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71.
①目的观察营养支持疗法辅助治疗慢性肺心病急性失代偿性呼吸衰竭的效果.②方法慢性肺心病急性失代偿性呼吸衰竭病人56例,随机分成两组,对照组(n=27)采用常规吸氧、抗生素、支气管解痉剂、祛痰剂、呼吸兴奋剂治疗;治疗组(n=29)在此基础上加用营养支持疗法复方氨基酸注射液250mL静滴,每日1次;100g/L脂肪乳注射液500mL静滴,每日1次,连用7~10d.比较两组病人的治疗效果及住院时间.③结果治疗组显效9例,有效16例;对照组显效4例,有效12例,两组疗效比较差异有显著意义(uc=2.09,P<0.05).治疗组住院时间为(20.3±4.2)d,对照组为(28.6±3.7)d,两组比较差异有显著意义(t=7.82,P<0.05).④结论营养疗法在慢性肺心病急性失代偿性呼吸衰竭治疗中有重要意义.  相似文献   
72.
BackgroundThe present article analyzes the association of the functional anterior cruciate ligament (ACL) status and the overall varus deformity and coronal tibiofemoral subluxation (CTFS) in varus OA of the knee.MethodsOne hundred consecutive knees with varus OA in 84 patients were prospectively included. Knees were divided into two groups, in accordance with the ACL status (functionally sufficient or insufficient). All included patients were potential candidates for unicompartmental knee arthroplasty with predominantly medial compartment OA. Knees with Kellgren/Lawrence ≥ grade 3 in the lateral compartment were excluded leaving 79 knees to be included in this study. Mechanical varus deformity and CTFS were evaluated on AP radiographs and valgus stress radiographs, and compared between the two groups.ResultsKnees with a functionally insufficient ACL had significantly more varus deformity on hip-to-ankle AP standing radiographs (P = .001) and on valgus stress radiographs (P = .017). CTFS on AP standing radiographs was significantly higher (P = .045) in knees with a functionally insufficient ACL. Seventy-three percent (8/11) of the ACL-insufficient knees had a varus deformity of ≥10° and 64% (7/11) of ACL-insufficient knees had CTFS ≥ 6mm. By contrast, only one patient (2%, 1/41) with an insufficient ACL had< 10° varus deformity and a CTFS of < 6mm.ConclusionFunctional ACL insufficiency in osteoarthritic varus knees is associated with greater varus deformity and more advanced CTFS. Seventy-three percent of ACL-insufficient knees had a varus deformity of ≥10° and 64% of ACL-insufficient knees a CTFS of ≥ 6mm. In the work-up for medial unicompartmental knee arthroplasty, functional ACL insufficiency is likely in knees with varus deformity of ≥10° and CTFS of ≥ 6mm.  相似文献   
73.
目的 观察公民逝世后器官捐献原位肝移植术后早期肝功能不全(early allograft dysfunction,EAD)的发生情况,探讨早期肝功能不全的危险因素。方法 回顾性分析2017年1月至2019年12月间我院65例行肝移植供、受体资料。根据术后情况将患者分为EAD组(n=29)及非EAD组(n=35)。对相关因素先进行单因素分析,然后将统计学差异的因素进行多因素Logistic回归模型分析。结果 65例原位肝移植患者术后早期肝功能不全的患者有29例,发生率为44.6%。单因素分析显示EAD组与非EAD组供体血清钠[(157.53±21.71)mmol/L vs(146.06±15.24)mmol/L,P=0.019]、热缺血时间[(21.6±6.5)min vs(10.6±4.3)min,P=0.016]、冷缺血时间[(8.3±1.2)h vs(5.4±1.2)h,P=0.012]、ICU住院时间[(78.1±19.5)h vs(49.7±17.6)h,P=0.007]及受体的无肝期时间[(98.3±16.3)h vs(66.0±17.6)h,P=0.037]差异均有统计学意义。多因素Logistic回归分析结果显示影响术后早期肝功能不全的独立危险因素为供体血清钠水平(OR 18.372,95%CI 1.846~24.173,P=0.019)及热缺血时间(OR 8.105,95%CI 1.513~37.205,P=0.013)。结论 供体血清钠水平及热缺血时间是公民逝世后器官原位肝移植术后EAD的独立危险因素。  相似文献   
74.
目的 探讨滑膜软骨瘤病的临床、病理与X线联系及诊断价值.方法 回顾性分析了17例滑膜软骨瘤病的临床、病理及X线表现.结果 本病好发于下肢大关节,多为单关节.膝关节10例(双侧2例)、肩关节3例、髋关节、肘关节、腕关节、指掌关节各1例.主要临床表现:关节肿痛、弹响(6例),绞锁(3例),触及可活动或不活动性硬块(9例).X线特点:在关节内及其周围见数目、大小、密度、形态不一的钙化或骨化游离体.结论 正确判断和认识关节内游离体来源与发展的病理变化及X线表现对诊断本病有较重要的价值.  相似文献   
75.
    
Zusammenfassung An frontalen Paraffinschnitten durch das Corpus callosum von 36 Säuglingen, Kindern und Erwachsenen wurden die postnatalen Veränderungen der Neuroglia untersucht. Dabei wurde festgestellt: 1. Im 4. Monat der postnatalen Entwicklung beginnt eine starke Vermehrung der Gliazellen. Ihre Anzahl pro Volumeneinheit steigt innerhalb von 2 Monaten auf etwa das 5fache des Wertes bei der Geburt. Nach dem 2. Lebensjahr nimmt die Zelldichte wieder ab. Diese Abnahme ist durch die Volumenzunahme des Fasermaterials zu erklären. 2. Die ersten Markscheiden werden im Alter von 41/2 Monaten sichtbar. In den folgenden Monaten nimmt ihre Zahl schnell zu. Das Dickenwachstum erfolgt langsam und in unterschiedlichem Maße. Das Auftreten der Markscheiden geht mit cytologischen Veränderungen der Gliazellen einher.Die postnatalen Veränderungen der Glia des Balkens werden mit den Verhältnissen in der Pyramide des Menschen und im Balken der Katze verglichen.
Postnatal changes of neuroglia in the corpus callosum of man
Summary In frontal sections through the corpus callosum of 36 human brains of various ages the postnatal development of the neuroglia has been investigated. It has been found: 1. That during the 4th month of postnatal life a rapid increase in the number of glial cells begins. Within the next two months the number of glial cells increases up to 5 times that found in the newborn. Later, the number of glial cells decreases again until in the second year after birth final values are reached. The decrease is due to an increase in volume of fibrous material. 2. That the first myelin sheaths are visible at an age of 41/2 months. During the following months their number increases quickly. In addition, there is a slow but irregular increase in the diameter of the myelin sheaths. 3. The appearence of the myelin sheaths is accompanied by cytological alterations of the glial cells.The postnatal changes of the neuroglia in the corpus callosum of man are compared with those in the pyramid of the human brain and in the corpus callosum of the cat.
Herrn Prof. Dr. Dr. E. Horstmann zum 60. Geburtstag gewidmet.  相似文献   
76.
复方黄芪袋泡饮改善慢性冠脉供血不足的研究   总被引:1,自引:0,他引:1  
复方黄芪袋泡饮改善慢性冠脉供血不足的研究刘志泉*陈跃*李岩飞*丁煜*为寻找一种比传统扩血管药物更为有效的中西药复方制剂以改善冠脉血供,降低心绞痛和心肌梗塞的发生率,我们依据中西药理论,结合现代血液流变学和微循环的科研成果,研制了以黄芪、阿司匹林为主要...  相似文献   
77.
The velo-cardio-facial syndrome (VCFS), caused by a submicroscopic deletion of chromosome 22q11, is the most common syndrome that has palatal anomalies as a major feature. A possible strategy for early detection of VCFS is routine screening for 22q11 deletions in all infants with cleft palate (CP). The purpose of this study was to evaluate whether this strategy is preferable to testing on clinical suspicion. At the Nijmegen Cleft Palate Craniofacial Center, 58 new patients with overt CP were routinely tested, using fluorescence in situ hybridization (FISH), for a 22q11 deletion. One deletion was identified in a newborn girl with an overt CP who was clinically not suspected of having VCFS. Based on this study (n = 45) and the literature (n = 54), the prevalence of 22q11 deletions among children with CP, but without any other symptoms of VCFS, is estimated to be one in 99. We take the view that this figure is rather low and that early discovery will rarely have significant clinical or genetic consequences. Because CP patients remain under medical attention, almost all of the infants with isolated CP and VCFS will be recognized as having the syndrome at a later age when additional features have developed. Therefore, we conclude that routine FISH testing for 22q11 deletions in infants with overt CP is not indicated, provided clinical follow-up is guaranteed.  相似文献   
78.
The role of leukocytes and cytokines in ovarian physiology isnow established, although the function of each cell type andcytokine remains to be determined in detail. Current knowledgeof these effects on follicle development, ovulation, luteinizationand luteotrophic process and luteolysis is reviewed. It is possiblethat further research will help to unravel some of the clinicalmysteries in ovarian function, including polycystic ovary syndrome,premature menopause, ovulatory disorders, and luteal phase defect.Furthermore, the increasing use of cytokines and their antagonistsin clinical practice may have significant effects upon reproductivefunction.  相似文献   
79.
Summary 15 biopsies of dilated and hypertrophied human left ventricles in mitral insufficient hearts were morphometrically investigated. On light and electron microscopical level the results were compared with those received from normally loaded human left ventricles and from hypertrophied human left ventricles found in hearts with aortic valve disease. The results demonstrate alterations when compared with the results from normally loaded left ventricles. The differences between normally loaded and volume loaded left ventricles are smaller than those in pressure loaded left ventricles from aortic valve diseased hearts.This work was supported gratefully by the Deutsche Forschungsgemeinschaft, SFB 104  相似文献   
80.
目的:探讨脑干听觉诱发电位(BAEP)在椎基底动脉供血不足(VBI)诊断中的意义。方法:对109例VBI患者做常规BAEP检查,并对其结果按年龄、病程进行分析。结果:109例中异常81例(743%),异常表现为各主波的潜伏期和波间期延长。其中病程<2年者异常率为406%(13/32例),2~5年者为878%(36/41),>5年者为889%(32/36)。结论:VBI患者的BAEP异常率有随病程延长而增高的倾向。BAEP对VBI缓解期病例的诊断有一定参考意义。  相似文献   
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