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81.
发病72h内的急性缺血性脑梗死60例,分为2组。尼莫地平组30例(男性21例,女性9例;年龄59±s10a)。wk1.2给支持疗法(脱水剂,维生素C等)和尼莫地平2mg/d于5%葡萄糖液500ml内静脉滴注。wk3.4改用扩容、改善微循环,细胞活性药。wkl-4口服尼莫地平60mg.qn。对照组30例(男性23例,女性7例;年龄58±9a)。不给尼莫地平,其余同上。4wk后,前组神经功能缺损积分值较后组下降显著(P相似文献
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83.
α1-抗糜蛋白酶基因、早老素1基因
与阿尔茨海默病的相关分析 总被引:1,自引:0,他引:1
目的探讨中国汉族人中α1抗糜蛋白酶(AACT)基因、早老素1(PS1)基因多态性与阿尔茨海默病(Alzheimersdisease,AD)的相关情况。方法应用PCRRFLP方法,在123例患者和140例正常人中观察AACT信号肽和PS1基因多态性的分布,进行关联分析。结果1AD患者与PS1基因等位基因1正关联,与等位基因2和基因型2/2负关联,但与1/1基因型无关;2AACT信号肽基因多态性与AD无关联;3在三种PS1基因型中,AACT信号肽基因多态性与AD均无关;4在AACT基因AA、TT基因型中,PS1基因多态性与AD负关联,而TA型中PS1基因与AD无显著相关。结论中国人群中,AD与PS1基因2/2型负关联,而与AACT信号肽基因多态性无关;AACT信号肽和PS1基因多态性之间也无明显的相互影响。 相似文献
84.
Piñon M Racotta IS Ortiz-Butron R Racotta R 《Journal of the autonomic nervous system》1999,75(2-3):131-135
Paraganglia are clusters of cells containing catecholamines (CA), mainly norepinephrine (NE) and dopamine (DA). The presence of epinephrine (E), on the other hand, has only been determined by indirect methods in retroperitoneal paraganglia of newborn and aged rats. Because their location, paraganglia associated with the hepatic branch of the vagus nerve may be a possible source of CA for the liver. The main purposes of the present study were to determine CA levels and whether E can be found in the omentum minus which includes paraganglia associated with the hepatic branch of the vagus nerve, and then to study the effects of 6-hydroxydopamine and reserpine on their CA content. Twenty-four female Wistar rats were randomly ascribed to three groups receiving two intraperitoneal injections of either 6-hydroxydopamine, reserpine or saline. Twenty-four hours after the last administration the rats were anesthetized and a portion of the omentum minus was obtained. Left adrenal medulla and a liver fragment were also collected as controls. The samples were processed to be analyzed by high performance liquid chromatography and catecholamine histofluorescence. The results confirm previous reports about the presence of considerable amounts of norepinephrine and dopamine in paraganglia. Norepinephrine and dopamine in the omentum like the adrenal medulla were significantly depleted by reserpine but not by 6-hydroxydopamine treatment, suggesting that some other sources in addition to sympathetic terminals are responsible for CA in the omentum. On the contrary, both drugs reduced liver NE, consistent with the localization of this amine mainly to hepatic sympathetic terminals. Histofluorescence of the omentum revealed 2-4 paraganglia per tissue fragment. Paraganglia associated with the hepatic branch of the vagus nerve contain also E. The presence of perihepatic sources of extra-adrenal CA, and more specifically E, could be of physiological significance. 相似文献
85.
Hammond EH Henson DE;Cancer Committee College of American Pathologists;Task Force on the Examination of Specimens Removed from Patients with Bladder Cancer 《Archives of pathology & laboratory medicine》1996,120(12):1103-1110
This article details a practice protocol for the examination and reporting of specimens removed from patients with carcinoma of the urinary bladder, ureter, renal pelvis, or urethra. It was created by a multidisciplinary task force of pathologists and oncologists established by the Cancer Committee of the College of American Pathologists. Documentation for the protocol was obtained from the previously published protocol, the medical literature, personal experience, and consultation with colleagues. After creation and review by the task force, the protocol was sent to 1000 randomly selected practicing pathologists as a survey. Their comments and suggestions were addressed in the final version. The protocol was approved by the Board of Governors of the College of American Pathologists. 相似文献
86.
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International Workshop on the Impact of the Environment on Reproductive Health 《Progress in human reproduction research》1991,(20):1-11
The WHO workshop on the impact of the environment on reproductive health is summarized. Topics include the nature of environmental factors affecting reproductive health, environmental factors blamed for declining sperm quantity and quality, the effects of natural and man-made disasters on reproductive health, chemical pollutants, how the environment damages reproductive health, and research needs for better research methodologies and surveillance data. Recommendations are made to: 1) promote international research collaboration with an emphasis on consistency of methodological approaches for assessing developmental and reproductive toxicity, on development of improved surveillance systems and data bases, an strengthening international disaster alert and evaluation systems; 2) promote research capabilities for multidisciplinary studies, for interactive studies of the environment and cellular processes, and for expansion of training and education; and 3) take action on priority problems of exposure to chemical, physical, and biological agents, of exposure to pesticides among specific populations, and of inadequate screening methods for identification of environmental chemicals. The costs of environmental injury to reproduction include subfertility, intrauterine growth retardation, spontaneous abortion, and various birth defects. Developed country's primary threats are from chemical pollution, radiation, and stress. There is a large gap in knowledge. Caution is urged in understanding the direct relationship between environmental causes and infertility. Sexual health is difficult to assess and research is suggested. Exposure to excessive vitamin A and toxic chemicals are cited as agents probably having serious effects on malformations. Sperm quality has declined over the decades; there is speculation about the potential causes. The effects of radiation such as at Chernobyl are described. Toxic chemical exposure such as in Bhopal, India killed thousands. Neurological damage is reported for fetuses and infants exposed to methyl mercury. There is the beginning of evidence that complications of pregnancy may be related to pollution levels surrounding industrial plants. Reproductive health is affected through chromosome damage and cell destruction, prenatal death, altered growth, fetal abnormalities, postnatal death, functional learning deficits, and premature aging. 相似文献
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