全文获取类型
收费全文 | 362篇 |
免费 | 26篇 |
国内免费 | 1篇 |
专业分类
儿科学 | 11篇 |
妇产科学 | 7篇 |
基础医学 | 51篇 |
口腔科学 | 1篇 |
临床医学 | 24篇 |
内科学 | 76篇 |
皮肤病学 | 17篇 |
神经病学 | 44篇 |
特种医学 | 34篇 |
外科学 | 28篇 |
综合类 | 3篇 |
预防医学 | 60篇 |
眼科学 | 7篇 |
药学 | 12篇 |
中国医学 | 1篇 |
肿瘤学 | 13篇 |
出版年
2023年 | 6篇 |
2022年 | 32篇 |
2021年 | 38篇 |
2020年 | 11篇 |
2019年 | 20篇 |
2018年 | 22篇 |
2017年 | 15篇 |
2016年 | 16篇 |
2015年 | 16篇 |
2014年 | 15篇 |
2013年 | 21篇 |
2012年 | 29篇 |
2011年 | 38篇 |
2010年 | 18篇 |
2009年 | 14篇 |
2008年 | 17篇 |
2007年 | 11篇 |
2006年 | 17篇 |
2005年 | 13篇 |
2004年 | 8篇 |
2003年 | 4篇 |
2002年 | 5篇 |
2001年 | 1篇 |
1998年 | 2篇 |
排序方式: 共有389条查询结果,搜索用时 15 毫秒
361.
Khaoula Ben-Farhat Imen Ben-Mustapha Meriem Ben-Ali Karen Rouault Saber Hamami Najla Mekki Amel Ben-chehida Beya Larguèche Zohra Fitouri Selim Abdelmoula Monia khemiri Mohamed-Neji Guediche Samir Boukthir Sihem Barsaoui Jalel Chemli Mohamed-Ridha Barbouche 《Journal of clinical immunology》2016,36(6):547-554
Chronic granulomatous disease (CGD) is the prototypic functional neutrophil disorder caused by genetic defects in one of the five genes encoding the superoxide-generating nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase subunits of phagocytes. Mutations causing the most prevalent form of CGD in western populations are located in the X-linked-CYBB gene. The four remaining autosomal recessive (AR) forms collectively account for one-third of CGD cases. We investigated the clinical and molecular features of eleven patients with CGD from 6 consanguineous families, originating from contiguous regions in the west of Tunisia. The patients’ clinical phenotype is characterized by a high incidence of mycobacterial infections. Five out of the eleven patients died despite treatment arguing in favor of a severe clinical form of CGD. These findings correlated with the absence of functional p67phox protein as well as the absence of residual reactive oxygen intermediates (ROI) production. Genetic analysis showed the presence, in all patients, of a unique mutation (c.257 + 2T > C) in NCF2 gene predicted to affect RNA splicing. Segregating analysis using nine polymorphic markers overlapping the NCF2 gene revealed a common haplotype spanning 4.1 Mb. The founder event responsible for this mutation was estimated to have arisen approximately 175 years ago. These findings will facilitate the implementation of preventive approaches through genetic counseling in affected consanguineous families. 相似文献
362.
Amal Akammar Sylvie Kolani Zineb Benchekroune Nizar EL Bouardi Meriem Haloua Moulay Youssef Alaoui Lamrani Meryem Boubbou Mounia Serraj Mohamed Smahi Maaroufi Maroufi Badreeddine Alami 《Radiology Case Reports》2021,16(9):2570
Thymolipoma is a rare benign neoplasm of the thymus containing both mature adipose tissue and thymic tissue. We report a case of a 34‐year‐οld man, presenting a mass of the anterior mediastinum, the radiology investigation and operatory piece diagnosed a thymolipoma.This study highlights the clinical diagnostic and therapeutic features as well as the evolutionary characteristics of this entity. 相似文献
363.
Negar Babae Meriem Bourajjaj Yijia Liu Judy R. Van Beijnum Francesco Cerisoli Puthupparampil V. Scaria Mark Verheul Maaike P. Van Berkel Ebel H. E. Pieters Rick J. Van Haastert Afrouz Yousefi Enrico Mastrobattista Gert Storm Eugene Berezikov Edwin Cuppen Martin Woodle Roel Q. J. Schaapveld Gregoire P. Prevost Arjan W. Griffioen Paula I. Van Noort Raymond M. Schiffelers 《Oncotarget》2014,5(16):6687-6700
364.
365.
366.
The tumor microenvironment is a complex system playing an important role in tumor development and progression. Besides tumor cells, the tumor microenvironment harbours a variety of host-derived cells, such as endothelial cells, fibroblasts, innate and adaptive immune cells, as well as extracellular matrix (ECM) fibers, cytokines, and other mediators. This review discusses the potential role of hypoxia and endothelial cells within tumor microenvironment and emphasizes their interaction with antigen specific killer cells. 相似文献
367.
368.
369.
370.