全文获取类型
收费全文 | 210482篇 |
免费 | 15278篇 |
国内免费 | 749篇 |
专业分类
耳鼻咽喉 | 2295篇 |
儿科学 | 5485篇 |
妇产科学 | 4304篇 |
基础医学 | 27137篇 |
口腔科学 | 4533篇 |
临床医学 | 20063篇 |
内科学 | 44946篇 |
皮肤病学 | 2756篇 |
神经病学 | 20315篇 |
特种医学 | 6952篇 |
外国民族医学 | 13篇 |
外科学 | 32967篇 |
综合类 | 3412篇 |
现状与发展 | 2篇 |
一般理论 | 291篇 |
预防医学 | 19071篇 |
眼科学 | 4373篇 |
药学 | 14393篇 |
1篇 | |
中国医学 | 374篇 |
肿瘤学 | 12826篇 |
出版年
2023年 | 846篇 |
2022年 | 1406篇 |
2021年 | 3440篇 |
2020年 | 2109篇 |
2019年 | 3393篇 |
2018年 | 3973篇 |
2017年 | 3223篇 |
2016年 | 3415篇 |
2015年 | 4069篇 |
2014年 | 6100篇 |
2013年 | 8833篇 |
2012年 | 13128篇 |
2011年 | 14330篇 |
2010年 | 8110篇 |
2009年 | 7313篇 |
2008年 | 13593篇 |
2007年 | 14433篇 |
2006年 | 13927篇 |
2005年 | 14398篇 |
2004年 | 13816篇 |
2003年 | 12906篇 |
2002年 | 12447篇 |
2001年 | 1889篇 |
2000年 | 1471篇 |
1999年 | 2055篇 |
1998年 | 2829篇 |
1997年 | 2440篇 |
1996年 | 2208篇 |
1995年 | 1957篇 |
1994年 | 1762篇 |
1993年 | 1658篇 |
1992年 | 1216篇 |
1991年 | 1154篇 |
1990年 | 1056篇 |
1989年 | 963篇 |
1988年 | 1023篇 |
1987年 | 1024篇 |
1986年 | 999篇 |
1985年 | 1088篇 |
1984年 | 1484篇 |
1983年 | 1466篇 |
1982年 | 1816篇 |
1981年 | 1645篇 |
1980年 | 1556篇 |
1979年 | 816篇 |
1978年 | 958篇 |
1977年 | 932篇 |
1976年 | 831篇 |
1975年 | 682篇 |
1974年 | 667篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Hayato Kihara Arvan L. Fluharty John S. O'Brien Charles H. Fish 《Clinical genetics》1982,21(4):253-261
A patient with neuropathy and myopathy since infancy but whose neuropathy had been stable for a number of years showed a profound deficiency of arylsulfatase A in leukocytes and urine. Urine contained material that stained metachromatically and cochromatographed with cerebroside sulfate. In contrast, cultured fibroblasts contained about 10-20% of normal arylsulfatase A with properties identical to properties of normal fibroblast enzyme, except that it showed no cerebroside sulfatase activity. Growing fibroblasts in the cerebroside sulfate loading test had an attenuated rate of sulfatide hydrolysis. A re-examination of the cerebroside sulfatase reaction revealed that while only limited hydrolysis occurred with low concentrations of taurodeoxycholate or cholate (type I activation), significant hydrolysis of the natural substrate did take place with high concentrations of cholate (type II activation). This suggests that there is a partial cerebroside sulfatase defect in this atypical form of metachromatic leukodystrophy. 相似文献
992.
993.
Mariz Vainzof Mayana Zatz Paulo A. Otto John M. Opitz James F. Reynolds 《American journal of medical genetics. Part A》1985,22(1):81-87
Serum creatine-kinase (CK) isoenzyme MB was measured in 53 patients affected by different types of myopathies (20 with Duchenne muscular dystrophy (DMD), eight with the Becker form (BMD), ten with the limb-girdle form (LGMD), six with the facioscapulohumeral form (FSH), and nine affected by polymyositis and in 21 normal control subjects). The aim of this study was to compare each group with the control individuals and to assess the nosologic value of CK-MB activity among some clinically similar dystrophies, which may have an important application for genetic counseling. A statistically significant increased CK-MB activity was found only in the Duchenne and Becker patients when compared with control persons (p < 0.05). When the different groups of patients were compared among themselves, no significant difference was found between DMD and BMD or LGMD and polymyositis. However, a significant difference was found between BMD and LGMD. Based on these data, it is possible, through discriminant analysis, to estimate the relative biochemical probability of an isolated male patient belonging to either group. 相似文献
994.
This study examines harmaline-induced changes in 5′-nucleotidase (5′-ND) activity in cerebellar fractions from rats with an intact inferior olive (IO) or prior destruction of the IO by 3-acetylpyridine (3-AP) intoxication. Harmaline markedly increased 5′-ND activity in the crude homogenate (P<0.05) and P2 fraction (P<0.001) of cerebella from rats with an intact IO. This increase was absent in the P1, P3 and S3 fractions and it was abolished by 3-AP olivectomy. It was also absent in basal ganglia P2 fractions. Since harmaline produces rhythmic complex spike discharges of Purkinje cells by activating IO neurons [4, 18], these data suggest that climbing fiber activation per se increases 5′-ND activity in the P2 fraction. This raises the possibility that a climbing fiber-induced local increase in 5′-ND activity at parallel fiber-Purkinje cell synapses results in a local increase in adenosine concentration. This may account for climbing fiber-evoked suppression of simple spike activity [12, 13, 28]. 相似文献
995.
John Scott Frazer Amelia Shard James Herdman 《Journal of medical engineering & technology》2020,44(4):169-176
AbstractThe ongoing COVID-19 pandemic is unprecedented in the modern age both due to its scale and its disruption to daily life throughout the world. Widespread social isolation and restrictions in the age of modern communicative technology, coupled with some early successes for makers, have united the open-source community towards a common goal in a way not previously seen. Local hospitals and care facilities are turning to makers to print essential consumable parts, such as simple visors, while in the hardest hit areas, critical pieces of medical technology are being fabricated. While important and effective innovations are appearing almost daily, there are also some worrying trends towards hobbyists attempting manufacture of complex medical devices with little understanding of the clinical or scientific rationale behind their design. The nature of the open-source community, an area of intensive innovation, fluidity, and experimentation, jars with the exacting standards of medical device regulation. Here, we review the involvement of rapid prototyping and the open-source community in the key areas of personal protective equipment (PPE), diagnostics, critical care technology, and information acquisition and sharing, highlighting where makers and hackers have clashed with medical device regulations, and areas where the system has worked well to facilitate change. 相似文献
996.
Gerhard Neuhser Richard F. Daly Norma C. Magnelli Robert F. Barreras Robert M. Donaldson John M. Opitz 《Clinical genetics》1976,9(1):81-91
The familial occurrence of essential tremor combined with (congenital) nystagmus, duodenal ulceration and a narcolepsy-like sleep disturbance caused by an autosomal dominant gene with high penetrance and fairly uniform expressivity is reported in a family of Swedish-Finnish ancestry. Twelve of 17 affected family members had essential tremor which began between 30-40 years of age and which could be controlled temporarily by alcohol; this resulted in alcoholism in several affected individuals. The most severly affected persons showed cerebellar signs which may reflect a possible pathogenetic relationship of the syndrome to the genetic cerebellar atrophies. Nystagmus, observed in 12 of 17 affected family members (eight of whom were also affected with tremor) usually was congenital and accompanied by refractive errors. Duodenal ulcers occurred almost exclusively in individuals with the neurological syndrome, and preceded its onset in some cases. The ulcer disease therefore seems to be a component manifestation of the syndrome and is interpreted as a pleiotropic effect of the gene which also causes the nystagmus, tremor and sleep disturbance. 相似文献
997.
Brian T. Butcher Carol E. ONeil Margaret A. Reed John E. Salvaggio Hans Weill 《The Journal of allergy and clinical immunology》1982,70(4):231-235
Toluene diisocyanate (TDI) sensitivity accompanied by nonspecific bronchial hyperresponsiveness occurs in approximately 5% of occupationally exposed workers. We report the case of a 32-yr-old worker followed longitudinally after removal from isocyanate exposure. TDI reactivity was lost 11 mo after removal from exposure and nonspecific bronchial hyperresponsiveness resolved after 17 mo. Bronchial reactivity to radishes (Raphanus sativus), which developed concurrently with TDI reactivity, was lost 2 yr later. Immunopharmacologic results show that the worker's initial decreased ability of lymphocytes to produce cyclic AMP returned to near normal after 2 yr. IgE antibodies to a human serum albumin tolyl monoisocyanate conjugate were still present at this time. 相似文献
998.
Steroid hormones regulate sexual behavior primarily by slow, genomically mediated effects. These effects are realized, in part, by enhancing the processing of relevant sensory stimuli, altering the synthesis, release, and/or receptors for neurotransmitters in integrative areas, and increasing the responsiveness of appropriate motor outputs. Dopamine has facilitative effects on sexual motivation, copulatory proficiency, and genital reflexes. Dopamine in the nigrostriatal tract influences motor activity; in the mesolimbic tract it activates numerous motivated behaviors, including copulation; in the medial preoptic area (MPOA) it controls genital reflexes, copulatory patterns, and specifically sexual motivation. Testosterone increases nitric oxide synthase in the MPOA; nitric oxide increases basal and female-stimulated dopamine release, which in turn facilitates copulation and genital reflexes. Serotonin (5-HT) is primarily inhibitory, although stimulation of 5-HT(2C) receptors increases erections and inhibits ejaculation, whereas stimulation of 5-HT(1A) receptors has the opposite effects: facilitation of ejaculation and, in some circumstances, inhibition of erection. 5-HT is released in the anterior lateral hypothalamus at the time of ejaculation. Microinjections of selective serotonin reuptake inhibitors there delay the onset of copulation and delay ejaculation after copulation begins. One means for this inhibition is a decrease in dopamine release in the mesolimbic tract. 相似文献
999.
α-Amino-iso-butyrate (AIB) inhibits long-term, protein synthesis-dependent memory formation by reducing labelled leucine uptake in vivo without affecting leucine incorporation into protein. Unlike the antibiotic cycloheximide, AIB does not block long-term memory formation through inhibition of protein synthesis per se. The behavioural effect of AIB is restricted to times of administration between 5 min before and 5 min after learning a single trial passive avoidance task by day-old chickens. It is concluded that (1) AIB competes with normal amino acids for uptake into cells, and (2) the uptake of amino acids for protein synthesis specific to long-term memory formation takes place in the first few minutes following learning. 相似文献
1000.