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991.
Douglas K. Rex MD Amitabh Chak MD Rajeev Vasudeva MD Thomas Gross MD David Lieberman MD Ishan Bhattacharya MD Elizabeth Sack MD Maurits Wiersema MD Francis Farraye MD Michael Wallace MD Daniel Barrido MD Eileen Cravens MD Leonard Zeabart MD David Bjorkman MD Todd Lemmel MD Scott Buckley MD 《Gastrointestinal endoscopy》1999,49(6):727-730
992.
Prevalence and severity of urinary incontinence in older African American and Caucasian women. 总被引:4,自引:0,他引:4
N H Fultz A R Herzog T E Raghunathan R B Wallace A C Diokno 《The journals of gerontology. Series A, Biological sciences and medical sciences》1999,54(6):M299-M303
BACKGROUND: Few studies have investigated the prevalence and severity of urinary incontinence in older African American women. Comparisons of findings with those for older Caucasian women could provide important clues to the etiology of urinary incontinence and be used in planning screening programs and treatment services. METHODS: Data are from the first wave of the Asset and Health Dynamics Among the Oldest Old (AHEAD) study. A nationally representative sample of noninstitutionalized adults 70 years of age and older was interviewed. African Americans were oversampled to ensure that there would be enough minority respondents to compare findings across racial groups. RESULTS: A statistically significant relationship was found between race and urinary incontinence in the previous year: 23.02% of the Caucasian women reported incontinence, compared with 16.17% of the African American women. Other factors that appear to increase the likelihood of incontinence include education, age, functional impairment, sensory impairment, stroke, body mass, and reporting by a proxy. Race was not related to the severity (as measured by frequency) of urine loss among incontinent older women. CONCLUSION: This study identifies or confirms important risk factors for self-reported urinary incontinence in a national context, and suggests factors leading to protection from incontinence. Race is found to relate to incontinence, with older African American women reporting a lower prevalence. 相似文献
993.
Sanne A. Hoogenboom Candice W. Bolan Anthony Chuprin Maria T. Raimondo Jeanin E. van Hooft Michael B. Wallace Massimo Raimondo 《Pancreatology》2021,21(2):428-433
BackgroundThe prevalence of pancreatic ductal adenocarcinoma (PDAC) is on the rise, driven by factors such as aging and an increasing prevalence of obesity and diabetes mellitus. To improve the poor survival rate of PDAC, early detection is vital. Recently, pancreatic steatosis has gained novel interest as a risk factor for PDAC. This study aimed to investigate if pancreatic steatosis on computed tomography (CT) is an early imaging feature in patients with pre-diagnostic PDAC.MethodsA retrospective case-control study was performed. Patients diagnosed with PDAC (2010–2016) were reviewed for abdominal non-contrast CT-imaging 1 month-3 years prior to their diagnosis. Cases were matched 1:4 with controls based on age, gender and imaging date. Unenhanced CT-images were evaluated for pancreatic steatosis (pancreas-to-spleen ratio in Hounsfield Units <0.70) by a blinded radiologist and results were compared between cases and controls.ResultsIn total, 32 cases and 117 controls were included in the study with a comparable BMI (29.6 and 29.2 respectively, p = 0.723). Pancreatic steatosis was present in 71.9% of cases compared to 45.3% of controls (Odds ratio (OR) 3.09(1.32–7.24), p = 0.009). Adjusted for BMI and diabetes mellitus, pancreatic steatosis on CT remained a significant independent risk factor for PDAC (Adjusted OR 2.70(1.14–6.58), p = 0.037).ConclusionPancreatic steatosis measured on CT is independently associated with PDAC up to three years before the clinical diagnosis in overweight patients. If these data are confirmed, this novel imaging feature may be used to identify high-risk individuals and to stratify the risk of PDAC in individuals that already undergo PDAC screening. 相似文献
994.
995.
Induction and maintenance infliximab therapy for the treatment of moderate-to-severe Crohn's disease in children 总被引:16,自引:0,他引:16
Hyams J Crandall W Kugathasan S Griffiths A Olson A Johanns J Liu G Travers S Heuschkel R Markowitz J Cohen S Winter H Veereman-Wauters G Ferry G Baldassano R;REACH Study Group 《Gastroenterology》2007,132(3):863-73; quiz 1165-6
BACKGROUND AND AIMS: The REACH study evaluated the safety and efficacy of infliximab in children with moderately to severely active Crohn's disease. METHODS: Patients (n = 112) with a Pediatric Crohn's Disease Activity Index (PCDAI) score >30 received infliximab 5 mg/kg at weeks 0, 2, and 6. Patients responding to treatment at week 10 were randomized to infliximab 5 mg/kg every 8 or 12 weeks through week 46. A concurrent immunomodulator was required. Clinical response (decrease from baseline in the PCDAI score > or =15 points; total score < or =30) and clinical remission (PCDAI score < or =10 points) were evaluated at weeks 10, 30, and 54. RESULTS: At week 10, 99 of 112 (88.4%) patients responded to infliximab (95% confidence interval: [82.5%, 94.3%]) and 66 of 112 (58.9%) patients achieved clinical remission (95% confidence interval: [49.8%, 68.0%]). At week 54, 33 of 52 (63.5%) and 29 of 52 (55.8%) patients receiving infliximab every 8 weeks did not require dose adjustment and were in clinical response and clinical remission, respectively, compared with 17 of 51 (33.3%) and 12 of 51 (23.5%) patients receiving treatment every 12 weeks (P = .002 and P < .001, respectively). CONCLUSIONS: Pediatric patients responding to an induction regimen of infliximab were more likely to be in clinical response and remission at week 54 without dose adjustment when their maintenance therapy was given every 8 weeks rather than every 12 weeks. Allowing for dose intensification in the case of relapse, remission rates, but not response rates, at week 54 were superior with every 8-week dosing compared with every 12-week dosing. 相似文献
996.
Wallace LS DeVoe JE Rogers ES Malagon-Rogers M Fryer GE 《Journal of general internal medicine》2007,22(11):1538-1543
BACKGROUND Patients’ race and ethnicity play an important role in quality of and access to healthcare in the United States.
OBJECTIVES To examine the influence of ethnicity – Hispanic whites vs. non-Hispanic whites – on respondents’ self-reported interactions
with healthcare providers. To understand, among Hispanic whites, how demographic and socioeconomic characteristics impact
their interactions with healthcare providers.
DESIGN Cross-sectional analysis of the 2002 Medical Expenditure Panel Survey, a nationally representative survey on medical care
conducted by the Agency for Healthcare Research and Quality.
PARTICIPANTS Civilian, noninstitutionalized U.S. population aged ≥18 years who reported visiting a healthcare provider within the past
12 months prior to data collection.
RESULTS After controlling for several demographic and socioeconomic covariates, compared to non-Hispanic whites (reference group),
Hispanic whites who had visited a doctor’s office or clinic in the past 12 months were more likely to report that their healthcare
provider “always” listened to them [odds ratio (OR) = 1.36, 95% confidence interval (CI) 1.21–1.53], explained things so that
they understood (OR = 1.25, 95% CI 1.10–1.41), showed respect for what they had to say (OR = 1.52, 95% CI 1.35–1.72), and
spent enough time with them (OR = 1.22, 95% CI 1.08–1.38). However, Hispanics were less likely to indicate that their health
care provider “always” gave them control over treatment options (OR = 0.83, 95% CI 0.72–0.95) as compared to non-Hispanics.
Within the Hispanic population exclusively, age, place of residence, census region, health insurance status, and presence
of a usual source of care influenced self-reported interactions with healthcare providers.
CONCLUSION Hispanic white respondents were more likely to report that some aspects of provider–patient interactions were indicative of
high quality, whereas those related to decision-making autonomy were not. These somewhat paradoxical results should be examined
more fully in future research. 相似文献
997.
Travis R. Sexton Eric L. Wallace Amy Chen Richard J. Charnigo Hassan K. Reda Khaled M. Ziada John C. Gurley Susan S. Smyth 《Journal of thrombosis and thrombolysis》2016,41(3):384-393
Transcatheter aortic valve replacement (TAVR) has been increasingly used to treat patients with symptomatic aortic stenosis. Despite improvements in valve deployment, patients that have undergone TAVR are at high risk for major adverse events following the procedure. Blood cell numbers, platelet function, and biomarkers of systemic inflammation were analyzed in 58 patients undergoing TAVR with the Edward’s SAPIEN valve. Following valve deployment, platelet count and agonist-induced platelet activity declined and plasma markers of systemic inflammation (interleukin-6 and S100A8/A9) increased. Baseline platelet activity prior to TAVR correlated with perioperative changes plasma interleukin-6 levels. Moreover, perioperative changes in plasma inflammatory markers predicted the decline in platelet count in the days following the TAVR procedure. Additionally, a significant effect of gender on platelet count following TAVR and was observed. Finally, post-procedural mortality was associated with sustained thrombocytopenia after TAVR. Our findings suggest that TAVR elicits a thromboinflammatory state that may contribute to post-procedural thrombocytopenia. Importantly, our results add to the growing body of literature that suggests the thromboinflammatory changes that occur early after TAVR may predict long-term outcomes. 相似文献
998.
Cyclooxygenase 2 mediates post-inflammatory colonic secretory and barrier dysfunction 总被引:7,自引:0,他引:7
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BACKGROUND AND AIMS: The colonic epithelium plays a key role in host defence. During colitis, epithelial function is impaired, leading to elevated bacterial translocation and exacerbation of inflammation. We previously documented perturbation of epithelial function, in terms of secretion and as a barrier to bacterial translocation, that persisted long after resolution of a bout of colitis in the rat. The mechanisms underlying the epithelial dysfunction are not completely understood. METHODS: Given the ability of prostaglandin (PG) D2 to suppress colonic epithelial secretion, we investigated the potential roles of this eicosanoid and of cyclooxygenase 2 (COX-2) in mediating post-colitis epithelial secretory and barrier dysfunction. RESULTS: Six weeks after induction of colitis with trinitrobenzene sulphonic acid, there was marked elevated synthesis of PGD2 and elevated COX-2 expression. Selective COX-2 inhibition abolished the increase in PGD2 synthesis. Colonic chloride secretory responses (in vitro) were significantly diminished relative to those in controls, a defect that was reversed by pre-exposure to a selective COX-2 inhibitor (celecoxib) but not to a selective COX-1 inhibitor (SC-560). The hyporesponsiveness was mimicked by pre-exposure of normal colonic tissue to PGD2, but not to its metabolite, 15-deoxy-Delta(12-14)PGJ2. The post-colitis rats exhibited a 10-fold increase in bacterial colonisation of the colon, and >3-fold increase in bacterial translocation. Twice daily treatment for one week with a selective COX-2 inhibitor (rofecoxib) did not affect bacterial colonisation but abolished the increase in bacterial translocation. CONCLUSIONS: These studies demonstrate an important role for COX-2, possibly via generation of PGD2, in mediating the prolonged epithelial secretory and barrier dysfunction after a bout of colitis in the rat. 相似文献
999.
Diverse HIV-1 subtypes and clinical, laboratory and behavioral factors in a recently infected US military cohort 总被引:5,自引:0,他引:5
1000.
D. Isenberg J. Sturgess E. Allen C. Aranow A. Askanase B. Sang‐Cheol S. Bernatsky I. Bruce J. Buyon R. Cervera A. Clarke Mary Anne Dooley P. Fortin E. Ginzler D. Gladman J. Hanly M. Inanc S. Jacobsen D. Kamen M. Khamashta S. Lim S. Manzi O. Nived C. Peschken M. Petri K. Kalunian A. Rahman R. Ramsey‐Goldman J. Romero‐Diaz G. Ruiz‐Irastorza J. Sanchez‐Guerrero K. Steinsson G. Sturfelt M. Urowitz R. van Vollenhoven D. J. Wallace A. Zoma J. Merrill C. Gordon 《Arthritis care & research》2018,70(1):98-103