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排序方式: 共有2419条查询结果,搜索用时 15 毫秒
91.
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93.
Physical activity and ethnic differences in hypertension prevalence in the United States 总被引:3,自引:0,他引:3
BACKGROUND: In the United States, non-Hispanic blacks have higher rates of hypertension than other ethnic groups. In addition, they have higher rates of physical inactivity, a behavior linked to high blood pressure. We examined associations between ethnicity, leisure-time physical activity (LTPA), and hypertension prevalence in a representative sample of U.S. adults. METHODS: Using data on 16,246 adults in the third National Health and Nutrition Examination Survey, hypertension prevalence was determined for non-Hispanic white, non-Hispanic black, and Mexican Americans at various levels of LTPA (none, 0.1-4.9 bouts/week at any intensity, 5+ bouts/week of moderate-to-vigorous activity). Logistic regression was used to examine relationships between hypertension prevalence, race, LTPA, and other variables. RESULTS: Hypertension prevalence was significantly less in the most active group, compared with their sedentary peers (odds ratio = 0.73, CI 0.59 to 0.90). Blacks had an odds ratio for hypertension of 1.77 (CI 1.49 to 2.10) compared with non-Hispanic whites, after adjusting for gender, age, income, LTPA, smoking, BMI, salt intake, rural/urban dwelling, and alcohol intake. Mexican Americans had an adjusted odds ratio of 0.75 (CI 0.62 to 0.89), relative to non-Hispanic whites. CONCLUSION: Ethnicity and LTPA are both associated with hypertension prevalence after controlling for each other, as well as other confounders. Thus, race and physical activity are important independent contributors to hypertension prevalence. 相似文献
94.
There is consistent evidence that the principal etiology of schizophrenia involves predisposing genetic factors. Recent years
have seen several new insights in the genetics of schizophrenia. Several chromosomal regions show significant evidence that
they contain schizophrenia susceptibility genes. A clinically relevant genetic subtype of schizophrenia (22q deletion syndrome)
has been identified. There is new evidence that spontaneous mutations may play a role. There are new recommendations for genetic
counseling. The progress to date suggests that understanding of a neurodevelopmental pathway from genetic susceptibility to
schizophrenia will soon be fundamentally altered by molecular genetic advances in this complex disease. 相似文献
95.
Limiting factors for maximum oxygen uptake and determinants of endurance performance 总被引:30,自引:0,他引:30
In the exercising human, maximal oxygen uptake (VO2max) is limited by the ability of the cardiorespiratory system to deliver oxygen to the exercising muscles. This is shown by three major lines of evidence: 1) when oxygen delivery is altered (by blood doping, hypoxia, or beta-blockade), VO2max changes accordingly; 2) the increase in VO2max with training results primarily from an increase in maximal cardiac output (not an increase in the a-v O2 difference); and 3) when a small muscle mass is overperfused during exercise, it has an extremely high capacity for consuming oxygen. Thus, O2 delivery, not skeletal muscle O2 extraction, is viewed as the primary limiting factor for VO2max in exercising humans. Metabolic adaptations in skeletal muscle are, however, critical for improving submaximal endurance performance. Endurance training causes an increase in mitochondrial enzyme activities, which improves performance by enhancing fat oxidation and decreasing lactic acid accumulation at a given VO2. VO2max is an important variable that sets the upper limit for endurance performance (an athlete cannot operate above 100% VO2max, for extended periods). Running economy and fractional utilization of VO2max also affect endurance performance. The speed at lactate threshold (LT) integrates all three of these variables and is the best physiological predictor of distance running performance. 相似文献
96.
Changes in event-related potentials in a three-stimulus auditory oddball task after mild head injury 总被引:4,自引:0,他引:4
Previous research has demonstrated changes in event-related potentials in a variety of cognitive tasks after severe closed head injury. We sought to establish if similar changes were present in patients who had sustained only apparently mild head injury (MHI) by recording event-related potentials in a group of 24 mild head injured and 24 control participants during a three-stimulus auditory target detection task. For this ‘oddball’ task participants were required to press a button every time they heard a rare target tone and to ignore rare novel sounds and frequent non-target tones. Neuropsychological test results indicated that the mild head injured group had mild memory and attention impairments. Analysis of behavioural performance on the three-stimulus ‘oddball’ task showed no difference in reaction times or error rates between the two groups. Target condition N2 deflections appeared to be larger in the mild head injured but peak amplitude measures revealed that this effect was not significant. There were no significant differences in the amplitude or latency of the P3b evoked by target stimuli or the P3a evoked by novel stimuli. However, a putative ‘O-wave’ or ‘reorienting negativity’ following the P3a was more negative in the mild head injured group suggesting increased activation of components of the attention network. These findings lend support to the hypothesis that MHI can cause subtle cognitive impairments that are associated with abnormal allocation of attention resources in the context of normal behavioural performance. 相似文献
97.
Evidence for endogenous formation of tobacco-specific nitrosamines in rats treated with tobacco alkaloids and sodium nitrite 总被引:2,自引:0,他引:2
Carcinogenic tobacco-specific nitrosamines are present in tobacco products
and are believed to play a significant role in human cancers associated
with tobacco use. Additional amounts of tobacco-specific nitrosamines could
be formed endogenously. We tested this hypothesis by treating rats with
nicotine and sodium nitrite and analyzing their urine. Initially, we
treated groups of rats with (S)-nicotine (60 micromol/kg) and NaNO2 (180
micromol/kg), (S)-nicotine alone, NaNO2 alone or
4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK, 12 nmol/kg) by gavage
twice daily for 4 days. We collected urine and analyzed for two metabolites
of NNK; 4-(methylnitrosamino)-1-(3- pyridyl)-1-butanol and its glucuronide.
We did not detect these metabolites in the urine of rats treated with
nicotine alone or nicotine plus NaNO2, indicating that endogenous
conversion of nicotine to NNK did not occur. However, the urine did contain
N'- nitrosonornicotine (NNN), N'-nitrosoanabasine (NAB) and N'-
nitrosoanatabine (NAT). Analysis of the (S)-nicotine used in this
experiment demonstrated that it contained trace amounts of nornicotine,
anabasine and anatabine. In a second experiment, we used an identical
protocol to compare the endogenous nitrosation of this (S)-nicotine with
that of synthetic (R,S)-nicotine, which did not contain detectable amounts
of nornicotine, anabasine or anatabine. NNN (0.53 x 10(-3)% of nicotine
dose), NAB (0.68%) and NAT (2.1%) were detected in the urine of the rats
treated with the (S)-nicotine and NaNO2. NNN (0.47 x 10(- 3)% of dose), but
not NAB or NAT, was present in the urine of the rats treated with synthetic
(R,S)-nicotine and NaNO2. NNN probably formed via nitrosation of
metabolically formed nornicotine. These results demonstrate for the first
time that endogenous formation of tobacco- specific nitrosamines occurs in
rats treated with tobacco alkaloids and NaNO2. The potential significance
of the results with respect to nitrosamine formation in people who use
tobacco products or nicotine replacement therapy is discussed.
相似文献
98.
Expression of differential nitric oxide synthase isoforms in human normal gastric mucosa and gastric cancer tissue 总被引:10,自引:2,他引:10
The present study investigated the expression and distribution of three
isoforms of nitric oxide synthase (NOS) in different anatomical regions of
the human stomach and in gastric neoplastic tissues by immunohistochemistry
using specific antibodies. Intracellular localization of individual
isoenzymes of NOS was detected in normal gastric mucosa. Gastric cancer
tissues had a marked reduction of all three NOS isoforms expression. The
expression of the endothelial NOS, neuronal NOS and inducible NOS in the
tumor tissue was significantly lower than in normal gastric mucosa (P =
0.01, P = 0.02, P < 0.01, respectively). In the tumor tissue the
expression of inducible NOS was significantly lower than the expression of
both constitutive forms of NOS (P < 0.01). There was a tendency to
higher expression of both constitutive forms of NOS in earlier stages T2 of
the tumor compared to advanced T4 tumor. In contrast, the expression of
inducible NOS was higher than in the advanced T4 tumor than in the earlier
stages T2 of the tumor. The mapping of the expression of endothelial NOS,
neuronal NOS and inducible NOS in human stomach showed higher expression of
NOS isoforms in the distal third than in the proximal third of the stomach
(P = 0.03, P = 0.04, P = 0.01, respectively). We conclude that there is
greater expression of NOS in the stomach corpus and in antrum than in the
proximal third of the normal human stomach mirroring the anatomical
predilection of common pathological changes in this part of the human
stomach. Furthermore, there was loss of the expression of individual
isoenzymes in gastric neoplasms.
相似文献
99.
4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) is an important
metabolite of the tobacco-specific nitrosamine 4-(methylnitrosamino)-1-
(3-pyridyl)-1-butanone (NNK). Using the chiral derivatizing agent, (R)-
(+)-alpha-methylbenzyl isocyanate [(R)-(+)-MBIC], previous work has shown
that the enantiomeric ratio of metabolically formed NNAL and its
glucuronide derivative may be species dependent. However, the absolute
configuration of such NNAL has not been previously reported. Synthetically
prepared racemic NNAL was converted to diastereomeric esters by reaction
with (R)-(+)- and (S)-(-)-alpha-methoxy-alpha-
(trifluoromethyl)phenylacetic acid (MTPA) chloride (Mosher's reagent) and
the products were characterized by 1H-NMR. Based on chemical shift data,
the absolute configuration of NNAL in each diastereomeric ester was
assigned. Hydrolysis of (R)-NNAL-(R)-MTPA gave (R)-NNAL. This was converted
to the corresponding carbamate by reaction with (R)-(+)-alpha- MBIC and the
absolute configurations of the diastereomeric carbamates formed by reaction
of (R)- and (S)-NNAL with (R)-(+)-MBIC were thereby assigned. Conversion of
metabolically produced NNAL to the same carbamates allowed us to assign the
NNAL formed from NNK by rat liver microsomes as (R)-NNAL. The major and
minor NNAL-glucuronide diastereomers found in the urine of patas monkeys
and humans exposed to NNK were similarly assigned; they were formed from
(R)-NNAL and (S)- NNAL, respectively.
相似文献
100.