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91.
Bellintani-Guardia B Ott M 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》2002,145(1):56-63
Retinal ganglion cells were successfully labelled in the chameleon by retrograde axonal transport of dextran amines that were applied to the nucleus of the basal optic root (nBOR) in an in vitro preparation. Labelled ganglion cells were restricted to the contralateral eye. Many cells were completely stained including their dendritic trees. With few exceptions, all cells had displaced somata that were located at the inner margin of the inner nuclear layer. The labelled ganglion cells had two to six primary dendrites that branched frequently and formed large unistratified dendritic trees within sublamina 1 of the inner plexiform layer. There was extensive overlap of the dendritic trees of neighbouring cells leading to an estimated coverage factor of 2-4. The dendritic field areas varied in size according to the retinal position of the cells and were highest in the central retina around the fovea with a maximum of 0.14 mm(2) and reached a second maximum at the retinal margin with values of 0.08-0.1 mm(2). The smallest dendritic areas (0.04-0.06 mm(2)) were measured midway between the fovea and retinal margin. The size of the soma area was not correlated to the dendritic field size and increased from 100 to 150 microm(2) near the fovea to 150-300 microm(2) at the retinal margin. There was no evidence for a retinotopic organisation of ganglion cell fibres within the nBOR. All cells were of uniform morphology that was identical to the type of nBOR-projecting displaced ganglion cell (DGC) described previously for the bird retina. Similar to birds, the labelled DGCs were the only source of retinal projection to the nBOR. A small fraction of cells had orthotopic somata located in the ganglion cell layer but were otherwise identical to the labelled DGCs. The similarity of chameleon nBOR-projecting ganglion cells to those described in avian retinas mirrors the close phylogenetic relationship of birds and lizards. 相似文献
92.
目的研究外周神经损伤后背根神经节细胞中Ephrin B1及其相关受体的表达变化。方法建立一侧坐骨神经夹伤的大鼠动物模型,通过免疫荧光组织化学方法检测受损侧背根神经节细胞中Ephrin B1及其相关受体Eph B1、Eph B2、Eph B3和Eph A4、RYK等的表达,并分析阳性细胞数和不同大小阳性细胞的构成比例。结果外周坐骨神经受损侧背根神经节细胞中Ephrin B1的表达明显减弱,而Eph B1、Eph B2、Eph B3和Eph A4受体的表达无明显变化,但RYK受体的表达则明显加强。结论Ephrin B1和RYK受体在一侧外周坐骨神经夹伤后的大鼠背根神经节细胞中表达的变化,说明它很有可能参与了损伤后的功能活动。 相似文献
93.
Stanley G. Rane George G. Holz IV Kathleen Dunlap 《Pflügers Archiv : European journal of physiology》1987,409(4-5):361-366
Dihydropyridine (DHP) calcium channel antagonists, which inhibit the slowly inactivating or L-type cardiac calcium (Ca) current, have been shown to be ineffective in blocking45Ca influx and Ca-dependent secretion in a number of neuronal preparations. In the studies reported here, however, the antagonist DHP nifedipine inhibited both the L-type Ca current and potassium-evoked substance P (SP) release from embryonic chick dorsal root ganglion (DRG) neurons. These results suggest that, in DRG neurons. Ca entry through L-type channels is critical to the control of secretion. The inhibition of Ca current by nifedipine was both voltage and time-dependent, significant effects being observed only on currents evoked from relatively positive holding potentials maintained for several seconds. As expected from these results, nifedipine failed to inhibit L-type Ca current underlying the brief plateau phase of the action potential generated from the cell's normal resting potential; likewise, no significant effect of the drug was observed on action potential-stimulated SP release evoked by electrical field stimulation. The results of this work are discussed in terms of an assessment of the role of L-type Ca channels in neurosecretion.This work was supported by United States Public Health Service Grant NS16483 (KD) and by a USPHS Postdoctoral Fellowship (SGR) 相似文献
94.
Objective and design: The present study examined effectiveness of low-dose doxycycline (LDD) in combination with nonsurgical therapy on gingival
crevicular fluid (GCF) tissue plasminogen activator (t-PA) levels and clinical parameters in chronic periodontitis (CP) a
over 12-month period.
Methods: GCF samples were collected, probing depth (PD), clinical attachment level (CAL), gingival index (GI) and plaque index were
recorded at baseline, 3, 6, 9 and 12 months. CP patients (n = 65) were randomized to LDD or placebo groups. LDD group received
LDD (20 mg) b.i.d for 3-months plus and root planing (SRP), while placebo group was given placebo capsules b.i.d for 3-months
plus SRP. GCF t-PA levels were determined by ELISA. Friedman, Wilcoxon and Mann-Whitney test was used for statistical analysis.
Results: Significant improvement was observed in all clinical parameters in both groups over 12-month period (p < 0.01). LDD group
had lower PD, CAL and GI scores than placebo group at 6, 9 and 12-months (p < 0.05). GCF t-PA levels reduced in both groups
over 12-month period (p < 0.01). LDD group had lower GCF t-PA levels than placebo group at 6 and 9-months (p < 0.05).
Conclusions: These results provide additional information about usefulness of LDD therapy as an adjunct to nonsurgical therapy in long-term
management of periodontitis.
Received 8 May 2006; returned for revision 13 June 2006; accepted by J. Di Battista 12 July 2006 相似文献
95.
目的:为C7神经移位椎管内吻合腰神经前根重建截瘫患者屈髋伸膝功能提供解剖学基础。方法:在20例成人尸体标本上,观测L1阶段椎管内L1~4神经前根排列及纤维数、C7神经转移路径距离及坐骨神经可切取长度及远端纤维数。结果:一侧C7神经经椎体前通路跨越椎体中线的长度为(2.4±0.58)cm,可与对侧C7神经编织成束。在L1节段,L1~4神经前支可辨认并能编织成束供吻合。胫神经和腓总神经可切取长度(52.35±2.60)cm,(48.20±2.37)cm能够满足C7至L1段椎管的距离(48.35±3.36)cm。一侧胫神经和腓总神经远端纤维数(26856±112),(25700±156)大于一侧腰L1~4神经前支纤维数(20766±354)。结论:坐骨神经可选择为颈7神经移位重建截瘫下肢功能的桥接神经,双侧C7神经可经椎体前通路编织成束作为动力神经源,在L1阶段椎管内吻合L1~4腰神经前根的具有可行性。 相似文献
96.
胸腰脊神经根鞘形态观测及其临床意义 总被引:9,自引:1,他引:9
目的:为了探讨腰腿疼痛等疾病与脊神经根鞘的关系。方法:用巨视解剖和游标卡尺测量法对15具尸体的胸腰脊神经根鞘进行了解剖学观察与测量。结果:①左、右胸腰脊神经根鞘长度和横径基本对称;②T1根鞘长度和横径大于其它胸神经根鞘,接近L2水平,L3~L5根鞘长度和横径大于其它胸腰神经根鞘,尤其L5更为突出;③胸腰脊神经根鞘开口式,由上向下,由2~3孔逐渐减至1孔。结论:①T1、L2~L5脊神经根鞘既长又粗,与周围接触范围大,受损危险增大;②根鞘开口式孔数由上向下减少,发生在鞘内的炎症和肿瘤引起前、后根同时受累的机会增多。 相似文献
97.
Postsynaptic potentials (PSPs) with long latencies were evoked in cat hindlimb motoneurons by stimulation of the distal stump of a cut ventral root. Measurements of their latency and the threshold in the responsible afferent fibers showed that they were produced mainly by the activity of the unmyelinated fibers in the ventral root that enter the spinal cord through the dorsal root. Patterns of PSPs evoked in flexor and extensor motoneurons by ventral root stimulation were similar to those observed in the flexion reflex. 相似文献
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