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41.
目的:为了深讨心肌细胞内钙离子浓度的变化与心力衰竭发生的关系。方法:原子吸收分光技术测定红细胞内外Ca2+含量。我们对住院的56例心力衰竭患儿进行了红细胞内及血浆钙离子浓度的测定,并与30例正常小儿对照。结果:心衰患儿红细胞内Ca2+浓度明显升高,血浆Ca2+浓度降低,与对照组相比有非常显著性差异(P<0.001)。其升高程度与心衰呈正相关(r=0.63,P<0.01),即心衰越重,心功能越差,红细胞内Ca2+浓度升高亦越明显。而当心衰纠正,心功能恢复后,红细胞内Ca2+浓度则明显下降,血浆Ca2+浓度也恢复正常。而不同病因所致的心衰,其间红细胞内Ca2+浓度升高程度无明显差异。结论:提示钙离子参与了心力衰竭的发生与发展。 相似文献
42.
用同位素标记~(15)Ca法测定大鼠突触体内游离钙的浓度,探讨了腺苷对高钾、N-甲基-D-天冬氨酸(NMDA)谷氨酸(Glu)等刺激所致的Ca~(2 )内流增加的影响。结果发现腺苷在10nmol/L~0.1μmol/L范围内对高钾、NMDA、Glu等刺激所致的Ca~(2 )内流有抑制作用,并呈剂量依赖关系,最大抑制率分别为41.68±7.68%、31.32±6.17%、37.52±2.29%。这可能是腺苷对缺血性脑损伤保护作用的机理。 相似文献
43.
微量元素锌在佝偻病治疗中的效果观察 总被引:7,自引:1,他引:6
目的 :探讨补充锌 +维生素D +钙剂治疗佝偻病的效果。方法 :随机分为 3组 ,每组各 5 3例。对照组给予常规治疗 (即维生素D +钙剂 ) ,治疗 1组先给予锌治疗 1个月后 +常规治疗 ,治疗 2组同时给予锌 +常规治疗。 3个月为 1疗程。治疗前后检测血清微量元素及骨碱性磷酸酶 (BALP)等项目。结果 :治疗 1、2组疗效好于对照组 ,差异非常显著 (P <0 0 1) ;治疗1组疗效好于治疗 2组 ,差异有显著性 (P <0 0 5 )。结论 :治疗大多数伴低锌的佝偻病先补锌 1个月 ,再加常规治疗 ,疗效更佳。 相似文献
44.
Summary The present report compares the effects of different membrane phospholipid (PL)-cholesterol compositions on the kinetics of liposome-mediated formation of calcium phosphates from metastable solutions (2.25 mM CaCl2; 1.5 mM KH2PO4) at 22°C, pH 7.4 and 240 mOsm. In most experiments, the liposomes were composed of 7:2:X mixtures of phosphatidylcholine (PC), neutral or acidic phospholipids, and cholesterol (Chol, X=0, 10, 35, or 50 mol%). The neutral phospholipids (NPL) examined, in addition to PC, were phosphatidylethanolamine (PE) and sphingomyelin (Sph), and the acidic phospholipids (APL) examined were dicetylphosphate (DCP), dioleolylphosphatidylglycerol (DOPG), dioleolylphosphatidic acid (DOPA), phosphatidylserine (PS) and phosphatidylinositol (PI). The 7:2:X liposomes did not initiate mineralization in metastable external solutions per se or, with the exception of DOPA, show extensive Ca-PL binding. However, solution Ca2+ losses due to precipitation occurred when the liposomes were encapsulated with 50 mM KH2PO4 and made permeable to external Ca2+ with X-537A. The extent of these Ca2+ losses was sensitive to both the phospholipid and Chol makeup of the membrane. Moderate-to-extensive intraliposomal precipitation occurred in all 7PC:2APL and 7PC:2NPL liposomes containing 0 or 10 mol% Chol. In contrast, at 50 mol% Chol, mineralization inside all liposomes was negligible. The only significant discriminating effect on internal mineralization among the different phospholipids was observed at 35 mol% Chol, where mineral accumulations ranged from negligible to moderate. At 0 or 10 mol% Chol, extraliposomal precipitation was extensive in all but DOPA- and PS-containing liposomes. However, onece intraliposomal yields declined at the higher Chol levels, external mineralization was either delayed or totally blocked in all liposome preparations. Other experiments showed that Sph substituted for PC in 7NPL:2DCP:1Chol liposomes totally blocked both intra- and extraliposomal precipitaiton. PE substituted in this manner, however, blocked only extraliposomal precipitation. The results of this study suggest that interference of the membrane transport processes controlling intraliposomal precipitation [15] by high (50 mol%) Chol levels is not significantly compromised by the specific APL or NPL incorporated in the membrane. Similarly, the data suggest that Chol does not directly affect the specfic interactions of the different membrane APLs with the mineral phase. On the other hand, the substitution of other NPLs for PC can affect the role of APLs such as DCP in liposome-mediated mineralization. 相似文献
45.
家兔未成熟心肌缺血再灌注肌浆网摄钙功能的初步研究 总被引:5,自引:2,他引:3
目的 :从亚细胞水平研究未成熟心肌缺血 -再灌注损伤中肌浆网 (SarcoplasmicReticulum ,SR)摄钙功能。方法 :36只家兔随机分为 4组 ,进行离体心灌注。组Ⅰ :幼兔 ,单纯灌注 30min ;组Ⅱ :幼兔 ,停搏 6 0min ,再灌注 30min。组Ⅲ、组Ⅳ为成兔 ,处理分别同组Ⅰ、组Ⅱ ,进行对照。测定各组心功能、冠状动脉流出液血气 ,单细胞内游离钙离子浓度 ([Ca2 + ]i) ,肌浆网Ca2 + -ATPase活性 ,肌浆网45Ca2 + 摄取。结果 :缺血 -再灌注后 ,成熟与未成熟心肌均发生钙超载 (P >0 .0 5 )。未成熟心肌肌浆网Ca2 + ATPase活性 ,肌浆网45Ca2 + 摄取恢复率 ,明显高于成熟心肌 (P <0 .0 5 )。结论 :未成熟心肌缺血 -再灌注损伤钙超载机制不同于成熟心肌 ,肌浆网钙摄取功能 ,在钙超载损伤中不起主要作用。 相似文献
46.
H. B. Jones C. R. Jenkins A. L. Bowdler M. G. Simpson E. A. Lock 《Acta neuropathologica》1997,93(3):241-251
The objectives of the studies described were to assess the ultrastructural neuropathology, blood-brain barrier (BBB) integrity
and calcium status of the cerebellum of rats following a single dose of 750 mg · kg–1
l-2-chloropropionic acid (l-2-CPA). The first indications of intoxication appeared at 36 h when condensation of many granule cells associated with Purkinje
cell degeneration and marked astroglial swelling were observed. Some electron-lucent granule cells were also noted lying amongst
these condensed forms. Condensed granule cells had swollen, electron-lucent mitochondria, dilated Golgi apparatus and nuclear
crenation. Occasionally, areas of granule cell necrosis were also present at this time. Granule cell condensation probably
represents a preliminary and irreversible stage in an excitotoxic process that leads to necrosis. At 48 and 72 h, most granule
cells were necrotic, and occasionally, extravasation of both erythrocytes and leucocytes into the expanded extravascular space
was observed. Evaluation of the BBB by ultrastructural cytochemical visualisation of horseradish peroxidase injected i.v.
2 min before killing by perfusion fixation showed substantial leakage. At 36 h post-dose, ultrastructural calcium localisation
using oxalate/pyroantimonate precipitation demonstrated a substantial increase in calcium pyroantimonate precipitate in mitochondria
and other membranous cytoplasmic organelles (especially the Golgi apparatus) in condensed granule cells, but with little in
their nuclei. However, their immediate neighbours (of ostensibly normal ultrastructural appearances) contained greater amounts
of intranuclear precipitate. Swollen astroglial cells (especially the Bergmann glia) contained considerable quantities of
precipitate. A possible excitotoxic mechanism via l-2-CPA-induced NMDA receptor agonism leading to overwhelming calcium influx and disruption of cellular calcium homeostasis
is proposed.
Received: 8 May 1996 / Revised: 1 September 1996 / Accepted: 11 September 1996 相似文献
47.
Calcium antagonists (CA) exert an anti-atherosclerotic effect in cholesterol-fed rabbits through reduction of cholesterol accumulation in the arterial wall. Further studies in our Institute indicate that verapamil-like compounds and diltiazem stimulate receptor-mediated LDL uptake by human fibroblasts in culture, while nifedipine-like compounds and flunarizine are inactive. Verapamil and diltiazem stimulated LDL-receptor activity also in cells from a heterozygous FH patient, while they were inactive in a receptor defective homozygous FH patient. A basic group needs to be present on the CA molecule to modulate the LDL receptor expression. Preliminary data in our laboratory suggest that some CA can achieve concentrations in the aortic wall likely to exert effects on LDL receptors. This stimulatory activity may improve lipid metabolism in the arterial wall.Corresponding author 相似文献
48.
Andrew P. Thomas Dennis J. Rozanski Dominique C. Renard Emanuel Rubin 《Alcoholism, clinical and experimental research》1994,18(1):121-131
Chronic ethanol consumption leads to a number of alterations in the contractile function of the heart and is a leading cause of cardiomyopathy. Ethanol also has an acute negative inotropic effect mediated by direct interaction with cardiac muscle cells, although this action is often masked by indirect actions resulting from enhanced release of catecholamines in vivo. This article reviews the effects of ethanol on the contractile function of the heart. The specific targets affected by ethanol in cardiac muscle cells are discussed in terms of potential mechanisms underlying the depressions of contractility resulting from both acute and chronic actions of ethanol. 相似文献
49.
磷酸钙骨水泥修复良性骨肿瘤骨缺损 总被引:1,自引:0,他引:1
目的:研究磷酸钙骨水泥(CPC)修复良性骨肿瘤刮除术后遗留的骨缺损的临床应用。方法:应用CPC修复33例患者良性骨肿瘤刮除术后遗留的骨缺损。患者平均年龄38岁,肿瘤类型依次为骨纤维结构不良、骨巨细胞瘤、骨囊肿、动脉瘤样骨囊肿、软骨粘液样纤维瘤、非骨化性纤维瘤、骨母细胞瘤,观察患者术中CPC固化时间,术后全身及切口局部反应,血钙、磷值变化,X线片和CT扫描,平均随访时间19个月。结果:全部患者未见明显不良反应,血钙、磷值未见升高,X线片显示骨缺损处均填充良好,随访见所有患者均有CPC降解和骨替代现象发生。结论:良性骨肿瘤刮除后利用CPC填充修复骨缺损,可充分填充骨肿瘤刮除后不规则瘤腔,即刻恢复骨的强度.经骨替代后可真正完成骨修复。术式简单.并发症少。 相似文献
50.
E. García-Ojeda J.R. Alonso R. Arvalo J.G. Brin J. Lara J. Aijon 《Brain research bulletin》1992,29(6):783-793
The distributions of calbindin D-28K (CaBP) and parvalbumin (PV) in the rat nucleus olfactorius anterior (NOA) were described using monoclonal antibodies and the avidin-biotin-peroxidase method. The NOA showed a high immunoreactivity for CaBP, with a rostrocaudal increase in the positive neurons and fibres. Pars externa (NOAe) was the only subdivision which showed a low CaBP immunostaining. PV-positive elements were less abundant than those CaBP immunostained. The main difference in the distributions for both proteins was observed in the pars medialis which was practically PV negative. PV- and CaBP-stained neurons showed similar morphologies in the subdivisions where they were present. In NOAe, we observed a characteristic PV- and CaBP-positive neuronal type, with an oriented dendritic pattern. Transition areas were clearly observable in both CaBP- and PV-labelled sections. 相似文献