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排序方式: 共有1069条查询结果,搜索用时 31 毫秒
1.
Ngai-Yin Chan Chi-Chung Choy Ho-Chuen Yuen Hoi-Fan Chow Ho-Fai Fong 《The Canadian journal of cardiology》2019,35(4):396-404
Background
Persistent iatrogenic atrial septal defect (iASD) is a common but poorly characterized complication after cryoballoon (CB) pulmonary vein isolation (PVI) procedures. We therefore investigate its prevalence, evolution, risk factors, and clinical outcomes in a prospective longitudinal study.Methods
A total of 108 patients (41 women, mean age 57 ± 11.3) underwent CB PVI for AF. Serial transesophageal echocardiography (TEE) was performed 9 months and then annually until 6 years after the procedure to study the characteristics of persistent iASD.Results
Persistent iASD occurred in 33 (30.6%) patients 9 months after CB PVI. Spontaneous closure of iASD was found in 6 (22.2%) and 3 (15.8%) patients 2 and 3 years after the procedures, respectively. No spontaneous closure was observed on 4, 5, and 6-year TEE follow-up. The projected long-term persistence rate of iASD after CB PVI was therefore 20% (30.6% × 0.778 × 0.842). Using multivariate logistic regression, a higher number of cryoapplications (≥ 2 minutes) was the only independent predictor of persistent iASD 9 months after CB PVI (odds ratio [OR] 1.207; 95% confidence interval [CI], 1.033-1.411, P = 0.018). Two (1.9%) patients with significantly larger iASD size than the others (long diameter 12.6 ± 0.8 vs 3.7 ± 1.5 mm, P < 0.001; short diameter 10.9 ± 0.2 vs 3 ± 1.1 mm, P < 0.001) required percutaneous closure because of exertional dyspnea and right ventricular enlargement. Over 129.7 patient-years follow-up, during which iASD persisted, there was no occurrence of neurologic events.Conclusions
Approximately one fifth of patients undergoing CB PVI will have permanently persistent iASD. Patients with defect sizes of greater than 10 mm may need percutaneous closure due to significant left-to-right shunting. 相似文献2.
Min Deng Xian Jun Zeng Lai-Chang He Jason C.S. Leung Anthony W.L. Kwok James F. Griffith Timothy Kwok Ping Chung Leung Yì Xiáng J. Wáng 《Journal of clinical densitometry》2019,22(3):409-419
This study aims to evaluate endplate/cortex fracture (ECF)-based method for detecting osteoporotic vertebral fracture (VF) in elderly Chinese population (age ≥ 65 years). The radiographs of 1954 elderly Chinese men (mean: 72.3 years) and 1953 elderly Chinese women (mean: 72.5 years) were evaluated according to Genant's morphometrical vertebral deformity (VD) severity criteria, as well as identified VF according to ECF without necessary requirement of VD. According to ECF, grade-1, -2, and -3 VF prevalence was 1.89%, 1.74%, and 2.25% in men, and 3.33%, 3.07%, and 5.89% in women, respectively. In men and women, 15.7% (35 of 223) and 34.5% (48 of 139) of vertebrae with VD grade-1 deformity were ECF(+, with fracture), respectively. In men and women, 89.7% (35 of 39) and 66.7% (48 of 72) of vertebrae with ECF grade-1 fracture had VD grade-1 deformity. For grade-1 change, ECF(+) subjects tended to have a lower BMD than the VD(+) subjects. In subjects with VD grade-2 deformity, those who were also EC (+) tended to have a lower BMD than those were ECF(?). In all grades, VD(?) and ECF(?) subjects tended to have highest BMD, whereas VD(+) and ECF(+) subjects tended to have lowest BMD. ECF may be more specific for assessing mild VF than the criteria based on vertebral deformity. 相似文献
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Hong-Sheng Zhang Qian Liu Chun-Mei Piao Yan Zhu Qiang-Qiang Li Jie Du Hong Gu 《The Canadian journal of cardiology》2019,35(12):1851-1856
BackgroundThe relationship between clinical outcomes and gene mutations in Chinese pediatric patients with idiopathic and heritable pulmonary arterial hypertension (PAH) is unclear.MethodsWe retrospectively studied the clinical characteristics and outcomes of pediatric patients who visited Beijing Anzhen Hospital from September 2008 to December 2018.ResultsEighty-two pediatric patients were included. Forty-two gene mutations were identified in 41 patients (50%), including 25 mutations in BMPR2, 5 mutations in ACVRL1, 3 mutations each in ABCA3 and NOTCH3, 2 mutations each in KCNK3 and HTR2B, 1 mutation in ENG, and 1 mutation in EIF2AK4. The mean age at diagnosis of PAH was 86.4 ± 55.1 months. Forty-eight patients (twenty-eight mutation carriers) underwent cardiac catheterization examinations, with acute vasodilator testing performed simultaneously. Results showed that mutation carriers demonstrated a higher pulmonary vascular resistance index (P = 0.037). Patients with gene mutations responded poorly to vasodilators (P = 0.001). The 1-, 2-, and 3-year survival rates of mutation noncarriers were 95.1%, 87.8%, and 82.5% respectively; while for mutation carriers, the proportions were 86.6% (P = 0.216), 63.8% (P = 0.021), and 52.2% (P = 0.010), respectively. Cardiac index was an independent predictor of death (P = 0.005; odds ratio [OR] 2.16, 95% confidence interval [CI] 1.258-3.704), as well as RAP (P = 0.01; OR 1.26, 95% CI 1.056-1.503).ConclusionsIn our cohort of Chinese pediatric patients, those with an identified gene mutation demonstrated worse clinical outcomes. Therefore, early gene screening for pediatric patients with idiopathic and heritable PAH is recommended, and more aggressive treatment for mutation carriers may be advisable. 相似文献
4.
目的 比较接受巴塞罗那临床肝癌分期系统(BCLC)或香港的分期系统(HKLC)推荐治疗方案对肝细胞肝癌(HCC)患者生存率的影响。方法 回顾性分析436例初治肝癌患者的临床资料,根据HKLC和BCLC进行肿瘤分期,按是否最终接受两个分期系统推荐的治疗方案分组。比较患者是否接受BCLC或HKLC分期推荐方案治疗对生存率的影响,并评估拒绝BCLC或HKLC推荐方案对预后可能产生的影响。 结果 接受BCLC推荐治疗方案的患者5年生存率显著高于拒绝推荐治疗方案的患者(48% vs. 30%, P<0.001)。与拒绝推荐治疗方案的患者相比,接受HKLC推荐治疗方案的患者亦有较高的5年生存率(41% vs. 29%, P<0.001)。对BCLC和HKLC交叉亚组分析,BCLC-B/HKLC-Ⅰ+Ⅱa+Ⅱb、BCLC-B/HKLC-Ⅲa+Ⅲb和BCLC-C/HKLC-Ⅲa+Ⅲb亚组中,接受手术切除的HCC患者显著高于接受TACE、索拉非尼或最佳支持治疗的患者5年生存率均较高(均P<0.05)。 结论 接受BCLC和HKLC分期系统推荐治疗方案可以提高HCC患者的存活率,但对于中晚期肝癌患者指导作用减弱。部分BCLC-B/HKLC-Ⅰ+Ⅱa+Ⅱb、BCLC-B/HKLC-Ⅲa+Ⅲb和BCLC-C/HKLC-Ⅲa+Ⅲb的患者通过积极的根治性治疗可以获得更好的生存。 相似文献
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V.H.F. Lee J. Seong S.M. Yoon T.C.L. Wong B. Wang J.L. Zhang C.L. Chiang P.P.Y. Ho L.A. Dawson 《Clinical oncology (Royal College of Radiologists (Great Britain))》2019,31(8):560-569
Hepatocellular carcinoma (HCC) is a common malignancy worldwide, although its aetiologies vary significantly between the East and the West. About a half of HCC cases present with advanced unresectable HCC at the time of diagnosis, leading to a worse prognosis. Over the past 20 years, the treatment paradigm for advanced unresectable HCC has shifted from an entirely palliative approach to a multidisciplinary treatment, with continuous reassessment and possible repeat treatment attributed to the advent of novel and improved local, regional and systemic therapeutic options, contributed by both the East and the West. An individualised treatment plan should be determined for each patient, as there can be substantial differences in the decision-making and treatment response to the same treatment for different patients and different patient populations. This review provides a summary of the recent advances in management and compares Eastern and Western strategies for HCC. 相似文献
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