全文获取类型
收费全文 | 6753篇 |
免费 | 408篇 |
国内免费 | 11篇 |
专业分类
耳鼻咽喉 | 45篇 |
儿科学 | 263篇 |
妇产科学 | 135篇 |
基础医学 | 741篇 |
口腔科学 | 107篇 |
临床医学 | 1461篇 |
内科学 | 1131篇 |
皮肤病学 | 61篇 |
神经病学 | 515篇 |
特种医学 | 119篇 |
外科学 | 561篇 |
综合类 | 76篇 |
一般理论 | 9篇 |
预防医学 | 872篇 |
眼科学 | 83篇 |
药学 | 346篇 |
中国医学 | 1篇 |
肿瘤学 | 646篇 |
出版年
2024年 | 5篇 |
2023年 | 36篇 |
2022年 | 60篇 |
2021年 | 119篇 |
2020年 | 77篇 |
2019年 | 90篇 |
2018年 | 144篇 |
2017年 | 107篇 |
2016年 | 120篇 |
2015年 | 131篇 |
2014年 | 223篇 |
2013年 | 321篇 |
2012年 | 480篇 |
2011年 | 568篇 |
2010年 | 298篇 |
2009年 | 263篇 |
2008年 | 485篇 |
2007年 | 560篇 |
2006年 | 518篇 |
2005年 | 534篇 |
2004年 | 495篇 |
2003年 | 453篇 |
2002年 | 462篇 |
2001年 | 42篇 |
2000年 | 28篇 |
1999年 | 62篇 |
1998年 | 56篇 |
1997年 | 55篇 |
1996年 | 49篇 |
1995年 | 41篇 |
1994年 | 44篇 |
1993年 | 29篇 |
1992年 | 28篇 |
1991年 | 24篇 |
1990年 | 15篇 |
1989年 | 12篇 |
1988年 | 9篇 |
1987年 | 13篇 |
1986年 | 8篇 |
1985年 | 10篇 |
1984年 | 21篇 |
1983年 | 11篇 |
1982年 | 18篇 |
1981年 | 11篇 |
1980年 | 20篇 |
1979年 | 2篇 |
1978年 | 3篇 |
1976年 | 2篇 |
1975年 | 4篇 |
1930年 | 2篇 |
排序方式: 共有7172条查询结果,搜索用时 0 毫秒
81.
82.
Ranawaka A. P. M. Perera Ronald Ko Owen T. Y. Tsang David S. C. Hui Mike Y. M. Kwan Christopher J. Brackman Esther M. W. To Hui-ling Yen Kathy Leung Samuel M. S. Cheng Kin Ho Chan Karl C. K. Chan Ka-Chi Li Linda Saif Vanessa R. Barrs Joseph T. Wu Thomas H. C. Sit Leo L. M. Poon Malik Peiris 《Journal of clinical microbiology》2021,59(2)
83.
84.
Gordana Raca Becky S Baas Salman Kirmani Jennifer J Laffin Craig A Jackson Edythe A Strand Kathy J Jakielski Lawrence D Shriberg 《European journal of human genetics : EJHG》2013,21(4):455-459
We report clinical findings that extend the phenotype of the ∼550 kb 16p11.2 microdeletion syndrome to include a rare, severe, and persistent pediatric speech sound disorder termed Childhood Apraxia of Speech (CAS). CAS is the speech disorder identified in a multigenerational pedigree (‘KE'') in which half of the members have a mutation in FOXP2 that co-segregates with CAS, oromotor apraxia, and low scores on a nonword repetition task. Each of the two patients in the current report completed a 2-h assessment protocol that provided information on their cognitive, language, speech, oral mechanism, motor, and developmental histories and performance. Their histories and standard scores on perceptual and acoustic speech tasks met clinical and research criteria for CAS. Array comparative genomic hybridization analyses identified deletions at chromosome 16p11.2 in each patient. These are the first reported cases with well-characterized CAS in the 16p11.2 syndrome literature and the first report of this microdeletion in CAS genetics research. We discuss implications of findings for issues in both literatures. 相似文献
85.
86.
87.
Lukas F. Mager Carsten Riether Christian M. Schürch Yara Banz Marie-Hélène Wasmer Regula Stuber Alexandre P. Theocharides Xiaohong Li Yu Xia Hirohisa Saito Susumu Nakae Gabriela M. Baerlocher Markus G. Manz Kathy D. McCoy Andrew J. Macpherson Adrian F. Ochsenbein Bruce Beutler Philippe Krebs 《The Journal of clinical investigation》2015,125(7):2579-2591
Myeloproliferative neoplasms (MPNs) are characterized by the clonal expansion of one or more myeloid cell lineage. In most cases, proliferation of the malignant clone is ascribed to defined genetic alterations. MPNs are also associated with aberrant expression and activity of multiple cytokines; however, the mechanisms by which these cytokines contribute to disease pathogenesis are poorly understood. Here, we reveal a non-redundant role for steady-state IL-33 in supporting dysregulated myelopoiesis in a murine model of MPN. Genetic ablation of the IL-33 signaling pathway was sufficient and necessary to restore normal hematopoiesis and abrogate MPN-like disease in animals lacking the inositol phosphatase SHIP. Stromal cell–derived IL-33 stimulated the secretion of cytokines and growth factors by myeloid and non-hematopoietic cells of the BM, resulting in myeloproliferation in SHIP-deficient animals. Additionally, in the transgenic JAK2V617F model, the onset of MPN was delayed in animals lacking IL-33 in radio-resistant cells. In human BM, we detected increased numbers of IL-33–expressing cells, specifically in biopsies from MPN patients. Exogenous IL-33 promoted cytokine production and colony formation by primary CD34+ MPN stem/progenitor cells from patients. Moreover, IL-33 improved the survival of JAK2V617F-positive cell lines. Together, these data indicate a central role for IL-33 signaling in the pathogenesis of MPNs. 相似文献
88.
Miriam Hwang Kathy Zebracki Lawrence C. Vogel 《Topics in spinal cord injury rehabilitation》2015,21(1):10-19
Background:
Employment rates among individuals with spinal cord injury (SCI) are lower than in the general population and little is known about the specific occupations in which they are employed.Objectives:
To describe specific occupations of adults with pediatric-onset SCI using the 2010 Standard Occupational Classification (SOC) system and to determine associations between SOC occupations and demographic factors.Methods:
Cross-sectional data specific to education and employment were collected from the last interviews of a larger longitudinal study. Occupations were categorized according to the 2010 SOC system. SOC groups were compared within gender level of injury and final education.Results:
Of the 461 total participants 219 (47.5%) were employed and specific occupations were available for 179. Among the SOC groups Education Law Community Service Arts and Media Occupations were most prevalent (30.2%) followed by Management Business and Finance Occupations (21.1%) Computer Engineering and Science Occupations (10.6%) Administrative and Office Support Occupations (10.0%) Service Occupations (7.3%) Healthcare Practitioners and Technical Occupations (3.9%) and Production Occupations (3.4%). Differences were found in the distribution of SOC groups between gender levels of injury and final education groups.Conclusion:
A wide variety of occupations were reported in adults with pediatric-onset SCI generally in concordance with final education and functional ability levels. 相似文献89.
90.