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91.
G Schuler K L Peterson A Johnson G Francis G Dennish J Utley P O Daily W Ashburn J Ross 《Circulation》1979,59(6):1218-1231
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Human γ-aminobutyric acid type B receptors are differentially expressed and regulate inwardly rectifying K+ channels 下载免费PDF全文
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Visual estimation versus different quantitative coronary angiography methods to assess lesion severity in bifurcation lesions 下载免费PDF全文
Maik J. Grundeken MD PhD Carlos Collet MD Yuki Ishibashi MD PhD Philippe Généreux MD Takashi Muramatsu MD PhD Laura LaSalle MPH Aaron V. Kaplan MD Joanna J. Wykrzykowska MD PhD Marie‐angèle Morel BsC Jan G. Tijssen PhD Robbert J. de Winter MD PhD Yoshinobu Onuma MD PhD Martin B. Leon MD Patrick W. Serruys MD PhD 《Catheterization and cardiovascular interventions》2018,91(7):1263-1270
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Elisabeth Schuler Horst Urbach Andreas Schulze-Bonhage Julia Jacobs-LeVan 《Zeitschrift für Epileptologie》2016,29(3):168-172
We report the case of a 14-year-old male with a history of focal seizures since the age of six due to a focal cortical dysplasia located within the left frontal lobe. The patient’s seizures proved to be refractory to treatments with Oxcarbazepine, Lamotrigine, Valproate, and Clobazame. Because fMRI for language mapping suggested a close spatial relationship of the lesion and Broca’s area, invasive language mapping was performed using a subdural grid for direct cortical stimulation. This suggested a clear topographic distinction between the lesion and Broca’s area, finally enabling language retaining lesionectomy. This case illustrates some pitfalls of fMRI language mapping in preoperative workup for epilepsy surgery. 相似文献
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We investigated the efficacy of granisetron and dolasetron in preventing postoperative nausea and vomiting. Because the metabolism of the various antiemetic 5-hydroxytryptamine type 3 (5-HT3) antagonists involves different isoforms of the hepatic cytochrome P450 system, we examined the relationship between the clinical efficacy of these drugs and polymorphic cytochrome P450 2D6 (CYP2D6) genotype. This prospective, randomized, double-blind study involved 150 adult patients with a moderate to high risk for postoperative nausea and vomiting. All subjects received dexamethasone at induction of anesthesia followed by either 12.5 mg of dolasetron or 1 mg of granisetron. We analyzed the number of complete responders (no vomiting or rescue medication) during the first 24 hours after surgery. CYP2D6 genotyping was performed using a TaqMan real-time polymerase chain reaction. A complete response was more frequent in the granisetron group (54.7%) compared with the dolasetron group (38.7%, P < 0.05). In subjects receiving dolasetron, carriers of the duplication of the CYP2D6 allele predicting ultrarapid metabolizer status had more frequent vomiting episodes (P < 0.05) than patients in the granisetron group. It is postulated that the difference in the antiemetic efficacy between two investigated 5-HT3 receptor antagonists may be associated with differences in the carrier status for the duplication of the CYP2D6 allele. 相似文献
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Birkenfeld Andreas L.; Gollasch Maik; Gobel Ursula; Luft Friedrich C. 《Nephrology, dialysis, transplantation》2004,19(6):1643-1645
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NSF workshop report: Discovering general principles of nervous system organization by comparing brain maps across species 下载免费PDF全文
Georg F. Striedter T. Grant Belgard Chun‐Chun Chen Fred P. Davis Barbara L. Finlay Onur Güntürkün Melina E. Hale Julie A. Harris Erin E. Hecht Patrick R. Hof Hans A. Hofmann Linda Z. Holland Andrew N. Iwaniuk Erich D. Jarvis Harvey J. Karten Paul S. Katz William B. Kristan Eduardo R. Macagno Partha P. Mitra Leonid L. Moroz Todd M. Preuss Clifton W. Ragsdale Chet C. Sherwood Charles F. Stevens Maik C. Stüttgen Tadaharu Tsumoto Walter Wilczynski 《The Journal of comparative neurology》2014,522(7):1445-1453
Efforts to understand nervous system structure and function have received new impetus from the federal Brain Research through Advancing Innovative Neurotechnologies (BRAIN) Initiative. Comparative analyses can contribute to this effort by leading to the discovery of general principles of neural circuit design, information processing, and gene‐structure‐function relationships that are not apparent from studies on single species. We here propose to extend the comparative approach to nervous system ‘maps' comprising molecular, anatomical, and physiological data. This research will identify which neural features are likely to generalize across species, and which are unlikely to be broadly conserved. It will also suggest causal relationships between genes, development, adult anatomy, physiology, and, ultimately, behavior. These causal hypotheses can then be tested experimentally. Finally, insights from comparative research can inspire and guide technological development. To promote this research agenda, we recommend that teams of investigators coalesce around specific research questions and select a set of ‘reference species' to anchor their comparative analyses. These reference species should be chosen not just for practical advantages, but also with regard for their phylogenetic position, behavioral repertoire, well‐annotated genome, or other strategic reasons. We envision that the nervous systems of these reference species will be mapped in more detail than those of other species. The collected data may range from the molecular to the behavioral, depending on the research question. To integrate across levels of analysis and across species, standards for data collection, annotation, archiving, and distribution must be developed and respected. To that end, it will help to form networks or consortia of researchers and centers for science, technology, and education that focus on organized data collection, distribution, and training. These activities could be supported, at least in part, through existing mechanisms at NSF, NIH, and other agencies. It will also be important to develop new integrated software and database systems for cross‐species data analyses. Multidisciplinary efforts to develop such analytical tools should be supported financially. Finally, training opportunities should be created to stimulate multidisciplinary, integrative research into brain structure, function, and evolution. J. Comp. Neurol. 522:1445–1453, 2014. © 2014 Wiley Periodicals, Inc. 相似文献