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Rosenberg ZS; Jahss MH; Noto AM; Shereff MJ; Cheung Y; Frey CC; Norman A 《Radiology》1988,167(2):489-493
Computed tomography (CT) was performed in 42 patients with 49 clinically suspected tears of the posterior tibial tendon. Twenty-eight of the 49 suspected tears were subsequently surgically explored and repaired. Three patterns of tendon abnormalities were recognized on CT scans: type I-intact, hypertrophied, heterogeneous tendon; type II-attenuated tendon; and type III-absence of a portion of a tendon. Types I and II correlated with partial rupture seen during surgery, and type III correlated with complete rupture of the tendon. CT findings were accurate in 96% of the patients who underwent surgery. In four cases (14%), tendon rupture was seen on CT scans, but the extent of the injury was underestimated and the rupture was misclassified. Reactive periostitis of the distal tibia was seen in 71% of diseased tendons and may represent an important factor in the diagnosis of tendon rupture. 相似文献
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Peroneus quartus muscle: MR imaging features 总被引:2,自引:0,他引:2
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二氢青蒿素的变旋作用与差向异构体转化研究 总被引:5,自引:0,他引:5
二氢青蒿素在极性溶媒中,其旋光度随时间而变化,可达一恒定值。高效液相色谱测定表明,在溶液中,该物质有一自β差向异构体向α型转化的动力学过程,此过程与旋光度的变化相对应,其转化速率常数随溶剂、温度而异,酸具催化作用。这一现象的本质是半缩醛的变旋作用。 相似文献
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拉米夫定(lamivudine)抗乙型肝炎病毒治疗中耐药突变发生率高,文献报道在拉米夫定治疗1,2,3,4,5a时分别为14%,38%,49%,66%,69%.耐药突变可导致血清HBVDNA水平阳转或明显上升,肝功能严重受损,甚至病情恶化死亡.关于拉米夫定抗乙型肝炎病毒治疗中耐药突变的后续治疗目前国内外尚无统一用药方案,单药治疗(如:继续使用拉米夫定、阿德福韦、恩替卡韦)在临床使用中已经取得了一定疗效,联合抗病毒治疗和中医药治疗是今后研究的方向. 相似文献
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Imaging cortical association tracts in the human brain using diffusion-tensor-based axonal tracking. 总被引:21,自引:0,他引:21
Susumu Mori Walter E Kaufmann Christos Davatzikos Bram Stieltjes Laura Amodei Kim Fredericksen Godfrey D Pearlson Elias R Melhem Meiyappan Solaiyappan Gerald V Raymond Hugo W Moser Peter C M van Zijl 《Magnetic resonance in medicine》2002,47(2):215-223
Diffusion-tensor fiber tracking was used to identify the cores of several long-association fibers, including the anterior (ATR) and posterior (PTR) thalamic radiations, and the uncinate (UNC), superior longitudinal (SLF), inferior longitudinal (ILF), and inferior fronto-occipital (IFO) fasciculi. Tracking results were compared to existing anatomical knowledge, and showed good qualitative agreement. Guidelines were developed to reproducibly track these fibers in vivo. The interindividual variability of these reconstructions was assessed in a common spatial reference frame (Talairach space) using probabilistic mapping. As a first illustration of this technical capability, a reduction in brain connectivity in a patient with a childhood neurodegenerative disease (X-linked adrenoleukodystrophy) was demonstrated. 相似文献
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James R. Cerhan Anne J. Novak Zachary S. Fredericksen Alice H. Wang Mark Liebow Timothy G. Call Ahmet Dogan Thomas E. Witzig Stephen M. Ansell Thomas M. Habermann Neil E. Kay Susan L. Slager 《British journal of haematology》2009,145(5):614-623
Germline mutations in complement genes have been associated with susceptibility to infections and autoimmune diseases, conditions that are associated with non-Hodgkin lymphoma (NHL) risk. To test the hypothesis that common genetic variation in complement genes affect risk of NHL, we genotyped 167 single nucleotide polymorphisms (SNPs) from 31 genes in 441 NHL cases and 475 controls. Principal components (PC) and haplotype analyses were used for gene-level tests of NHL risk, while individual SNPs were modelled as having a log-additive effect. In gene level PC analyses, C2 ( P = 0·023), C5 ( P = 0·0032) and C9 ( P = 0·020) were associated with NHL risk; haplotype analyses showed similar results, as well as a haplotype association for C7 ( P = 0·046). When all four genes were considered simultaneously, only C5 and C9 remained significant ( P < 0·05). In SNP level results from these genes, 10 SNPs had a P < 0·05. However, after correcting for multiple testing, only the C5 SNPs rs7026551 ( q = 0·015; OR = 1·54, 95% CI 1·21–1·95) and rs2416810 ( q = 0·015; OR = 1·57; 95% CI 1·22–2·01), and the C9 SNP rs187875 ( q = 0·015; OR = 0·68; 95% 0·56–0·84) remained noteworthy. Associations were similar for the common NHL subtypes. In summary, we provide evidence for a role of genetic variation in complement genes, particularly C5 and C9 , and NHL risk. 相似文献
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目的 :寻找具有正性肌力活性的化合物。方法 :根据文献报道的二氢喹啉酮类正性肌力药物的结构特点 ,设计、合成了其类似物。以苯胺为起始原料经多步合成 ,对所得化合物用离体豚鼠心脏与主动脉观察了心肌收缩力、扩血管作用及心率。结果 :合成了 1 0个 6 ( 4 酰基 1 哌嗪乙酰氨基 ) 3 ,4 二氢 2 ( 1H) 喹啉酮类化合物 ( 4a~ 4j) ,均为未见文献报道的化合物。结论 :初步药理试验表明 ,化合物 ( 4h)显示了正性肌力及扩血管活性。 相似文献