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排序方式: 共有2757条查询结果,搜索用时 578 毫秒
91.
Pierre Ct Hainan Yu Heather M. Shearer Kristi Randhawa Jessica J. Wong Silvano Mior Arthur Ameis Linda J. Carroll Margareta Nordin Sharanya Varatharajan Deborah Sutton Danielle Southerst Craig Jacobs Maja Stupar Anne Taylor‐Vaisey Douglas P. Gross Robert J. Brison Mike Paulden Carlo Ammendolia J. David Cassidy Patrick Loisel Shawn Marshall Richard N. Bohay John Stapleton Michel Lacerte 《European Journal of Pain》2019,23(6):1051-1070
92.
Atul Mehta David J. Kuter Sam S. Salek Nadia Belmatoug Bruno Bembi Jeremy Bright Stephan vom Dahl Federica Deodato Maja Di Rocco Ozlem Göker‐Alpan Derralynn A. Hughes Elena A. Lukina Maciej Machaczka Eugen Mengel Aabha Nagral Kimitoshi Nakamura Aya Narita Beatriz Oliveri Gregory Pastores Jordi Pérez‐López Uma Ramaswami Ida V. Schwartz Jeff Szer Neal J. Weinreb Ari Zimran 《Internal medicine journal》2019,49(5):578-591
93.
Maja Derlink Barbara Pipan Petra Pavlovčič Laura E. Jones Vladimir Meglič William O. C. Symondson Meta Virant-Doberlet 《Conservation Genetics Resources》2014,6(4):933-935
Eleven microsatellite markers were developed for the leafhoppers of the genus Aphrodes using shotgun pyrosequencing and will be used to study the genetic diversity, population structure and gene flow within and between species in this genus in order to assess their conservation status. The number of alleles per locus ranged from 3 to 10, while observed and expected heterozygosity values varied from 0.421–1.000 to 0.542–0.876, respectively. Cross-species amplification was successful among the four congeners. 相似文献
94.
Mller Petra Sell Christian Hadrys Thorsten Hedman Johannes Bredemeyer Steffi Laurent Francois-Xavier Roewer Lutz Achtruth Sabrina Sidstedt Maja Sijen Titia Trimborn Marc Weiler Natalie Willuweit Sascha Bastisch Ingo Parson Walther 《International journal of legal medicine》2020,134(1):185-198
International Journal of Legal Medicine - We present results from an inter-laboratory massively parallel sequencing (MPS) study in the framework of the SeqForSTRs project to evaluate forensically... 相似文献
95.
Anne-Laure Lapeyraque Nastya Kassir Yves Théorêt Maja Krajinovic Marie-José Clermont Catherine Litalien Véronique Phan 《Pediatric nephrology (Berlin, Germany)》2014,29(6):1081-1088
Background
The objectives of this study were to investigate pharmacokinetic and pharmacogenetic parameters during the conversion on a 1:1 (mg:mg) basis from a twice-daily (Prograf) to once-daily (Advagraf) tacrolimus formulation in pediatric kidney transplant recipients.Methods
Twenty-four-hour pharmacokinetic profiles were analyzed before and after conversion in 19 stable renal transplant recipients (age 7–19 years). Tacrolimus pharmacokinetic parameters [area under the concentration-time curve (AUC0–24), minimum whole-blood concentration (Cmin), maximum whole-blood concentration (Cmax), and time to achieve maximum whole-blood concentration (tmax)] were compared between Tac formulations and between CYP3A5 and MDR1 genotypes after dose normalization.Results
Both AUC0–24 and Cmin decreased after conversion (223.3 to 197.5 ng.h/ml and 6.5 to 5.6 ng/ml; p?=?0.03 and 0.01, respectively). However, the ratio of the least square means (LSM) for AUC0–24 was 90.8 %, with 90 % CI limits of 85.3 to 96.7 %, falling within bioequivalence limits. The CYP3A5 genotype influences the dose-normalized Cmin with the twice-daily formulation only.Conclusions
Both tacrolimus formulations are bioequivalent in pediatric renal recipients. However, we observed a decrease in AUC0–24 and Cmin after the conversion, requiring close pharmacokinetic monitoring during the conversion period. 相似文献96.
Nenad Filipović Sonja Grubišić Maja Jovanović Marija Dulović Ivanka Marković Olivera Klisurić Aleksandar Marinković Dragana Mitić Katarina Anđelković Tamara Todorović 《Chemical biology & drug design》2014,84(3):333-341
Novel Pd(II) complex with N‐heteroaromatic Schiff base ligand, derived from 8‐quinolinecarboxaldehyde (q8a) and ethyl hydrazinoacetate (haOEt), was synthesized and characterized by analytical and spectroscopy methods. The structure of novel complex, as well as structures of its quinoline and pyridine analogues, was optimized by density functional theory calculations, and theoretical data show good agreement with experimental results. A cytotoxic action of the complexes was evaluated on cultures of human promyelocytic leukemia (HL‐60), human glioma (U251), rat glioma (C6), and mouse fibrosarcoma (L929) cell lines. Among investigated compounds, only complexes with quinoline‐based ligands reduce the cell numbers in a dose‐dependent manner in investigated cell lines. The observed cytotoxic effect of two isomeric quinoline‐based complexes is predominantly mediated through the induction of apoptotic cell death in HL‐60 cell line. The cytotoxicity of most efficient novel Pd(II) complex is comparable to the activity of cisplatin, in all cell lines investigated. 相似文献
97.
98.
99.
Annette Zimpfer Stephanie Janke Maja Hühns Björn Schneider Günther Kundt Heike Zettl Ergin Kilic Matthias Maruschke Oliver W. Hakenberg Andreas Erbersdobler 《Pathology, research and practice》2014
Introduction
C-kit overexpression has previously been described in chromophobe renal cell carcinoma (cpRCC) and renal oncocytoma (RO). However, so far no KIT mutations have been found. The objective of our study was to analyse c-kit in a large cohort of renal tumors and to perform KIT mutation analysis in a subset cpRCC and RO cases with overexpression of c-kit.Materials and methods
We studied the immunohistochemical expression of c-kit on tissue microarrays containing formalin-fixed, paraffin-embedded samples of 948 patients with renal tumors. CpRCC and RO cases with c-kit overexpression (n = 23) were analyzed for KIT mutations in exons 9, 11, 13, 14, 15, and 17.Results
Expression of c-kit was found in 6/642 (0.9%) clear cell RCC, 3/154 (1.9%) papillary RCC, 54/69 (78.3%) cpRCC, 37/45 (82.2%) RO and 2/30 (6.7%) of other unclassified tumor types. In none of the RO and cpRCC cases analyzed, a KIT gene mutation was found.Conclusion
C-kit expression is found in the majority of cpRCC and RO, but these tumors do not harbor the usual c-kit activating mutations. This may have implications for the use of tyrosine kinase inhibitors in patients with advanced cpRCC and c-kit expression. 相似文献100.
Maja Wilhelmsen Ragnhild S?rensen H?if?dt Nils Kolstrup Knut Waterloo Martin Eisemann Richard Chenhall Mette Bech Ris?r 《Journal of medical Internet research》2014,16(9)