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81.
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83.
Rules to clarify MMPI profiles into four types (P-A-I-N) observed commonly in chronic pain patient populations were tested to determine if resulting average profiles matched computer-algorithm derived prototypes. Close matches were obtained, suggesting that the rules could be used in the ordinary pain clinic setting to look for type x treatment interactions. Seven clinical variables differentiated the types. Type P and N were most different from one another, and Types A and I represented poles on an optimism-pessimism dimension.  相似文献   
84.
This study examined the influence of lateral target motion on the stereothresholds for bright vertical lines at a range of velocities. Stimuli were presented for 200 ms with horizontal velocities from 0 to 12 deg/s. Observers' horizontal eye movements were recorded on additional trials, and confirmed that the velocity of retinal image motion closely matched the velocity of the stimulus. In three auxiliary experiments, stereothresholds were measured (1) after equating the detectability of targets that moved at different velocities, (2) for moving and stationary stimuli with durations between 20 and 200 ms, and (3) for stationary stimuli presented at eccentricities of 0.6 and 1.2 deg. The results indicate that stereothresholds are unaffected by velocities up to approximately 2 deg/s, but worsen in proportion to the velocity at higher speeds. The results of our auxiliary experiments demonstrate that the increase in stereothresholds during image motion cannot be attributed primarily to a reduction in the detectability of the stimulus, a decrease in the effective exposure duration, or non-foveal viewing. We conclude that the elevation of stereo thresholds during lateral motion is consistent with a shift in the sensitivity of the visual system toward lower spatial frequencies as a result of motion blur.  相似文献   
85.
Outcome of corneal transplant rejection: a 10-year study   总被引:2,自引:0,他引:2  
PURPOSE: To study the incidence of graft rejection and the predictive factors for its reversibility. METHODS: It is a retrospective study of 1927 consecutive penetrating keratoplasties performed between January 1990 and January 2000 with more than 6 months follow up. A total of 224 rejection episodes were noted in 183 patients. Of these, 184 first rejection episodes were included in this study. RESULTS: The incidence of first rejection episode was 9.55%. Of patients 87% were symptomatic during the episode with vision loss being the commonest. The average time of onset of rejection was 15.25 +/- 14.4 months (median 11.7 months). In total, 53.3% of rejections occurred within 1 year after surgery. Of the patients who completed minimum 3 months follow up after the rejection episode, the rate of reversibility was 63.3%. Major predictive factors for a poor outcome after rejection were repeated grafting and associated anterior vitrectomy during surgery. The reversibility of the episode did not differ significantly with the modality of treatment used, but treatment with intravenous steroids within 7 days of onset of rejection may have a role in reducing the recurrences of rejection episodes, thus increasing the graft survival. CONCLUSION: Regrafts and associated anterior vitrectomy were significant risk factors for a poor outcome following rejection episode.  相似文献   
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Idiopathic Infantile Arterial Calcification (IIAC) is a rare syndrome of unknown cause characterized by disruption and calcification of the internal elastic laminae of fetal arteries with calcium deposits leading to fibrosis and occlusion of the arteries. The diagnosis is often made at post-mortem examination. However, in a few cases it has been detected prenatally as in this case. Fewer than 10 cases of antenatal detection of this condition have been reported in the literature. In our case, thrombotic microangiopathy was an added feature, which has not been reported thus far in the literature to the best of our knowledge.  相似文献   
88.
This study identified variables which influence the outcome of surgical management on 126 ununited scaphoid fractures managed by internal fixation and non-vascular bone grafting. The site of fracture was defined by a new method: the ratio of the length of the proximal fragment to the sum of the lengths of both fragments, calculated using specific views in the plain radiographs. Bone healing occurred in 71% (89) of cases. Only the site of nonunion (p = 1 x 10(-6)) and the delay to surgery (p = 0.001) remained significant on multivariate analysis. The effect of surgical delay on the probability of union increased as the fracture site moved proximally. A prediction model was produced by stepwise logistic regression analysis, enabling the surgeon to predict the success of surgery where the site of the nonunion and delay to surgery is known.  相似文献   
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Vibrio cholerae O1 El Tor variant strains produced much more cholera toxin than did prototype El Tor strains. The amount of cholera toxin produced by El Tor variant strains both in vitro and in vivo was more or less equivalent to that produced by classical strains.Vibrio cholerae O1 is classified into classical and El Tor biotypes. Among other genetic, biochemical, and physiological differences, each biotype has unique gene sequences encoding cholera toxin B subunit (CTB), that is, classical ctxB and El Tor ctxB. Besides these two prototype biotypes of V. cholerae O1, Nair et al. (9) in 2002 in Bangladesh isolated strains that possess phenotypic properties of both classical and El Tor biotypes carrying classical ctxB. The same group also isolated El Tor strains that had classical ctxB (10). For these new types of strains of V. cholerae O1, we have recently proposed the designations of hybrid and El Tor variants, respectively (13). Subsequent to the isolation of the El Tor variant in Bangladesh by Nair et al. (10), El Tor variant strains were isolated from several countries and areas in Asia and Africa (1, 11, 15-18). In Kolkata, India, we showed that El Tor variant strains appeared in 1990 and that a complete replacement of prototype El Tor strains by El Tor variant strains has occurred since 1995 (14).In this study, we investigated the amount of cholera toxin (CT) produced both in vitro and in vivo by V. cholerae O1 El Tor variant strains isolated in Kolkata during a period from 1996 to 2007. It was found that El Tor variant strains produced a much larger amount of CT than did prototype El Tor strains and that the amount of CT produced by El Tor variant strains was more or less equivalent to that produced by classical strains.V. cholerae O1 strains used in this study are listed in Table Table1.1. AKI (3) and Syncase medium (2) were used for culturing the test strains. The rationale for selecting these media was that AKI preferentially supports the production of El Tor CT (3) while Syncase medium is reported to be the best medium supporting the production of CT by the classical biotype (2). Measurement of CT concentration produced by V. cholerae O1 strains was carried out as follows. Each strain was cultured either in AKI medium at 37°C for 20 h without shaking or in Syncase medium at 37°C for 20 h with shaking, and the optical density of the culture was measured at 600 nm (OD600). After centrifugation, the supernatants were collected and the concentration of CT (ng/ml/OD600) in the samples was measured by bead enzyme-linked immunosorbent assay (ELISA). The method of the bead ELISA employed was essentially that described by Oku et al. (12). In brief, a polystyrene bead (6.5 mm in diameter) was coated with anti-CT IgG and used as a solid phase. The coated bead was first incubated with the sample and then incubated with anti-CT IgG [F(ab′)]-horseradish peroxidase conjugate. Peroxidase activity was determined colorimetrically with 3,3′,5,5′-tetramethylbenzidine as the substrate. The absorbance at 450 nm (OD450) was linear between 0 and 0.5, representing CT concentrations of 0 to 20 ng/ml. The sample prepared as described above (the supernatant of the culture of the strain) was appropriately diluted so that the OD450 fell in the range of 0.1 to 0.5, and the amount of CT produced by the strain was expressed as ng/ml/OD600.

TABLE 1.

V. cholerae O1 strains used
Biotype and straina
El Tor variant
    AM157 (1996), 06-049 (2006), IDH60 (2007), BD200 (2002), 06-098 (2006), CRC220 (2000), AM168 (1996), DO2669 (1998), NLC96 (1999), CRC17 (2000), AM352 (1997), NLC41 (1999), NLC49 (1999), D26942 (1998), SC32 (2003), G27875 (2001), IDH32 (2007), SC216 (2003), NLC8 (1999)
El Tor
    N16961, V100, V114, V113, VC60, M14716, V7, VC64, V54, V24, V32
Classical
    L362, GP15, GP8, GP148, GP147, 569B, GP145
Open in a separate windowaStrains used are listed in the order of CT production (from high to low). The year of isolation is in parentheses.The rabbit ileal loop test was carried out essentially as described by Koley et al. (7). Eight intestinal loops of about 10 cm, separated by uninoculated segments of 1 to 2 cm, were prepared in each animal. Test loops were inoculated with 1 ml of bacterial suspension containing approximately 109 cells. Negative-control loops were inoculated with 1 ml of phosphate-buffered saline. The loops were replaced in the peritoneal cavity, and the cavity was closed. After about 20 h the animal was sacrificed by intravenous injection of sodium pentobarbital and the loops were taken out. The volume of the accumulated fluid in ml and the length of the loop in cm were measured, and the extent of the fluid accumulation (FA) was expressed as ml/cm.All 19 strains of V. cholerae O1 El Tor variant belonged to the El Tor biotype as evident from phenotypic traits such as resistance to 50 units of polymyxin B and a positive Voges-Proskauer test (19). All harbored El Tor biotype-specific alleles of tcpA and rstR when examined as described previously (5, 6). The ctxB gene of all strains was of classical type by mismatch amplification mutation assay (MAMA)-PCR carried out as described by Morita et al. (8). Further, the CTB produced by all strains was confirmed to be the classical type by Western blotting by using monoclonal antibody against either classical CTB or El Tor CTB, which was prepared by immunizing rats with a synthesized peptide (either NTQIYTLNDKC for El Tor CTB or NTQIHTLNDKC for classical CTB). Approximately 50 to 100 ng of CT (measured by bead ELISA) in the culture supernatant of each strain was analyzed. The results of the Western blotting of a representative strain (strain AM157) are shown in Fig. Fig.11.Open in a separate windowFIG. 1.Results of Western blotting of the culture supernatant of a representative strain of El Tor variant biotype. Lanes 1 and 6, 100 ng of the purified classical CT; lanes 2 and 7, 100 ng of the purified El Tor CT; lanes 3 and 8, sample of El Tor variant strain AM157; lanes 4 and 9, sample of El Tor strain N16961; lanes 5 and 10, sample of classical strain L362. (A) Results with the monoclonal antibody against classical CTB. (B) Results with the monoclonal antibody against El Tor CTB. Numbers at left are molecular masses in kilodaltons (× 1,000).Figure Figure22 shows the distribution of the amounts of CT produced by strains examined. Each strain of El Tor variant, prototype El Tor, and classical biotype was cultured in 2 ml of AKI medium in a 10-ml test tube at 37°C for 20 h without shaking, and the supernatant of the culture was collected by centrifugation and was measured to determine the amount of CT by bead ELISA. It was found that most strains of El Tor variant produced much more CT than did most strains of prototype El Tor. All 19 El Tor variant strains produced more than 1,000 ng/ml/OD600 of CT, and among them 5 strains (AM157, 06-049, IDH60, BD200, and 06-098) produced more than 2,500 ng/ml/OD600, the highest (strain AM157) producing 4,656 ng/ml/OD600. The amount of CT produced varied but was not related to the year of isolation. Among 11 El Tor strains, 8 strains (V113, VC60, M14716, V7, VC64, V54, V24, and V32) produced less than 100 ng/ml/OD600, and among them 3 strains (V54, V24, and V32) produced less than 20 ng/ml/OD600. The rest of the strains (N16961, V100, and V114) produced more than 100 ng/ml/OD600, and the standard strain N16961 produced the largest amount (345 ng/ml/OD600). All 7 classical strains produced more than 900 ng/ml/OD600, and 2 of them (L362 and GP15) produced more than 2,000 ng/ml/OD600, the higher being L362 (3,028 ng/ml/OD600).Open in a separate windowFIG. 2.Amounts of CT produced by various biotypes of V. cholerae O1. Each circle represents an average of 4 determinations.The amount of CT produced was measured during the growth of the strains in AKI medium with the representative strains of El Tor variant, prototype El Tor, and classical biotype, and it was found that the differences in the amounts of CT produced among these 3 biotypes were observed from the beginning of the growth (early logarithmic phase) till the late stationary phase (data not shown).Table Table22 shows the mean CT amounts produced by the strains of different biotypes with standard deviations. The amount of CT produced by El Tor variant strains was about 20 times more than that produced by prototype El Tor strains, and it was more or less equivalent to that produced by classical strains. A difference in the CT production between El Tor variant strains and prototype El Tor strains was statistically analyzed by Microsoft Excel 2004 for Mac, the P value (Student t test) being <0.05.

TABLE 2.

Comparison of the amounts of CT produced by strains of various biotypes of V. cholerae O1a
Culture mediumCT concn (ng/ml/OD600)
El Tor variantEl TorClassical
AKI2,044.1 ± 966.891.3 ± 104.61,664.4 ± 782.0
Syncase81.3 ± 147.24.5 ± 3.7b114.7 ± 188.8
Open in a separate windowaStrains examined were as listed in Table Table11 unless indicated.bOnly 5 strains of El Tor biotype (N16961, V113, VC64, VC60, and V24) grew in Syncase medium cultured at 37°C with shaking.CT production by strains of El Tor variant, El Tor, and classical biotype was also examined when the strains were cultured in Syncase medium (2 ml in a 10-ml test tube) at 37°C for 20 h with shaking. As shown in Table Table2,2, although the amount of CT produced in Syncase medium was much smaller than that produced in AKI medium, El Tor variant strains produced much more CT than did El Tor strains and produced an amount more or less equivalent to that produced by classical strains. The P value (Student t test) of the difference in the amounts produced between El Tor variant strains and prototype El Tor strains analyzed by Microsoft Excel 2004 for Mac was <0.05.The ileal loop test was performed with a representative strain of El Tor variant (strain NLC41 producing 1,606 ng/ml/OD600 in AKI medium) together with representative strains of El Tor biotype (VC60 producing 60 ng/ml/OD600 in AKI medium) and classical biotype (L362 producing 3,028 ng/ml/OD600 in AKI medium). As shown in Table Table3,3, the FA ratio of the El Tor variant NLC41 was almost the same as that of classical strain L362. On the other hand, El Tor strain VC60 did not cause measurable fluid accumulation. This is most probably because the number of inoculated cells was not high enough. The numbers of V. cholerae organisms in the accumulated fluid (CFU/ml) and the amounts of CT in the loop (ng/ml and ng/CFU) were also measured, showing that the El Tor variant strain grew better than did the classical strain in the loop; thus, the amount of CT in the loop inoculated with the El Tor variant strain was larger than that in the loop inoculated with the classical strain. Measurement of CFU/ml of the accumulated fluid of the prototype of El Tor strain was not possible as no fluid accumulation occurred.

TABLE 3.

Results of rabbit ileal loop testd
BiotypeStrainFA (ml/cm)aCFU/mlbCT (ng/ml)aCT (ng/CFU)
El Tor variantNLC410.90 ± 0.291.0 × 1091,0061.006 × 10−6
El TorVC600c
ClassicalL3620.83 ± 0.381.6 × 10817.51.09 × 10−7
Open in a separate windowaAverages of 4 determinations (2 loops each in 2 rabbits).bAverages of 2 determinations (2 loops of 1 representative rabbit).c—, not applicable as no fluid accumulation occurred.dStatistical analysis (Student t test) was performed by Microsoft Excel 2004 for Mac.It is known that the clinical manifestation of cholera caused by classical strains is more severe than that caused by prototype El Tor strains (4). Although definite evidence to explain this is still not available, it has been hypothesized that a significant difference between the amounts of CT produced by these two biotype strains may reflect severity of clinical manifestation. If we were to accept the above hypothesis, a recent report by the World Health Organization (20) that the V. cholerae El Tor variant causes more severe episodes of cholera with higher case fatality rates might be explained by the results reported in this paper. However, Siddique et al. (16) reported that although El Tor variant strains appeared in 1998 in Bangladesh, the greater severity of cholera became evident only around 2006. Therefore, they concluded that it is not clear whether the observed higher proportion of severe dehydration is due to El Tor variants. Further study is needed to elucidate the role of CT produced by El Tor variant strains in the clinical manifestation of infection.  相似文献   
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