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1.
Time allocation studies show that women in developing countriesface severe time constraints. However, such studies give a lessclear picture of the time women spend on health and child carein the home and utilization of health services because theseare primarily sporadic, not daily, activities. Reporting timespent by women on illness or health care utilization as a dailyaverage masks the true cost of periodically losing half of aday or more of work time. Almost no direct empirical data have been gathered on the timecosts to women of breastfeeding, immunizations, ORT, or growthmonitoring, nor on whether time costs are an important determinantof utilization of these technologies. Specific research designedaround the introduction of child survival projects, plus theinclusion of appropriate measures in the evaluations of ongoingprojects, could fill this gap. Even without further research,recognition of the time constraints faced by low-income mothersin conjunction with lessons learned from successful growth monitoringand immunization projects suggests that outreach efforts maybe an important key to increasing utilization of child survivaltechnologies. 相似文献
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J. D. ARNOLD G. I. LESLIE G. WILLIAMS P. RACK M. SILINK 《Journal of paediatrics and child health》1987,23(4):227-229
Adrenocortical responsiveness was assessed in eight very low birthweight neonates who had bronchopulmonary dysplasia and had been weaned from mechanical ventilation using dexamethasone. Three of the eight infants did not respond to ACTH stimulation during the first week after cessation of dexamethasone, but all three responded normally when retested at least 1 month later. The present authors have thus demonstrated that some infants have at least temporary adrenocortical unresponsiveness after prolonged courses of glucocorticoid therapy, and suggest that adrenocortical function should be assessed in all infants who are weaned from mechanical ventilation using dexamethasone. 相似文献
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PETER R. BRAUDE LESLIE D. ROSS VIRGINIA N. BOLTON KIM OCKENDEN 《BJOG : an international journal of obstetrics and gynaecology》1987,94(1):76-83
Summary. Retrograde ejaculation is an uncommon but treatable form of male infertility. Successful recovery of live spermatozoa from the post-ejaculatory urine for artificial insemination is dependent on careful regulation of pH and osmolarity of the urine into which ejaculation takes place, and separation of the motile spermatozoa from the debris and cells which are found in these samples. Three pregnancies established by artificial insemination of spermatozoa recovered by non-invasive means from the bladders of men suffering from retrograde ejaculation are described. The techniques for preparing the urine for spermatozoal survival, and for removal of cells and debris by sedimentation or buoyant density centrifugation are discussed. 相似文献
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J. M. SMITH M. F. JAMES K. H. J. BOCKHORST M. I. SMITH D. P. BRADLEY N. G. PAPADAKIS T. A. CARPENTER A. A. PARSONS R. A. LESLIE L. D. HALL C. L.‐H. HUANG 《Journal of anatomy》2001,198(5):537-554
Cortical spreading depression (CSD) and peri‐infarct depolarisation (PID) are related phenomena that have been associated with the human clinical syndromes of migraine (CSD), head injury and stroke (PID). Nevertheless the existence of CSD in man remains controversial, despite the detection of this phenomenon in the brains of most, if not all, other animal species investigated. This failure to unambiguously detect CSD clinically may be at least partly due to the anatomically complex, gyrencephalic structure of the human brain. This study was designed to establish conditions for the study of CSD in the brain of a gyrencephalic species using the noninvasive technique of magnetic resonance imaging (MRI). The 3‐dimensional (3D) gyrencephalic anatomy of the cat brain was examined to determine the imaging conditions necessary to detect CSD events. Orthogonal transverse, sagittal and horizontal T1‐weighted image slices showed that the marginal and suprasylvian gyri were the most appropriate cortical structures to study CSD. This was in view of (1) their simple geometry: (2) their lengthy extent of grey matter orientated rostrocaudally in the cortex: (3) their separation by a sulcus across which CSD spread could be studied and (4) the discontinuity in the grey matter in these regions between the right and left hemispheres dorsal to the corpus callosum. The structure suggested by the T1‐weighted images was corroborated by systematic diffusion tensor imaging to map the fractional anisotropy and diffusion trace. Thus a single horizontal image plane could visualise the neighbouring suprasylvian and marginal gyri of both cerebral hemispheres, whereas its complex shape and position ruled out the ectosylvian gyrus for CSD studies. With the horizontal imaging plane, CSD events were reproducibly detected by animating successive diffusion‐weighted MR images following local KCl stimulation of the cortical surface. In single image frames, CSD detection and characterisation required image subtraction or statistical mapping methods that, nevertheless, yielded concordant results. In repeat experiments, CSD events were qualitatively similar in appearance whether elicited by sustained or transient KCl applications. Our experimental approach thus successfully describes cat brain anatomy in vivo, and elucidates the necessary conditions for the application of MRI methods to detect CSD propagation. 相似文献
7.
ERIKA J. Douglass LESLIE T. COOPER A. CAROLINA MORALES-LARA DEMILADE A. ADEDINSEWO TODD D. ROZEN LORI A. BLAUWET DELISA FAIRWEATHER 《Journal of cardiac failure》2021,27(2):132-142
BackgroundThe incidence of peripartum cardiomyopathy (PPCM) is known through referral center databases that may be affected by referral, misclassification, and other biases. We sought to determine the community-based incidence and natural history of PPCM using the Rochester Epidemiology Project.Methods and ResultsIncident cases of PPCM occurring between January 1, 1970, and December 31, 2014, were identified in Olmsted County, Minnesota. A total of 15 PPCM cases were confirmed yielding an incidence of 20.3 cases per 100,000 live births in Olmsted County, Minnesota. Clinical information, disease characteristics, and outcomes were extracted from medical records in a 27-county region of the Rochester Epidemiology Project including Olmsted County and matched in a 1:2 ratio with pregnant women without PPCM. A total of 48 women were identified with PPCM in the expanded 27-county region. There was 1 death and no transplants over a median of 7.3 years of follow-up. Six of the 23 women with subsequent pregnancies developed recurrent PPCM, all of whom recovered. Migraine and anxiety were identified as novel possible risk factors for PPCM.ConclusionsThe population-based incidence of PPCM was 20.3 cases per 100,000 live births in Olmsted County, Minnesota. Cardiovascular outcomes were generally excellent in this community cohort. 相似文献
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ALLISON BRASHEAR JONATHAN W MINK DEBORAH F HILL NIKI BOGGS W VAUGHN MCCALL MARK A STACY BEVERLY SNIVELY LANEY S LIGHT KATHLEEN J SWEADNER LAURIE J OZELIUS LESLIE MORRISON 《Developmental medicine and child neurology》2012,54(11):1065-1067
We report new clinical features of delayed motor development, hypotonia, and ataxia in two young children with mutations (R756H and D923N) in the ATP1A3 gene. In adults, mutations in ATP1A3 cause rapid‐onset dystonia–Parkinsonism (RDP, DYT12) with abrupt onset of fixed dystonia. The parents and children were examined and videotaped, and samples were collected for mutation analysis. Case 1 presented with fluctuating spells of hypotonia, dysphagia, mutism, dystonia, and ataxia at 9 months. After three episodes of hypotonia, she developed ataxia, inability to speak or swallow, and eventual seizures. Case 2 presented with hypotonia at 14 months and pre‐existing motor delay. At age 4 years, he had episodic slurred speech, followed by ataxia, drooling, and dysarthria. He remains mute. Both children had ATP1A3 gene mutations. To our knowledge, these are the earliest presentations of RDP, both with fluctuating features. Both children were initially misdiagnosed. RDP should be considered in children with discoordinated gait, and speech and swallowing difficulties. 相似文献