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排序方式: 共有183条查询结果,搜索用时 15 毫秒
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Gilles G. Lestringant M.D. Khalil Qayed M.D. Benedict Blayney M.R.C.G.P. 《International journal of dermatology》1991,30(2):127-129
ABSTRACT: The authors reviewed the causative agents for tinea capitis in United Arab Emirates nationals attending Tawam Hospital, Al Ain, between 1981 and 1988. Microsporum canis was the most prevalent organism isolated. Oral griseofulvin remained the treatment of choice. The addition of isotretinoin appeared promising in the chronic inflammatory forms. 相似文献
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Magnuson JE; Brown ML; Hauser MF; Berquist TH; Fitzgerald RH Jr; Klee GG 《Radiology》1988,168(1):235-239
When infection of prosthetic orthopedic implants is suspected, optimal management requires accurate confirmation or exclusion of infection. The authors retrospectively studied 98 patients with possible infection who underwent scanning with indium-111-labeled white blood cells (WBCs) and subsequently underwent surgery within 14 days. At surgery, 50 patients had infections, as determined by means of culture or histologic results. The diagnostic accuracy of In-111 scanning was compared with that of plain radiography, arthrography, three-phase bone scanning, and various clinical and laboratory findings classically associated with infection. Positive findings on In-111 WBC scans and elevated erythrocyte sedimentation rates were found to be the most predictive variables in the diagnosis of septic prostheses (P less than or equal to .001 and P less than or equal to .002, respectively). Likelihood ratio analysis more clearly demonstrated the superiority of In-111 WBC scanning, with positive and negative scans yielding likelihood ratios of 5.0 and 0.16, respectively. 相似文献
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The ligand for CD40 (CD40L) is a protein which is expressed on CD4 T cells
following their activation: CD40-CD40L interactions are absolutely required
for the induction of T cell-dependent antibody responses, yet little is
known about the mechanisms whereby CD40L+ primary T cells activate naive B
cells, since the protein is only transiently expressed and is rapidly
down-regulated following T cell-B cell contact. We show here, using a
variety of assays, that co- stimulation of primary murine T cells via CD3
and CD28 stabilizes the expression of the CD40L protein. Firstly, T cells
stimulated in this manner express higher levels of CD40L when activated in
the presence of B cells, compared to CD3-activated T cells. Secondly, the
CD40L expressed on CD28-co-stimulated T cells is more resistant to B cell-
induced down-regulation. Finally, CD3/CD28-preactivated, rested T cells
re-express higher levels of CD40L more rapidly following re-stimulation via
CD3 than T cells preactivated via CD3 alone. CD3/CD28-preactivated T cells,
but not CD3-activated cells, are competent to induce DNA synthesis in naive
B cells, and this requires re-stimulation via CD3 and prolonged ligation of
CD40. These data therefore reinforce the concept that naive T cells need to
be activated initially by cognate interaction with B7-bearing
antigen-presenting cells (such as dendritic cells), before becoming
competent helper effector cells capable of driving B cells into
proliferation via a CD40-dependent pathway.
相似文献
28.
Digital imaging of the chest 总被引:4,自引:0,他引:4
Fraser RG; Sanders C; Barnes GT; MacMahon H; Giger ML; Doi K; Templeton AW; Cox GG; Dwyer SJ d; Merritt CR 《Radiology》1989,171(2):297-307
During the past several years, image acquisition in nuclear medicine, computed tomography, ultrasonography, subtraction angiography, and magnetic resonance has been by digitization. Despite these advances, research in the development of digital imaging in conventional radiography has lagged behind. Although studies with a variety of digital techniques have been carried out on several fronts, we still do not possess a method that has captured the imagination of the majority of radiologists and other physicians to a point where it could replace conventional screen-film imaging. This article reviews the current status and general principles of the technology, focusing on the four digital radiographic techniques that have shown the greatest promise - film digitization, an image intensifier - based system, photostimulable phosphor plates, and a scanned projection system. The physical aspects of each of the four systems and the clinical results that have been reported to date, as well as the advantages and disadvantages of each system, are presented. 相似文献
29.
Background: The use of ozone therapy in the treatment of dental caries is equivocal. The aim of this study was to use an in vitro model to determine the effects of prior ozone application to dentine on biofilm formation and to measure any associated reduction in bacteria viability. Methods: Twenty dentine discs were bonded to the bases of 5 mL polycarbonate screw top vials. Ten dentine discs were infused with ozone for 40 seconds, 10 samples remained untreated as a control. The vials were filled with nutrient medium, sterilized and placed into the outflow from a continuous chemostat culture of Streptococcus mutans and Lactobacillus acidophilus for four weeks. At the conclusion of the experiment bacterial growth was monitored by taking optical density readings of the growth medium in each vial and the outer surface of the dentine specimens were examined by scanning electron microscopy as shown by SEM analysis. Results: Ozone infusion prevented biofilm formation on all the treated samples while there was substantial biofilm present on the control specimens. While the average optical density of the control specimens was almost twice that of the ozone infused dentine (0.710 for the control with a SD of 0.288 and 0.446 for the ozonated samples with a SD of 0.371), the results were not significant (p > 0.05). Conclusions: This preliminary study has shown that the infusion of ozone into non‐carious dentine prevented biofilm formation in vitro from S. mutans and L. acidophilus over a four‐week period. The possibility exists that ozone treatment may alter the surface wettability of dentine through reaction with organic constituents. 相似文献
30.
Prostaglandin E2 (PGE2) is produced by activated platelets and by several other cells, including capillary endothelial cells. PGE2 exerts a dual effect on platelet aggregation: inhibitory, at high, supraphysiologic concentrations, and potentiating, at low concentrations. No information exists on the biochemical mechanisms through which PGE2 exerts its proaggregatory effect on human platelets. We have evaluated the activity of PGE2 on human platelets and have analyzed the second messenger pathways involved. PGE2 (5 to 500 nmol/L) significantly enhanced aggregation induced by subthreshold concentrations of U46619, thrombin, adenosine diphosphate (ADP), and phorbol 12-myristate 13-acetate (PMA) without simultaneously increasing calcium transients. At a high concentration (50 mumol/L), PGE2 inhibited both aggregation and calcium movements. PGE2 (5 to 500 nmol/L) significantly enhanced secretion of beta-thromboglobulin (beta TG) and adenosine triphosphate from U46619- and ADP-stimulated platelets, but it did not affect platelet shape change. PGE2 also increased the binding of radiolabeled fibrinogen to the platelet surface and increased the phosphorylation of the 47-kD protein in 32P- labeled platelets stimulated with subthreshold doses of U46619. Finally, the amplification of U46619-induced aggregation by PGE2 (500 nmol/L) was abolished by four different protein kinase C (PKC) inhibitors (calphostin C, staurosporine, H7, and TMB8). Our results suggest that PGE2 exerts its facilitating activity on agonist-induced platelet activation by priming PKC to activation by other agonists. PGE2 potentiates platelet activation at concentrations produced by activated platelets and may thus be of pathophysiologic relevance. 相似文献