canalicular P-gp transport, whereas GG918 has no effect on hepatic disposition of felodipine. These results support our hypothesis that the hepatic metabolic clearance of a dual substrate will be increased by inhibiting the efflux transporter. 相似文献