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1.
《Neuro-Chirurgie》2022,68(3):262-266
BackgroundThe prognosis for patients with recurrent glioblastoma (GBM) is dismal, and the question of repeat surgery at time of recurrence is common. Re-operation in the management of these patients remains controversial, as there is no randomized evidence of benefit. An all-inclusive pragmatic care trial is needed to evaluate the role of repeat resection.Methods3rGBM is a multicenter, pragmatic, prospective, parallel-group randomized care trial, with 1:1 allocation to repeat resection or standard care with no repeat resection. To test the hypothesis that repeat resection can improve overall survival by at least 3 months (from 6 to 9 months), 250 adult patients with prior resection of pathology-proven glioblastoma for whom the attending surgeon believes repeat resection may improve quality survival will be enrolled. A surrogate measure of quality of life, the number of days outside of hospital/nursing/palliative care facility, will also be compared. Centers are invited to participate without financial compensation and without contracts. Clinicians may apply to local authorities to approve an investigator-led in-house trial, using a common protocol, web-based randomization platform, and simple standardized case report forms.DiscussionThe 3rGBM trial is a modern transparent care research framework with no additional risks, tests, or visits other than what patients would encounter in normal care. The burden of proof remains on repeat surgical management of recurrent GBM, because this management has yet to be shown beneficial. The trial is designed to help patients and surgeons manage the uncertainty regarding optimal care.Clinical Trial Registrationhttp://www.clinicaltrials.gov. Unique identifier: NCT04838782. 相似文献
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Sathiyavelavan Gopalan Jagadesh Chandra Bose S. Periasamy 《The Indian journal of surgery》2015,77(3):232-236
The aim of this study is to review the literature to find out the exact etiology of anastomotic cancers of colon post resection and differentiate them between a recurrence, second primary, and metastatic disease (local manifestation of systemic disease). Web-based literature search was done, and datas collected. We searched PubMed for papers using the keywords colon cancer recurrence, anastomotic recurrence, and recurrent colon carcinoma. We also searched for systematic review in the same topic. In addition, we used our personal referrence archive. Anastomotic recurrences of colon are postulated to arise due to inadequate margins, tumor implantation by exfoliated cells, altered biological properties of bowel anastomosis, and missed synchronous lesions. Some tumors are unique with repeated recurrence after repeated resection. Duration after primary surgery plays a major role in differentiating recurrent and second primary lesions. Repeated recurrences after repeated resections have to be considered a manifestation of systemic disease or metastatic disease due to the virulence of the disease. A detailed analysis and study of patients with colonic anastomotic lesion are required to differentiate it between a recurrent, a second primary lesion, and a metastatic disease (local manifestation of a systemic disease). The nomenclature is significant to study the survival of these patients, as a second primary lesion will have different survival compared to that of recurrent lesions. 相似文献
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Heubner回返动脉显微外科解剖及其临床应用 总被引:2,自引:0,他引:2
目的 :为前交通动脉复合体部位显微手术避免损伤Heubner回返动脉提供相关的应用解剖学资料。方法 :对经双侧椎动脉 (VA)、颈内动脉 (ICA)乳胶灌注的尸头标本 2 2例 ,按翼点入路方向 ,在手术显微镜下解剖观测 2 0例Heubner回返动脉的起点、管径、行径及其毗邻关系。 2例模拟手术操作。结果 :(1)本组观测到 4 3支回返动脉 ,其中 39支Heubher回返动脉 ;4支副Heubner回返动脉。 (2 )Heubner回返动脉 4 6 .5 % (2 0 / 4 3)起于A2 段 ,2 5 .6 % (11/ 4 3)起于A1段 ,2 7.9% (12 /4 3)起于前交通动脉 (ACOA)水平的大脑前动脉 (ACA)。 (3)Heubner回返动脉起点管径 :左侧 0 .81± 0 .2 1mm(0 .35~ 1.17mm) ;右侧 0 .84± 0 .2 6mm(0 .37~ 1.2 1mm)。 (4 )回返动脉发出后 ,与ACA反方向成锐角 ,沿A1上壁、外侧及后内侧 ,越过ICA两分叉 ,经大脑中动脉 (MCA)始段前面穿通入脑 ,少数回返动脉行走于前穿质 (APS)的后部。A1近端 3~ 5mm或中 1/ 3段穿通支少。结论 :在前交通动脉复合体部位手术时 ,A1近端 3~ 5mm或中 1/ 3段夹闭 ,并解剖寻找、剥离Heubner回返动脉 ,可避免损伤Heubner回返动脉及其它穿通支 ,最大限度减少术后并发症 相似文献
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目的研究创伤性复发性腓骨肌腱脱位的手术方法. 方法回顾分析1986年1月~2003年12月手术治疗的21例创伤性复发性腓骨肌腱脱位的病例,所有病例均应用Watson Jones手术. 结果 15例得到随访,随访时间1~15年,平均4.9年.1例因外伤再次脱位,其余14例未再出现脱位,均恢复正常运动或训练,比赛. 结论 Watson Jones手术治疗复发性脱位操作简单,损伤小,效果满意. 相似文献
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MRI诊断腰椎间盘术后粘连和突出复发 总被引:2,自引:0,他引:2
失败的下腰椎手术是个复杂的问题,由于其症状和体征不典型,单靠临床检查很难明确诊断,而脊髓造影和常规CT等检查也很难区别突出复发和硬膜外粘连。本文分析了32例再手术患者MRI图象,并与第二次手术所见对比,发现27例MRI诊断准确,3例假阳性,2例因信号缺失不能明确诊断。 相似文献
9.
J. Dörr F. J. Dieste D. Klaasen van Husen F. Zipp H. P. Vogel 《Neurological sciences》2006,27(6):424-425
Abstract Miller Fisher syndrome (MFS) is a rare and usually monophasic polyradiculoneuropathy characterised by ophthalmoplegia, decreased
or absent tendon reflexes, and ataxia. The objective of this study was to report a case of recurrent MFS with a clinical presentation
virtually indistinguishable from botulism. The patient was a young man with two episodes of increasing external ophthalmoplegia,
ptosis, and ataxia with a long asymptomatic interval in between. The second episode occurred after consumption of rotten fish
and was accompanied by gastrointestinal symptoms and an anticholinergic syndrome. Very rarely, MFS can present with a recurrent
course. The importance of this case of recurrent MFS lies not only in its long asymptomatic period and identical clinical
presentation, but also in its instructiveness regarding the differential diagnosis of MFS, particularly life-threatening botulism. 相似文献
10.
T K Al-Hussaini D M Abd el-Aal I B Van den Veyver 《International journal of gynaecology and obstetrics》2003,83(2):179-186
OBJECTIVES: To present a series of women with recurrent molar pregnancies, including rare familial cases, and discuss etiology and treatment options. METHODS: We performed a detailed clinical evaluation and pedigree analysis of five Egyptian women with recurrent pregnancy loss due to molar pregnancy. RESULTS: The women had a history of four to nine consecutive hydatidiform moles but of no viable pregnancies. Two of the women had molar pregnancies with different husbands who themselves had viable offspring from previous wives; and three of them, who belonged to a family with extensive intermarriage, had a pedigree consistent with an autosomal recessive maternal-effect mutation. CONCLUSIONS: Recurrent pregnancy loss due to habitual molar pregnancy is uncommon and familial cases are extremely rare. The etiology of this disorder is not well understood but likely results from a maternal-effect mutation. Management options are limited, especially for couples who desire to have their own genetic offspring. 相似文献