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   1489篇
  免费   124篇
  国内免费   3篇
耳鼻咽喉   16篇
儿科学   42篇
妇产科学   20篇
基础医学   219篇
口腔科学   5篇
临床医学   107篇
内科学   349篇
皮肤病学   26篇
神经病学   132篇
特种医学   16篇
外科学   153篇
综合类   56篇
一般理论   2篇
预防医学   85篇
眼科学   83篇
药学   188篇
中国医学   10篇
肿瘤学   107篇
  2023年   8篇
  2022年   30篇
  2021年   36篇
  2020年   21篇
  2019年   30篇
  2018年   28篇
  2017年   19篇
  2016年   38篇
  2015年   47篇
  2014年   36篇
  2013年   67篇
  2012年   72篇
  2011年   82篇
  2010年   52篇
  2009年   50篇
  2008年   59篇
  2007年   65篇
  2006年   84篇
  2005年   77篇
  2004年   69篇
  2003年   69篇
  2002年   58篇
  2001年   51篇
  2000年   49篇
  1999年   53篇
  1998年   17篇
  1997年   12篇
  1996年   9篇
  1995年   10篇
  1994年   6篇
  1993年   10篇
  1992年   24篇
  1991年   25篇
  1990年   17篇
  1989年   15篇
  1988年   17篇
  1987年   21篇
  1986年   16篇
  1985年   22篇
  1984年   12篇
  1983年   13篇
  1981年   7篇
  1979年   12篇
  1978年   10篇
  1976年   13篇
  1975年   8篇
  1974年   9篇
  1973年   6篇
  1969年   6篇
  1966年   7篇
排序方式: 共有1616条查询结果,搜索用时 0 毫秒
61.
Background: The standard of care in high grade glioma (HGG) is maximal safe surgical resection followed by adjuvant radiotherapy (RT) with/without chemotherapy. For anaplastic gliomas, studies have shown use of procarbazine, lomustine, vincristine (PCV) improves overall survival (OS) and progression free survival (PFS). Currently, there is substantial evidence that molecular markers strongly predict prognosis and response to treatment. Methods: Between January 2016 to January 2018, 42 patients were accrued and followed up till April 2019. The primary end points were to correlate molecular markers with response to therapy in terms of OS and PFS in HGG. The secondary end point was to evaluate frequency of 1p/19q codeletion, IDH 1 mutation, ATRX deletion and p53 in HGG patients. Results: The median age was 46 years (range 18-67) with M:F ratio 30:12. The frequency of IDH1 mutation,1p/19q codeletion, p53 mutation and ATRX mutation were 42.8%, 16.6%, 42.8% and 14.2% respectively. All the seven patients with 1p/19q codeletion had IDH1 mutation. Median follow up was 22 months. The 20-months PFS for different mutations were as follows; IDH1-mutated vs wild type: 53.6% vs 29.8%; p-0.035, 1p/19q codeleted vs non-codeleted: 85.7% vs 62.3%; p-0.011, p53 wild type vs mutated 32.1% vs 35.6%; p-0.035 and ATRX lost vs retained: 55.6% vs 53.3%; p- 0.369. The 20-months OS for IDH1 mutated vs wild type: 82.4% vs 30.6%; p-0.014, 1p/19q codeleted vs non-codeleted: 85.7% vs 65.8%; p-0.104, p53 wild-type vs mutated 45.5% vs 73.9%; p-0.036 and ATRX lost vs retained: 100% vs 60.3%; p-0.087. Conclusion: Codeletion of 1p/19q with IDH1 mutation in HGG is associated with a significantly favourable PFS. However, larger studies with longer follow up are required to evaluate OS and PFS in all the molecular subgroups.  相似文献   
62.
In rabbits undergoing peritoneal dialysis, hypertonic (6% dextrose) dialysis solution increased the net ultrafiltration rate (UF) from 233 to 462 microL/kg/min, which was not proportional to the increment in the osmotic gradient, so the ultrafiltration coefficient decreased. As intraperitoneal dwell of hypertonic dialysate was prolonged, the gross and net UFs and ultrafiltration coefficients decreased, and the UF per dextrose absorption declined. The decrement in UF was multifactorial, including a component of fluid and solute stagnation, increasing the distance over which osmotic forces must exert their effects. Excessively hypertonic dialysis fluid should be used only briefly to achieve ultrafiltration efficiently and to avoid the high dextrose loading.  相似文献   
63.
64.
65.
Cherubism     
Cherubism, a rare tumour like lesion, is characterised by bilateral, painless, firm jaw swellings with cherubic appearance of face. It affects children of both sexes and is often familial. A case of Cherubism is being reported here because of its rarity and first from this geographical area.  相似文献   
66.
Cherubism     
Cherubism, a rare tumour like lesion, is characterised by bilateral, painless, firm jaw swellings with cherubic appearance of face. It affects children of both sexes and is often familial. A case of Cherubism is being reported here because of its rarity and first from this geographical area.  相似文献   
67.
Vocal cord dysfunction is a rare variety of upper airway obstruction characterized by typical laryngoscopic features and may mimic an acute asthma attack. The case presented in this report pertains to a 15-year-old girl who had repeated acute episodes of dyspnoea and wheezing and remained non-responsive to corticosteroids and inhaled bronchodilators requiring endotracheal intubations for adequate control. Laryngoscopic findings were consistent with vocal cord dysfunction. She was treated with a tracheostomy and psychological support.  相似文献   
68.
69.
70.
BACKGROUND: Zinc deficiency, common in developing countries, is associated with decreased immunocompetence. Zinc supplementation benefits children with acute and persistent diarrhea and prevents pneumonia. Most deaths from vaccine-preventable diseases are from measles and whooping cough; pneumonia is the most common complication of measles and often the proximate cause of related deaths. OBJECTIVE: We evaluated the effect of zinc supplementation on episodes of illness in children with measles accompanied by pneumonia. DESIGN: In a double-blind, randomized controlled trial, children aged 9 mo-15 y who were admitted to the Infectious Diseases Hospital in Calcutta with clinically severe measles accompanied by pneumonia and who had been ill for 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