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1.
On April 20, 2018, the Kween District Health Office in Kween District, Uganda reported 7 suspected cases of human anthrax. A team from the Uganda Ministry of Health and partners investigated and identified 49 cases, 3 confirmed and 46 suspected; no deaths were reported. Multiple exposures from handling the carcass of a cow that had died suddenly were significantly associated with cutaneous anthrax, whereas eating meat from that cow was associated with gastrointestinal anthrax. Eating undercooked meat was significantly associated with gastrointestinal anthrax, but boiling the meat for >60 minutes was protective. We recommended providing postexposure antimicrobial prophylaxis for all exposed persons, vaccinating healthy livestock in the area, educating farmers to safely dispose of animal carcasses, and avoiding handling or eating meat from livestock that died of unknown causes.  相似文献   
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《Vaccine》2016,34(21):2430-2436
In a Phase 1 trial, we evaluated the safety of AERAS-402, an adenovirus 35-vectored TB vaccine candidate expressing 3 Mycobacterium tuberculosis (Mtb) immunodominant antigens, in subjects with and without latent Mtb infection. HIV-negative, BCG-vaccinated Kenyan adults without evidence of tuberculosis, 10 QuantiFERON®-TB Gold In-Tube test (QFT-G)(−) and 10 QFT-G(+), were randomized 4:1 to receive AERAS-402 or placebo as two doses, on Days 0 and 56, with follow up to Day 182. There were no deaths, serious adverse events or withdrawals. For 1 AERAS-402 QFT-G(−) and 1 AERAS-402 QFT-G(+) subject, there were 3 self-limiting severe AEs of injection site pain: 1 after the first vaccination and 1 after each vaccination, respectively. Two additional severe AEs considered vaccine-related were reported after the first vaccination in AERAS-402 QFT-G(+) subjects: elevated blood creatine phosphokinase and neutropenia, the latter slowly improving but remaining abnormal until study end. AERAS-402 was not detected in urine or throat cultures for any subject. In intracellular cytokine staining studies, curtailed by technical issues, we saw modest CD4+ and CD8+ T cell responses to Mtb Ag85A/b peptide pools among both QFT-G(−) and (+) subjects, with trends in the CD4+ T cells suggestive of boosting after the second vaccine dose, slightly more so in QFT-G(+) subjects. CD4+ and CD8+ responses to Mtb antigen TB10.4 were minimal. Increases in Adenovirus 35 neutralizing antibodies from screening to end of study, seen in 50% of AERAS-402 recipients, were mostly minimal. This small study confirms acceptable safety and tolerability profiles for AERAS-402, in line with other Phase 1 studies of AERAS-402, now to include QFT-G(+) subjects.  相似文献   
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目的 了解宁夏2019-2020年分离的炭疽芽胞杆菌菌株致病力及基因分型特征,为宁夏皮肤炭疽疫情判定与分子溯源提供实验室依据。方法 收集2019-2020年宁夏各地区分离的炭疽芽胞杆菌,对其进行毒力鉴定,并运用MLVA-15和canSNP分型技术进行基因分型研究。结果 2019-2020年宁夏分离到的炭疽芽胞杆菌均为强毒株,MLVA-15分型为同一种群,canSNP分型为A.Br.001/002组。结论 2019-2020年宁夏分离到的炭疽芽胞杆菌致病力较强,且菌株呈现相同的基因分型特征,提示菌株间存在流行病学关联。此研究结果填补了宁夏炭疽芽胞杆菌实验室检测中菌株致病力及基因分型的空白。  相似文献   
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目的探讨枯草杆菌二联活菌肠溶胶囊对经肝动脉化疗栓塞术(TACE)术后不良反应及并发症的防治作用。方法选取2012年1月-2013年12月大连大学附属中山医院收治的择期进行TACE的肝细胞癌患者239例,随机分为试验组(n=111)与对照组(n=128)。其中试验组于术前3 d给予口服枯草杆菌二联活菌肠溶胶囊,对照组服用外形相同的安慰剂,比较2组TACE术后不良反应、并发症发生率及血氨水平。计量资料组间比较采用独立样本t检验,计数资料组间比较采用χ2检验。结果试验组患者发热、腹胀、便秘等不良反应发生率显著低于对照组,差异均有统计学意义(t值分别为2.728、2.561、2.026,P值均0.05);试验组患者肝脓肿、肠梗阻、自发性腹膜炎、肝性脑病等术后并发症的发生率亦显著低于对照组,差异均有统计学意义(t值分别为1.969、2.312、2.987、2.826,P值均0.05);经治疗后,与对照组相比,试验组患者血氨水平较低,差异具有统计学意义(t=1.97,P0.05)。结论枯草杆菌二联活菌肠溶胶囊作为新型活菌制剂,能够降低TACE术后患者腹部不适及血氨水平,并能够减少肝脓肿等严重并发症的发生,但相关机制尚需进一步研究。  相似文献   
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目的了解医院重症监护室(ICU)与非ICU主要革兰阴性(G-)杆菌的分布及耐药性,为临床合理使用抗菌药物提供依据。方法对某院2011—2013年住院患者送检标本中培养分离的G-菌标本来源及耐药性进行统计分析,比较ICU与非ICU的差异。结果 25 153份标本共分离G-菌3 875株,分离率15.41%;其中ICU1 121份标本中分离G-菌527株,分离率47.01%,非ICU24 032份标本分离G-菌3 348株,分离率13.93%,两者比较差异有统计学意义(χ2=899.32,P0.001)。大肠埃希菌和肺炎克雷伯菌产超广谱β-内酰胺酶(ESBLs)菌株检出率:ICU分别为56.00%(28/50)、70.65%(65/92),非ICU分别为52.81%(517/979)和40.37%(241/597)。ICU中铜绿假单胞菌、鲍曼不动杆菌、大肠埃希菌、肺炎克雷伯菌对亚胺培南的耐药率分别为36.59%、88.54%、10.00%、10.87%,均高于非ICU同类菌的耐药率,分别为20.21%、61.15%、1.74%、2.85%。结论 ICU主要G-杆菌的耐药率高于非ICU,且以多重耐药的非发酵菌为主。临床治疗应区别对待,以减少耐药菌的产生。  相似文献   
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The neutralization of toxins is considered essential for protection against lethal infection with Bacillus anthracis (BA), a select agent and bioterrorism threat. However, toxin‐neutralizing activity alone would not be expected to provide sterile immunity. Therefore, we hypothesized that the development of an adaptive immune response against BA is required for bacterial clearance. We found that human monocyte‐derived dendritic cells (hDCs) kill germinated BA bacilli, but not nongerminated BA spores. hDCs produce IL‐1β, IL‐6, IL‐12, and IL‐23, and these cytokines are differentially regulated by germination‐proficient versus germination‐deficient BA spores. Moreover, the IL‐23 response to BA spores is regulated by IL‐1R‐mediated signaling. hDCs infected with germinating BA spores stimulated autologous CD4+ T cells to secrete IL‐17A and IFN‐γ in a contact‐dependent and antigen‐specific manner. The T‐cell response to BA spores was not recapitulated by hDCs infected with germination‐deficient BA spores, implying that the germination of spores into replicating bacilli triggers the proinflammatory cytokine response in hDCs. Our results provide primary evidence that hDCs can generate a BA‐specific Th17 response, and help elucidate the mechanisms involved. These novel findings suggest that the IL‐23/Th17 axis is involved in the immune response to anthrax in humans.  相似文献   
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