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1.
Limited-field-of-view radio-frequency receiver antennas provide improved near-field sensitivity for magnetic resonance imaging by decreasing the antenna volume. The Helmholtz-type surface coil, consisting of two flat rings, is an organ-encompassing antenna that takes advantage of this principle to yield an improved signal-to-noise ratio (S/N). The coil was tested in a group of 50 patients and 16 healthy volunteers. Images obtained with the Helmholtz coil demonstrated quantitatively superior S/N of 2.2-fold or greater than that of comparison body coil images, as well as qualitatively superior anatomic resolution. 相似文献
2.
Genetic hypothyroid mice: normal cerebellar morphology but altered glycerol-3-phosphate dehydrogenase in Bergmann glia 总被引:2,自引:0,他引:2
The present study was undertaken to investigate the effects of thyroid deficiency on cerebellar development with mouse endocrine genetic models. Four types of mutant mice, the growth hormone- and thyroid hormone-deficient Snell dwarf mouse (dw/dw), the growth hormone-deficient little mouse (lit/lit), the primary hypothyroid mouse (hyt/hyt), and the congenital genital goiter mouse (cog/cog) were analyzed for expression of the glial enzyme marker glycerol-3-phosphate dehydrogenase (GPDH) and several other marker proteins. GPDH expression, as determined by enzyme activity and Northern blot analysis, was reduced by about 50% in the cerebellum and brainstem of the three hypothyroid mutant mice. No reduced expression was found in any region of the brain of the growth hormone-deficient lit/lit mutant. Visualization of GPDH by immunohistology showed that the immunoreactive enzyme was strikingly reduced in the Bergmann glial cells of dw/dw, hyt/hyt, and cog/cog mutant mice, particularly in the radial glial processes. To evaluate the specificity of the effect on GPDH expression, we also examined the expression of the glial cell-specific S-100 protein by immunohistology. In all mutant cerebella, both the intensity and pattern of staining of the Bergmann glial cells were indistinguishable from that of normal controls, suggesting that the Bergmann glial cells are morphologically normal in the hypothyroid mice. The morphology of the Purkinje cell neurons was similarly visualized by immunohistology using an antiserum specific for the microtubule-associated proteins. Surprisingly, the morphology of the Purkinje cell dendritic arborization also appeared unaltered in the hypothyroid mice. The results suggest that the morphological development of the mouse cerebellum is relatively unaffected by hypothyroidism.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
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WG Mitchell H Lynn JF Bale MA Maeder SM Donfield B Garg AH Tilton JK Willis TP Bohan 《Pediatrics》1997,100(5):817-824
BACKGROUND: Boys and young men with hemophilia treated with factor infusions before 1985 had a substantial risk of acquiring the human immunodeficiency virus (HIV) and the acquired immunodeficiency syndrome. This study was designed to assess the effects of HIV and hemophilia per se on neurological function in a large cohort of subjects with hemophilia, and to investigate the relationships between neurological disease and death during follow-up. METHODS: Three hundred thirty-three boys and young men (207 HIV seropositive and 126 HIV seronegative) were evaluated longitudinally in a multicenter, multidisciplinary study. Neurological history and examination were conducted at baseline and annually for 4 years. The relationship between neurological variables, HIV serostatus, CD4+ cell counts, and vital status at the conclusion of the study was examined using logistic regression models. RESULTS: The risks of nonhemophilia-associated muscle atrophy, behavior change, and gait disturbance increased with time in immune compromised HIV-seropositive subjects compared with HIV seronegative or immunologically stable HIV-seropositive subjects. The risk of behavior change in immune compromised HIV-seropositive hemophiliacs, for example, rose to 60% by year 4 versus 10% to 17% for the other study groups. Forty-five subjects (13.5%), all of whom were HIV seropositive, died by year 4. Subjects who died had had increased risks of hyperreflexia, nonhemophilia-associated muscle atrophy, and behavior change. CONCLUSIONS: These results indicate that immune compromised, HIV-seropositive hemophiliacs have high rates of neurological abnormalities over time and that neurological abnormalities were common among subjects who later died. By contrast, immunologically stable HIV-seropositive subjects did not differ from the HIV-seronegative participants. Hemophilia per se was associated with progressive abnormalities of gait, coordination, and motor function. 相似文献
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M. H. F. Friedman Helen Battle Ivan Bennett Wm. D. Beamer J. Edward Berk J. B. Bernstine G. P. Blundell F. X. Chockly H. W. Davenport S. A. Friedman Carmella Foderaro J. L. Garcia Oller J. Logan Irvin D. L Klein G. Klenner Edgar D. Knerr S. A. Komarov Harry Metzger J. M. McGeehan M. J. Oppenheimer Karl E. Paschkis I. J. Pincus R. J. Revelli B. C. Riggs Frederick H. Scharles James P. Schooley H. Siplet G. W. Stavraky I. M. Theone G. A. H. Tice Adolph A. Walkling D. A. Wocker 《The American journal of digestive diseases》1944,11(1):24-30
7.
M. H. F. Friedman D. J. Abolofia B. R. Adolph Helen Battle Wm. D. Beamer Ivan Bennett J. Edward Berk J. B. Bernstine G. P. Blundell R. L. Burdick R. E. Capps F. X. Chockley C. G. Clements John J. Cox H. W. Davenport E. R. Feaver Carmela Forderaro S. A. Friedman J. Logan Irvin G. Klenner Edgar G. Knerr S. A. Komarov Harry Metzger M. J. Oppenheimer K. E. Paschkis I. J. Pincus B. C. Riggs F. E. St. George Frederick H. Scharles N. M. Small G. N. N. Smith Wm. J. Snape G. W. Stavraky Horace Stilyung I. M. Theone C. A. H. Tice Adolph A. Walkling D. A. Wocker 《The American journal of digestive diseases》1945,12(11):383-384
8.
M. H. F. Friedman D. J. Abolofia B. R. Adolph Helen Battle WM. D. Beamer Ivan Bennett J. Edward Berk J. B. Bernstine G. P. Blundell R. L. Burdick R. E. Capps F. X. Chockley C. G. Clements John J. Cox H. W. Davenport E. R. Feaver Carmela Forderaro S. A. Friedman J. Logan Irvin G. Klenner Edgar G. Knerr S. A. Komarov Harry Metzger M. J. Oppenheimer K. E. Paschkis I. J. Pincus B. C. Riggs F. E. St. Georce Frederick H. Scharles N. M. Small G. N. N. Smith WM. J. Snape G. W. Starvraky Horace Stilyung I. M. Theone C. A. H. Tice Adolph A. Walkling D. A. Wocker 《The American journal of digestive diseases》1945,12(8):276-280
9.
Induction of proliferation of B prolymphocytic leukemia cells by phorbol ester and native or recombinant interferon-gamma 总被引:1,自引:0,他引:1
Phorbol ester phorbol myristate acetate (PMA) induces proliferation in nonmalignant human B cells and B cells from a patient with B prolymphocytic leukemia (B-PLL). Mitogen-free T cell-derived conditioned medium acts synergistically with PMA in inducing proliferation of B-PLL cells but does not enhance the PMA-stimulated outgrowth of nonmalignant B cells. Interleukin 2 (IL-2) has no effect on the outgrowth of B-PLL cells, and monoclonal antibodies against the IL-2 receptor do not influence the response to PMA and conditioned medium. Recombinant interferon-gamma (IFN-gamma), in contrast, is a potent enhancer of PMA-induced proliferation of B-PLL cells. With gel filtration techniques and with the use of anti-IFN-gamma antibodies, it is shown that IFN-gamma in the conditioned medium is responsible for the observed increase in B-PLL cell proliferation. Preincubation of B- PLL cells with IFN-gamma induces responsiveness to PMA, whereas IFN- gamma alone had no effect on these cells when pretreated with PMA. The combined data show that, in the presence of PMA, native and recombinant IFN-gamma are growth factors for B cells from a B-PLL patient and that IL-2 is not involved in this process. 相似文献
10.
M H. F. Friedman Helen Battle Ivan Bennett Wm. D. Beamer J. Edward Berk J. B. Bernstine G. P. Blundell F. X. Chockly H. W. Davenport S. A. Friedman Carmella Foderaro J. L. Garcia Oller J. Logan Irvin D. L. Klein G. Klenner Edgar D. Knerr S. A. Komarov Harry Metzger J. M. Mcgeehan M. J. Oppenheimer Karl E. Paschkis I. J. Pincus R. J. Revelli B. C. Riggs Frederick H. Scharles James P. Schooley H. Siplet G. W. Stavraky I. M. Theone G. A. H. Tice Adolph A. Walkling D. A. Wocker 《The American journal of digestive diseases》1944,11(7):234-240