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21.
Christian A. Kühne C. Krueger M. Homann C. Mohr S. Ruchholtz 《Oral and maxillofacial surgery》2007,11(4):201-208
Objective
To minimize overall mortality and optimise reconstructive and cosmetic outcome in severely injured patients with maxillofacial injuries the interdisciplinary coordination of several surgical disciplines is required. It is still discussed controversy whether patients with maxillofacial fractures benefit from early fracture repair or if delayed operative management also yields in good results.Methods
Herein we analysed the data of 1252 severely injured patients between May 1998 through June 2002 in our trauma department regarding fractures of the maxillofacial region, injury severity, length of ICU stay and postoperative complications in patients with either early (within 72?hours) or delayed (>?3?days) facial fracture repair.Results
147 patients had severe facial fractures. Average age was 39.8 years (3–87 years), mean ICU was 25 (+/– 16) and the overall mortality 12% (n?=?18). The most common cause for the injuries were traffic accidents in 45%. 78 patients (53%) underwent surgical repair of the maxillofacial fractures; 18 patients had early fracture repair and 60 patients had delayed operative repair. We found 4 complications (22%) in the early repair group and 13 local complications (21%) in the group with delayed surgical repair.Conclusion
Delayed repair of maxillofacial injuries in severely injured patients is feasible and yields in good results compared to early fracture repair. 相似文献22.
Further characterization of factor VIII-deficient mice created by gene targeting: RNA and protein studies 总被引:6,自引:7,他引:6
Bi L; Sarkar R; Naas T; Lawler AM; Pain J; Shumaker SL; Bedian V; Kazazian HH Jr 《Blood》1996,88(9):3446-3450
23.
First pass metabolism of ethanol is strikingly influenced by the
speed of gastric emptying 总被引:2,自引:0,他引:2 下载免费PDF全文
C Oneta U Simanowski M Martinez A Allali-Hassani X Pares N Homann C Conradt R Waldherr W Fiehn C Coutelle H Seitz 《Gut》1998,43(5):612-619
Background—Ethanol undergoes a first passmetabolism (FPM) in the stomach and liver. Gastric FPM of ethanolprimarily depends on the activity of gastric alcohol dehydrogenase(ADH). In addition, the speed of gastric emptying (GE) may modulateboth gastric and hepatic FPM of ethanol.
Aims—To study the effect of modulation of GE onFPM of ethanol in the stomach and liver.
Methods—Sixteen volunteers (eight men andeight women) received ethanol (0.225 g/kg body weight) orally andintravenously, and the areas under the ethanol concentration timecurves were determined to calculate FPM of ethanol. In seven of thesesubjects, FPM of ethanol was measured after the intravenousadministration of 10 mg metoclopramide (MCP) and 20 mgN-butylscopolamine (NBS) in separate experiments to eitheraccelerate or delay GE. GE was monitored sonographically by integrationof the antral area of the stomach every five minutes for 90 minutesafter oral ethanol intake. In addition, gastric biopsy specimens weretaken to determine ADH activity and phenotype, as well as to evaluategastric histology. Blood was also drawn for ADH genotyping.
Results—GE time was significantly delayed by theadministration of NBS as compared with controls (p<0.0001) and ascompared with the administration of MCP (p<0.0001). This wasassociated with a significantly enhanced FPM of ethanol with NBScompared with MCP (p = 0.0004). A significant correlation was notedbetween GE time and FPM of ethanol (r = 0.43, p = 0.0407).Gastric ADH activity did not significantly correlate with FPM of ethanol.
Conclusion—FPM of ethanol is strikingly modulatedby the speed of GE. Delayed GE increases the time of exposure ofethanol to gastric ADH and may therefore increase gastric FPM ofethanol. In addition, hepatic FPM of ethanol may also be enhanced asthe result of slower absorption of ethanol from the small intestine. Thus a knowledge of GE time is a major prerequisite for studying FPM ofethanol in humans.
Aims—To study the effect of modulation of GE onFPM of ethanol in the stomach and liver.
Methods—Sixteen volunteers (eight men andeight women) received ethanol (0.225 g/kg body weight) orally andintravenously, and the areas under the ethanol concentration timecurves were determined to calculate FPM of ethanol. In seven of thesesubjects, FPM of ethanol was measured after the intravenousadministration of 10 mg metoclopramide (MCP) and 20 mgN-butylscopolamine (NBS) in separate experiments to eitheraccelerate or delay GE. GE was monitored sonographically by integrationof the antral area of the stomach every five minutes for 90 minutesafter oral ethanol intake. In addition, gastric biopsy specimens weretaken to determine ADH activity and phenotype, as well as to evaluategastric histology. Blood was also drawn for ADH genotyping.
Results—GE time was significantly delayed by theadministration of NBS as compared with controls (p<0.0001) and ascompared with the administration of MCP (p<0.0001). This wasassociated with a significantly enhanced FPM of ethanol with NBScompared with MCP (p = 0.0004). A significant correlation was notedbetween GE time and FPM of ethanol (r = 0.43, p = 0.0407).Gastric ADH activity did not significantly correlate with FPM of ethanol.
Conclusion—FPM of ethanol is strikingly modulatedby the speed of GE. Delayed GE increases the time of exposure ofethanol to gastric ADH and may therefore increase gastric FPM ofethanol. In addition, hepatic FPM of ethanol may also be enhanced asthe result of slower absorption of ethanol from the small intestine. Thus a knowledge of GE time is a major prerequisite for studying FPM ofethanol in humans.
Keywords:first pass metabolism of ethanol; gastric emptying; alcohol dehydrogenase; ethanol metabolism; stomach
相似文献24.
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27.
Adrien Daigeler Ludger Klein-Hitpass Ansgar Michael Chromik Oliver Müller Jörg Hauser Heinz-Herbert Homann Hans-Ulrich Steinau Marcus Lehnhardt 《BMC cancer》2008,8(1):313
Background
Doxorubicin is considered one of the most potent established chemotherapeutics in the treatment of liposarcoma; however, the response rates usually below 30%, are still disappointing. This study was performed to identify gene expression changes in liposarcoma after doxorubicin treatment. 相似文献28.
29.
Tang RB Wang HY Lu HY Xiong J Li HH Qiu XH Liu HQ 《第二军医大学学报》2005,26(8):880-880
There have been extensive observations that RNA containing repetitive elements accumulates in transformed cells and tumor tissues. In the present study, we first obtained result consistent with previous observations by in situ hybridization. 相似文献
30.
Janjaap van der Net Patrick van der Torre Raoul HH Engelbert Vivian Engelen Femke van Zon Tim Takken Paul JM Helders 《Pediatric rheumatology online journal》2008,6(1):2