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91.
92.
Thellea K. Leveque Le Yu David C. Musch Ronald D. Chervin David N. Zacks 《Sleep & breathing》2007,11(4):253-257
Patients with obstructive sleep apnea (OSA), in comparison to controls, have increased levels of circulating epinephrine and
norepinephrine, both of which are risk factors for the development of central serous chorioretinopathy (CSCR). The aim of
this pilot study was to investigate the frequency of symptoms that suggest OSA in CSCR patients and normal controls. The Berlin
Questionnaire, a validated research tool to assess risk for OSA, was administered to 29 patients who met the criteria for
active, acute, non-steroid-induced CSCR and 29 controls matched for age and sex. In this retrospective case-controlled study,
the main outcome measure was increased risk for OSA. The mean age of the patients was 47.8 years (range 29–72) and the mean
age of controls was 47.3 years (range 25–70). Seventy-six percent (22) of both groups were men. Survey scores showed 58.6%
(17) of patients with CSCR to be at an increased risk for OSA compared to 31.0% (nine) of controls. A conditional logistic
regression analysis showed that the CSCR group had a higher proportion with an increased risk for OSA compared to the control
group (odds ratio=3.67; 95% CI: 1.02, 13.14; P = 0.046). Patients with CSCR may be more likely than other adults to have OSA, and screening for this sleep disorder should
be considered in this population. Further research is warranted to determine whether sleep apnea may contribute to the development
of CSCR, and to assess whether treatment of sleep apnea might offer a new therapeutic option for some patients with CSCR. 相似文献
93.
A passion for P450s (rememberances of the early history of research on cytochrome P450). 总被引:4,自引:0,他引:4
Ronald W Estabrook 《Drug metabolism and disposition》2003,31(12):1461-1473
Many members of the superfamily of hemeproteins, known as cytochrome P450 (P450 or CYP), are currently described in the literature (over 2000 at the date of this writing) [see Nelson, 2003 (http://drnelson.utmem.edu/CytochromeP450.html)]. In mammalian tissues, the P450s play central roles in drug and xenobiotic metabolism as well as steroid hormone synthesis, fat-soluble vitamin metabolism, and the conversion of polyunsaturated fatty acids to biologically active molecules. P450s also play a major role in plants by catalyzing the synthesis of a large number of secondary metabolites. Today we appreciate the unique oxygen chemistry catalyzed by the P450 enzymes as well as the dramatic effect of protein structural changes resulting in modifications of substrate specificity. Recent scientific advances have shown the importance of genetic differences (polymorphisms) in altering the physiological response of an animal to endo- and exo-biotic chemicals. In many instances these changes can be directly attributed to small differences in the amino acid sequence of a P450. The present article describes some of the early events associated with the establishment of the biological function of P450s. The 1950s and 1960s showed the transition of P450 from an unknown spectroscopic curiosity to the major player it now occupies in maintaining cellular homeostasis. The P450s are now recognized to occupy a great variety of phylogenetically distributed isoform activities. Much has been learned about the P450s, but much more remains as poorly understood. It has been almost 50 years since this class of unique proteins were discovered and their catalytic functions characterized. The present article describes the background and early history of research leading to our present knowledge of the cytochromes P450. Hopefully we will learn lessons from this history as we venture forward down the path of future scientific discovery. 相似文献
94.
George Karpati Djordje Ajdukovic Douglas Arnold Robert B. Gledhill Ronald Guttmann Paul Holland Penelope A. Koch Eric Shoubridge Desmond Spence Michel Vanasse Gordon V. Watters Michael Abrahamowicz Catherine Duff Ronald G. Worton 《Annals of neurology》1993,34(1):8-17
One biceps muscle of 8 patients with Duchenne muscular dystrophy was injected at 55 sites with a total of 55 million viable, purified, and contamination-free normal myoblasts (myoblast transfer). The other biceps of each patient was injected with a placebo to serve as a control. The procedure was blinded to the patients, parents, and investigators. Myoblasts derived from a biopsy specimen of the fathers were cultured and purified under strict conditions and carefully screened for microbial contamination. All patients received cyclophosphamide for immunosuppression for 6 or 12 months. No serious complications were observed after myoblast transfer, indicating that the procedure is safe. The overall therapeutic efficiency of myoblast transfer was poor as judged by the results in maximal voluntary force generation, dystrophin content of the muscle, magnetic resonance imaging of the muscle, and the lack of donor-derived DNA and dystrophin messenger RNA in the injected muscle. An improved efficiency of the take of myoblasts might be achieved by using younger cells and injecting the myoblasts with a myonecrotic agent (to increase the prevalence of regeneration) and a basal laminal fenestrating agent. 相似文献
95.
96.
Li Shihong Schöneich Christian Wilson George S. Borchardt Ronald T. 《Pharmaceutical research》1993,10(11):1572-1579
The effect of primary structure and external conditions on the oxidation of methionine to methionine sulfoxide by the ascorbate/Fe3+ system was studied in small model peptides. Degradation kinetics and yield of sulfoxide formation were dependent on the concentration of ascorbate and H+, with a maximum rate observed at pH 6–7. Phosphate buffer significantly accelerated the peptide degradation compared to Tris, HEPES, and MOPS buffers; however, the formation of sulfoxide was low. The oxidation could not be inhibited by the addition of EDTA. Other side products besides sulfoxide were observed, indicating the existence of various other pathways. The influence of methionine location at the C terminus, at the N terminus, and in the middle of the sequence was investigated. The presence of histidine in the sequence markedly increased the degradation rate as well as the sulfoxide production. The histidine catalysis of methionine oxidation occurred intramolecularly with a maximum enhancement of the oxidation rate and sulfoxide production when one residue was placed between the histidine and the methionine residue. 相似文献
97.
Richard B. Dewey Jr Surendra D. Rao Stephanie L. Holmburg Ronald G. Victor 《European journal of neurology》1998,5(6):593-599
Eight patients with parkinsonism who developed severe orthostatic sypotension, were treated with oral ergotamine/caffeine. Significant long-term improvement in standing systolic blood pressure and symptoms of syncope and light-headedness were observed in four of these patients. One patient in whom the drug was effective discontinued it because of nausea. Another lost benefit after 2 weeks of sucessful therapy. Significant supine systolic hypertension occureed in only one patient, which was easily managed by nifedipine given at night. Symptoms or signs of ergotism were not observed. Oral ergotamine/caffeine should be considered as a cost-effective teratment for refactory orthostatic hypotension in carefully selected patients with parkinsonism. 相似文献
98.
Buprenorphine, a partial mu-opioid receptor agonist, has been proposed as a treatment for cocaine abuse. However, studies
in animals have produced conflicting results on the nature of the interaction between buprenorphine and cocaine. In some studies,
buprenorphine attenuated the effects of cocaine and in others it enhanced them. The purpose of the present study was to evaluate
the interaction of buprenorphine and cocaine on the rotational behavior of the nigrally-lesioned rat. Both buprenorphine (0.003–0.1
mg/kg) and cocaine (1.0– 30 mg/kg) alone produced dose-dependent increases in rotational behavior. Buprenorphine produced
long-lasting turning with a peak at 60 min after administration, while cocaine produced turning that peaked immediately after
administration and lasted for about 2 h. To distinguish simple additivity from other possible outcomes, we determined the
relative potency of each drug alone, using a defined level of effect: 150 turns above the saline control in 4 h. This effect
was produced by 10.0 mg/kg cocaine alone and by 0.0175 mg/kg buprenorphine alone. Based on these results, fixed ratio combinations
were tested and the experimentally derived effects were compared to the theoretically additive values, using an isobolographic
analysis. The fixed ratio combinations of the two drugs tested produced turning greater than predicted from simple additivity.
This finding provides statistically-supported evidence for synergism between the actions of buprenorphine and cocaine.
Received: 28 January 1997 / Final version: 7 June 1997 相似文献
99.
Wong Joseph Kuu Wei-Youh Burke Ronald Johnson Robert Wood Ray W. 《Pharmaceutical research》1995,12(1):144-148
The primary objective of this work was to establish a method to simulate the plasma levels of cilastatin, a model drug, following an intravenous in-line delivery scheme. In-vivo data in dogs obtained from this work were used to demonstrate the validity of the proposed approach. The in-line drug delivery system consists of a drug containing device which is placed between a large volume parenteral and a patient. Numerous advantages have been identified for this automatic in-line reconstitution delivery system. The numerical convolution integral algorithm was used in this work to perform plasma profile simulation. The results indicated that the simulated cilastatin plasma profile following in-line delivery closely agreed with the in-vivo data. 相似文献
100.