首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   150篇
  免费   1篇
耳鼻咽喉   1篇
儿科学   2篇
妇产科学   4篇
基础医学   20篇
口腔科学   4篇
临床医学   14篇
内科学   30篇
皮肤病学   4篇
神经病学   12篇
特种医学   2篇
外科学   18篇
综合类   1篇
预防医学   10篇
眼科学   8篇
药学   15篇
中国医学   1篇
肿瘤学   5篇
  2023年   6篇
  2022年   15篇
  2021年   19篇
  2020年   5篇
  2019年   8篇
  2018年   10篇
  2017年   7篇
  2016年   4篇
  2015年   3篇
  2014年   15篇
  2013年   6篇
  2012年   5篇
  2011年   5篇
  2010年   2篇
  2009年   6篇
  2008年   1篇
  2007年   4篇
  2006年   3篇
  2005年   2篇
  2004年   6篇
  2003年   2篇
  2002年   1篇
  2001年   2篇
  2000年   2篇
  1999年   5篇
  1996年   2篇
  1995年   1篇
  1990年   1篇
  1988年   1篇
  1983年   1篇
  1981年   1篇
排序方式: 共有151条查询结果,搜索用时 14 毫秒
51.
52.
《Revue neurologique》2022,178(9):932-938
BackgroundUntil recently, few therapeutic options, other than symptomatic treatment, were available for patients with primary progressive multiple sclerosis (PPMS). Ocrelizumab is the only approved treatment in this indication, and only since 2017. However, many patients in France are receiving off-label treatments for PPMS, mainly rituximab, mycophenolate mofetil, methotrexate, cyclophosphamide, and azathioprine.ObjectiveTo evaluate published data concerning the efficacy of these five treatments frequently used as off-label disease-modifying therapies.MethodsWe reviewed and summarized the studies published in Pubmed since the inception of the database.ResultsEvidence from randomized controlled trials is lacking to support the use of these treatments as disease-modifying therapies in PPMS.ConclusionThe literature lacks dedicated studies to support the off-label use of these disease-modifying therapies in PPMS. However, some limited data are available in the literature suggesting that the use of rituximab and cyclophosphamide could potentially be of some interest in specific subpopulations.  相似文献   
53.
54.
55.
56.
57.
58.
The pseudosyndrome of Meigs is caracterised by a triad, which associates a solid benign tumor of the ovary, an ascitis and a pleural effusion. Surgical extraction of the tumor entails disappearance of the symptomatology. The authors report in this study a case of an ovarian goitre revealed by this syndrom.  相似文献   
59.
60.
ObjectiveThis work compares the virulence between pigmented (P) and albino (A) filamentous forms of S. schenckii through experimental skin sporotrichosis.Material and methodsTwo original wild pigmented isolates (1 and 2) cultivated in yeast extract peptone dextrose (YEPD), were exposed to 300 erg/mm2 of UV radiation in order to produce mutant albinos. Swiss albino mice were divided in four groups (P1, A1, P2 and A2) and inoculated in the right paw pad with 0.1 ml of solution (1 × 106cells/ml) and observed during nine weeks.ResultsThe albino groups A1 (86%) and A2 (100%) presented intense inflammatory reactions in the inoculation point (p < 0.01) in Week 2 after inoculation, while in the pigmented groups, around 70% of the animals presented multiple skin lesions in Week 4 (p < 0.01). In the last three weeks of the experiment, 67% of the mice in group P1 demonstrated multiple skin lesions. S. schenckii was recovered from samples obtained in necropsy and the histological analysis revealed formation of granulomas with yeast-like cells in the central area of the lesion.ConclusionThe results obtained in this experimental model permit the conclusion that there are virulence differences between pigmented and mutant albino isolates of S. schenckii in the development of experimental skin sporotrichosis.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号