全文获取类型
收费全文 | 7001篇 |
免费 | 451篇 |
国内免费 | 20篇 |
专业分类
耳鼻咽喉 | 31篇 |
儿科学 | 214篇 |
妇产科学 | 181篇 |
基础医学 | 1156篇 |
口腔科学 | 77篇 |
临床医学 | 777篇 |
内科学 | 1299篇 |
皮肤病学 | 192篇 |
神经病学 | 647篇 |
特种医学 | 152篇 |
外科学 | 642篇 |
综合类 | 94篇 |
一般理论 | 4篇 |
预防医学 | 900篇 |
眼科学 | 179篇 |
药学 | 388篇 |
中国医学 | 19篇 |
肿瘤学 | 520篇 |
出版年
2023年 | 64篇 |
2022年 | 84篇 |
2021年 | 194篇 |
2020年 | 110篇 |
2019年 | 145篇 |
2018年 | 181篇 |
2017年 | 138篇 |
2016年 | 176篇 |
2015年 | 192篇 |
2014年 | 265篇 |
2013年 | 384篇 |
2012年 | 476篇 |
2011年 | 564篇 |
2010年 | 289篇 |
2009年 | 271篇 |
2008年 | 471篇 |
2007年 | 431篇 |
2006年 | 440篇 |
2005年 | 464篇 |
2004年 | 393篇 |
2003年 | 371篇 |
2002年 | 327篇 |
2001年 | 83篇 |
2000年 | 67篇 |
1999年 | 62篇 |
1998年 | 70篇 |
1997年 | 59篇 |
1996年 | 49篇 |
1995年 | 44篇 |
1994年 | 41篇 |
1993年 | 47篇 |
1992年 | 37篇 |
1991年 | 30篇 |
1990年 | 28篇 |
1989年 | 21篇 |
1988年 | 27篇 |
1987年 | 16篇 |
1986年 | 17篇 |
1985年 | 22篇 |
1984年 | 25篇 |
1983年 | 20篇 |
1982年 | 25篇 |
1981年 | 13篇 |
1980年 | 16篇 |
1979年 | 13篇 |
1978年 | 13篇 |
1976年 | 17篇 |
1975年 | 24篇 |
1974年 | 15篇 |
1973年 | 19篇 |
排序方式: 共有7472条查询结果,搜索用时 15 毫秒
91.
92.
Isao Ohsawa Daisuke Honda Yusuke Suzuki Tomoo Fukuda Keisuke Kohga Eishin Morita Shinichi Moriwaki Osamu Ishikawa Yoshihiro Sasaki Masaki Tago Greg Chittick Melanie Cornpropst Sharon C. Murray Sylvia M. Dobo Eniko Nagy Sharon Van Dyke Lacy Reese Jessica M. Best Heather Iocca Phil Collis William P. Sheridan Michihiro Hide 《Allergy》2021,76(6):1789-1799
93.
Andrea Sánchez Paulina Bustos Paula Honorato Carlos F. Burgos Natalia Barriga Cinthia E. Jannes Katia Sáez Rodrigo Alonso Sylvia Asenjo Claudia Radojkovic 《Journal of clinical lipidology》2021,15(2):366-374.e1
BackgroundFamilial hypercholesterolemia (FH) is an inherited disorder mainly caused by mutations in the LDL receptor (LDL-R) and characterized by elevation of low-density lipoprotein cholesterol (LDL-C) levels and premature cardiovascular disease.ObjectiveIn this study, we evaluated the clinical phenotype of the p.Asp47Asn, described as an uncertain pathogenic variant, and its effect on the structure of LDL-R and ligand interactions with apolipoproteins.Methods27 children and adolescents with suspected FH diagnosis were recruited from a pediatric endocrinology outpatient clinic. Blood samples were collected after 12 h fasting for lipid profile analysis. DNA sequencing was performed for six FH-related genes by Ion Torrent PGM platform and copy number variation by MLPA. For index cases, a familial cascade screening was done restricted to the same mutation found in the index case. In silico analysis were developed to evaluate the binding capacity of LDL-R to apolipoproteins B100 and E.ResultsLipid profile in children and adolescents demonstrated higher LDL-C levels in p.Asp47Asn carriers compared to the wild type genotype. In silico analysis predicted a reduction in the binding capacity of the ligand-binding modules LA1-2 of p.Asp47Asn LDL-R for ApoB100 and ApoE, which was not produced by local structural changes or folding defects but as a consequence of a decreased apparent affinity for both apolipoproteins.ConclusionThe clinical phenotype and the structural effects of p.Asp47Asn LDL-R mutation suggest that this variant associates to FH. 相似文献
94.
95.
96.
97.
98.
Sylvia M. LaCourse Raquel M. Martinez David H. Spach Ferric C. Fang 《The American journal of tropical medicine and hygiene》2015,92(3):599-600
Cochliomyia hominivorax, the New World screwworm, was a serious livestock pest in the southern United States until the 1960s, when it was successfully eradicated by the release of sterile male flies. It remains endemic in parts of the Caribbean and South America, and there is concern that climate change may extend its geographic distribution. Cochliomyia hominivorax is voracious and can cause extensive damage to soft tissue and bone. We describe the case of a 26-year-old traveler who presented with otalgia and bloody otorrhea after returning from a vacation in the Dominican Republic, where exposure to screwworm flies most likely occurred during a nap on the beach. The causative agent was recognized by its characteristic larval anatomy, which includes pigmented dorsal tracheal trunks and posterior spiracles with an open peritreme.A 26-year-old female presented with a 2-day history of otalgia and bloody otorrhea after returning from a week of vacation in the Dominican Republic, where she stayed in a beachside resort with screened windows, swam in the ocean, hiked near an estuary, and sunbathed on the beach. She admitted to falling asleep on the beach one evening after drinking alcohol. The next day she had right ear discomfort with the sensation of movement, and removed a fly from her ear. One day later during the flight home, she had acute onset of ear pain, which she initially attributed to pressure changes associated with her flight, until she began noting discharge from the ear. The discharge was initially clear but became bloody within 1–2 hours. She sought medical care the next day, when an otoscopic examination revealed multiple motile larvae (Figure 1, Panel A). She was immediately referred to an otolaryngologist who performed excision and debridement of her external auditory canal with atticotomy.Open in a separate windowFigure 1.Panel A: Excised tissue displaying multiple motile larvae that were removed from the external auditory canal of a returning traveler vacationing in the Dominican Republic with auricular myiasis. Panel B: The characteristic pigmented dorsal tracheal trunks (white open arrow) and posterior spiracles with an open peritreme (gray closed arrow and inset) of Cochliomyia hominivorax.Intraoperative findings revealed soft tissue larval infiltration extending to the temporal bone and tympanic membrane perforation without middle ear involvement. The patient tolerated the debridement well and was prescribed amoxicillin-clavulanic acid for potential secondary soft-tissue infection. She subsequently underwent tympanoplasty with a split-thickness skin graft. The removed larvae were preliminarily identified as Cochliomyia hominivorax by the University of Washington Microbiology Laboratory on the basis of characteristic anatomic findings. Definitive identification was confirmed by the U.S. Department of Agriculture Screwworm Research Unit.Cochliomyia hominivorax (“human eater”), the New World screwworm, has smooth larvae with pigmented dorsal tracheal trunks (white open arrow) and posterior spiracles with an open peritreme (gray closed arrow, and inset) (Figure 1, Panel B).1 The larvae feed on the living tissue of warm-blooded mammals using sharp hook-like mandibles (Supplemental Video). Spines found in concentric rings along the larvae resemble a screw and aid in anchoring the larvae within tissue, hence the name “screwworm.”2 A female adult can lay hundreds of eggs at one time, often within existing open wounds.3 The voracious larvae emerge within 24 hours and can cause extensive soft tissue damage, and in some cases, destruction of bone. After 5–7 days the pupae mature and attempt to leave the wound to eventually burrow into the ground to pupate.2 Adult flies can live for 2–3 weeks. Female flies are attracted to the scent of normal secretions of the orifices of mammals, with case reports describing infestation of the ears, eyes, nose, mouth, vagina, and rectum,4 and are able to fly great distances (∼50 km/week) to find a suitable host in which to deposit their eggs.2 The scent of tissue infested with C. hominivorax can attract additional adult female flies that deposit their eggs within the same site. Individuals who are immobile, developmentally delayed, mentally ill, or alcoholic are at a higher risk of infestation.3 Orbital myiasis can be particularly devastating, requiring extensive debridement and sometimes enucleation.4 Several case reports have described secondary myiasis of ulcerative cutaneous malignancies.5 Auricular myiasis, as observed in our patient, is extremely rare and primarily occurs in children.3 Treatment of New World screwworm infestation consists of debridement, antibiotics if evidence of secondary infection is present, and adjunctive ivermectin in severe cases.4Cochliomyia hominivorax was formerly endemic in the southern United States where it was responsible for a serious economic burden caused by livestock destruction, until the 1960s when it became the first pest to be successfully eradicated by the release of sterile male flies.6 The New World screwworm remains endemic in parts of the Caribbean and South America, and there is concern that climate change may extend its geographic distribution.7 Since the New World screwworm has been eradicated from the United States for decades, clinicians may be unaware of this potentially devastating infestation resulting from foreign travel to endemic areas. As a result of the risk for significant tissue destruction, particularly if diagnosis is delayed, it is important for clinicians to be able to promptly recognize and appropriately treat this form of myiasis. 相似文献
99.
100.
Diastolic dysfunction is increasingly recognized as a cause of hemodynamic instability in the perioperative setting. Difficulty weaning from cardiopulmonary bypass and an increased need for inotropic support can occur in the absence of systolic impairment. Diastolic dysfunction can also impede hemodynamic stabilization and weaning progress in the mechanically ventilated critically ill patient. The use of transesophageal echocardiography in the ICU can assist in diagnosing the presence and progression of diastolic impairment, which may help to target therapeutic interventions that lead to positive outcomes. This review summarizes the conventional and new echocardiographic modalities for evaluating diastolic function in the perioperative setting. 相似文献