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31.
In the attempt to gain a broader understanding of the causal relationships behind work-related symptoms of pain in the human
shoulder, monitoring of arm position is crucial. Different methods have been used with varying accuracy. A video-based stereometry
system, using infra-red light and reflecting markers for motion analysis, has been introduced for measurements in the fields
of ergonomics, biomechanics and sports medicine. The purpose of this study is to investigate the sources of error in using
this system for posture registration of the upper limb. Measurements are performed on a calibration fixture, on a mechanical
model of the upper limb and on a subject with an exoskeleton. Particular, attention is given to inconsistencies and relative
errors due to the finite geometrical precision with which the markers are positioned in the calibration fixture and on the
studied objects, the limited capability to align the objects relative to the coordinate system of the calibration fixture
and the errors connected to angular measurements using protractors etc. It is concluded that the system makes a valuable addition
to existing instruments for non-contact posture measurement, and produces position data with an adequate accuracy in normal
handling. 相似文献
32.
目的:探讨雌激素,胎盘生乳素,钙在妊高征发病中的作用及其相互关系,方法:采用放射免疫法及离心分析钙试剂,测定了42例妊高征患者血清雌二醇,胎盘生乳素,钙,磷及尿钙,磷的含量,34例同期门诊正常孕妇作为对照组,结果:轻度妊高征患者血清雌二醇明显增加(P〈0.05)。重度妊高征患者血清胎盘生乳素显著减少(P〈0.05),轻,中,重度妊高征患者血钙,尿钙含量显著降低(P〈0.05,P〈0.01,P〈0. 相似文献
33.
Population toxicokinetics of tetrachloroethylene 总被引:1,自引:0,他引:1
F. Y. Bois A. Gelman J. Jiang D. R. Maszle L. Zeise G. Alexeef 《Archives of toxicology》1996,70(6):347-355
In assessing the distribution and metabolism of toxic compounds in the body, measurements are not always feasible for ethical
or technical reasons. Computer modeling offers a reasonable alternative, but the variability and complexity of biological
systems pose unique challenges in model building and adjustment. Recent tools from population pharmacokinetics, Bayesian statistical
inference, and physiological modeling can be brought together to solve these problems. As an example, we modeled the distribution
and metabolism of tetrachloroethylene (PERC) in humans. We derive statistical distributions for the parameters of a physiological
model of PERC, on the basis of data from Monster et al. (1979). The model adequately fits both prior physiological information
and experimental data. An estimate of the relationship between PERC exposure and fraction metabolized is obtained. Our median
population estimate for the fraction of inhaled tetrachloroethylene that is metabolized, at exposure levels exceeding current
occupational standards, is 1.5% [95% confidence interval (0.52%, 4.1%)]. At levels approaching ambient inhalation exposure
(0.001 ppm), the median estimate of the fraction metabolized is much higher, at 36% [95% confidence interval (15%, 58%)].
This disproportionality should be taken into account when deriving safe exposure limits for tetrachloroethylene and deserves
to be verified by further experiments.
Received: 20 April 1995/Accepted: 24 August 1995 相似文献
34.
Nobutaka Eiraku Shinji Ijichi Shinji Yashiki Mitsuhiro Osame Shunro Sonoda 《Journal of neuroimmunology》1992,37(3):223-228
The in vitro proliferation of peripheral blood lymphocytes (PBLs) without any mitogenic stimulation is one of the hallmarks of human T lymphotropic virus type I (HTLV-I) infection. Recent evidence suggests a difference in the degree of the phenomenon between HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) and asymptomatic HTLV-I carriers (AC). In this article, we demonstrated several alterations in the features of the in vitro transformed lymphocytes between patients with HAM/TSP (n = 16) and AC (n = 8). The percentages of total CD8+ and CD8+CD28+ cells were significantly increased in the in vitro proliferating T lymphocytes derived from the patients with HAM/TSP when compared to those from AC. HAM/TSP was segregated from AC by the high degree of the proliferation of CD8+CD28+ cells. The expression of HTLV-I-specific antigens on the cultured PBLs was detected only in the subjects which showed low CD8+CD28+/CD4+ ratio of the in vitro proliferating lymphocytes. These findings suggest that this phenomenon distinguishes HAM/TSP from AC, not only in quantity but also in quality. 相似文献
35.
图娅 《北京中医药大学学报》1997,(5)
21世纪中医学的发展,面临着理顺民族性表述方式与国际性科学内涵关系的问题,因此必须辩证地把握结构与机能、实证科学手段与人文精神、过程与结果之间的谐调统一,这样既符合中医学术体系特征,又能与当代生命科学研究保持一致。 相似文献
36.
P. Brouqui C. Le Cam P. J. Kelly R. Laurens A. Tounkara S. Sawadogo V lo-Marcel L. Gondao B. Faugere J. Delmont A. Bourgeade Prof. D. Raoult 《European journal of epidemiology》1994,10(6):695-698
Human ehrlichiosis is a recently recognized rickettsial disease. It is caused byEhrlichia chaffeensis, an intraleucocytic Gram-negative, obligate intracellular bacterium, grouped within the genusEhrlichiae. Most human cases of ehrlichiosis have been diagnosed in the USA. Two cases have been reported outside of the USA, one in Europe and one in Africa. From 1 January to 30 June 1992, 765 sera from blood donors or other asymptomatic subjects in 8 African countries, including Ivory Coast, Burkina Faso, Mali, Central African Republic, Angola, Zimbabwe, Mozambique and Commores Islands, were tested by indirect immunofluorescence for the presence ofE. chaffeensis antibodies. Positive sera were confirmed by Western immunoblotting. Only two of 765 sera tested were positive. One serum obtained from Burkina Faso had an IgG titer of 1:200 and one from Mozambique had an IgG titer of 1:80. Human ehrlichiosis seems to occur infrequently in Africa, although many more sera from additional African countries need to be evaluated. 相似文献
37.
Dr. David M. Euhus MD Lucille Kimura PhD Bruce Arnold MD 《Annals of surgical oncology》1997,4(5):432-439
Background: Mice immunized with murine mammary carcinoma cells genetically engineered to secrete interleukin-2 (IL-2) are rendered resistant
to subsequent challenge with unmodified tumor cells, and in the case of mice bearing established tumors, the rate of development
of pulmonary metastases is reduced. Despite these encouraging animal results, little is known about the induction of antitumor
immunity by IL-2 gene transfer in human breast cancer.
Methods: Adenovirally mediated IL-2 gene transfer was performed in 12 tumor fragment cultures established from seven primary breast
cancers. Autologous tumor infiltrating lymphocytes (TILs) or peripheral blood mononuclear cells (PBMCs) were cocultured with
transduced tumor fragments, and changes in phenotype and cytotoxicity were measured.
Results: IL-2 was never detectable in the untransduced cultures, but it peaked at 5.0—1,324.8 ng/ml in the transduced cultures. Lymphocyte
counts declined in all untransduced cultures, but they increased two- to sevenfold in four transduced cultures. CD4:CD8 ratios
decreased from a mean of 2.11 at baseline to 1.27 after stimulation in coculture (p=0.03). Expansion of lymphocytes expressing
the natural killer cell phenotype (CD3−CD56+) occurred in only one culture, but the CD3+CD56+ population increased in four of six cultures. Lymphocytes from four of 10 cocultures generated significant cytotoxicity against
allogeneic breast cancer cells. Induction of cytotoxicity correlated with expansion of the CD3+CD56+ phenotype (R2=0.805, p=0.02).
Conclusions: IL-2 gene expression by human breast cancer causes expansion of CD3+CD56+ cytotoxic lymphocytes. This phenotype is consistent with that of a non-major histocompatibility complex (MHC)-restricted
cytokine induced killer cell population previously described.
Opinions, interpretations, conclusions and recommendations are those of the author and are not necessarily endorsed by the
U.S. Army.
Presented at the 49th Annual Cancer Symposium of The Society of Surgical Oncology, Atlanta, Georgia, March 21–24, 1996. 相似文献
38.
Erythromycin administration has been associated with a prolongation of cardiac repolarization in certain clinical settings.
This could be due to blockade of voltage-dependent K+ channels in the human heart. For this reason we examined the effects of erythromycin on a rapidly activating delayed rectifier
K+ channel (Kv1.5) cloned from human heart and stably expressed in human embryonic kidney cells. When examined using the whole-cell
patch clamp technique, erythromycin (100 μM) blocked Kv1.5 current in a time-dependent manner but required prolonged exposure
to do so. However, when we examined Kv1.5 current using inside-out macropatches, erythromycin applied to the cytoplasmic surface
rapidly (within 1-2 min) inhibited Kv1.5 current with an IC50 value of 2.6 x 10-5M (1.7 - 3.9 x 10-5M, 95% C.L.). The main effect of erythromycin was to accelerate the rate of Kv1.5 current decay thereby reducing the current
at the end of a prolonged voltage-clamp pulse. Erythromycin also blocked Kv1.5 current in both a voltage- and frequency-dependent
manner but had little effect on the activation kinetics, deactivation kinetics, or the steady-state inactivation properties
of Kv1.5. These data suggest that erythromycin acts as a blocker of an activated state of the Kv1.5 channel and that it may
access its binding site from the intracellular face of the channel. This study is the first to examine the effects of erythromycin
on a cloned human cardiac K+ channel. It is concluded that erythromycin blocks Kv1.5 at clinically relevant concentrations. Blockade of voltage-dependent
K+ channels in the heart could contribute to the alterations in cardiac repolarization that have been observed with erythromycin.
Received: 22 November 1996 / Accepted: 26 February 1997 相似文献
39.
M. Kneissel P. Roschger W. Steiner D. Schamall G. Kalchhauser A. Boyde M. Teschler-Nicola 《Calcified tissue international》1997,61(2):95-100
There is abundant data on cancellous bone in the aging human spine, but little relating to the growing vertebral cancellous
bone in childhood and adolescence. The purpose of this study was to map vertebral cancellous bone in a growth and age series
of historic skeletal samples and to make comparisons with data published on recent material. Lumbar vertebral bodies were
collected from 65 skeletons (0–60 years) from a medieval Nubian population. Ethnohistoric information was collected to interpret
conditions that might have influenced bone structure and metabolism. The cancellous bone was studied three dimensionally,
using stereophotography and scanning electron microscopy and morphometrically by performing a semiautomatic structural analysis
on digitized backscattered electron images of polymethacrylate-embedded material. The cancellous bone structure in the children
consisted mainly of a densely packed, uniform network of small rodlike trabeculae. The greatest bone volume fraction with
small, more platelike trabeculae was observed during adolescence. In young adults, larger platelike trabeculae were present
in the central zone and smaller trabeculae in the superior and inferior zones, as described for modern skeletal material.
Structural changes associated with aging were observed much sooner than in modern man. By the estimated age of approximately
50–60 years, the predominant architectural elements were slender rarified rods in both sexes. The ethnohistorical data suggest
that this was essentially a black African population of physically active peasants, not likely to suffer Vitamin D insufficiency
or deficient calcium intake. Thus an earlier onset of the biological age changes in cancellous bone found in modern populations
was probably prevalent.
Received: 1 March 1996 / Accepted: 31 December 1996 相似文献
40.
Intracellular recordings from neurons were carried out in cortical slices obtained from tissue removed from patients suffering from intractable seizures. The patients were divided into two groups based on the presence or absence of an anatomical abnormality that could be imaged preoperatively. The lesion or its surround was the presumptive epileptogenic area. The tissue removed from the patients without lesions was removed either for biopsy purposes or for access to epileptic tissue and was not considered epileptogenic. All neurons from patients without an imageable lesion, and some (19%) from patients with an imageable lesion, responded to orthodromic stimuli with a sequence of synaptic excitation followed by inhibition; these properties resembled those of normal rodent cortical slices. Different responses, classified as abnormal, were observed in 81% of the neurons in tissue specimens obtained near lesions. The most common was prolonged synaptic excitation with no noticeable inhibition, even at high stimulus strengths. In three resections, long latency all-or-none depolarization shifts were observed that resemble the classic paradoxical depolarization shift seen in in vivo extracellular recordings. Loss of specific inhibitory systems within the cortex may contribute in part to these abnormal responses. 相似文献