全文获取类型
收费全文 | 6053篇 |
免费 | 512篇 |
国内免费 | 2篇 |
出版年
2023年 | 38篇 |
2022年 | 20篇 |
2021年 | 69篇 |
2020年 | 73篇 |
2019年 | 83篇 |
2018年 | 138篇 |
2017年 | 109篇 |
2016年 | 182篇 |
2015年 | 213篇 |
2014年 | 260篇 |
2013年 | 375篇 |
2012年 | 503篇 |
2011年 | 455篇 |
2010年 | 239篇 |
2009年 | 264篇 |
2008年 | 385篇 |
2007年 | 357篇 |
2006年 | 307篇 |
2005年 | 312篇 |
2004年 | 289篇 |
2003年 | 234篇 |
2002年 | 218篇 |
2001年 | 172篇 |
2000年 | 123篇 |
1999年 | 130篇 |
1998年 | 56篇 |
1997年 | 38篇 |
1996年 | 39篇 |
1995年 | 34篇 |
1994年 | 39篇 |
1993年 | 29篇 |
1992年 | 65篇 |
1991年 | 45篇 |
1990年 | 53篇 |
1989年 | 42篇 |
1988年 | 52篇 |
1987年 | 40篇 |
1986年 | 53篇 |
1985年 | 43篇 |
1984年 | 24篇 |
1983年 | 22篇 |
1982年 | 22篇 |
1981年 | 22篇 |
1980年 | 17篇 |
1979年 | 35篇 |
1978年 | 27篇 |
1977年 | 20篇 |
1976年 | 17篇 |
1975年 | 22篇 |
1974年 | 30篇 |
排序方式: 共有6567条查询结果,搜索用时 15 毫秒
1.
2.
Thomas?Durand Sophie?Jacob Laura?Lebouil Hassen?Douzane Philippe?Lestaevel Amithys?Rahimian Dimitri?Psimaras Lo?c?Feuvret Delphine?Leclercq Bruno?Brochet Radia?Tamarat Fabien?Milliat Marc?Benderitter Nicolas?Vayatis Georges?No?l Khê?Hoang-Xuan Jean-Yves?Delattre Damien?Ricard Marie-Odile?BernierEmail author 《BMC neurology》2015,15(1):261
Background
Radiotherapy is one of the most important treatments of primary and metastatic brain tumors. Unfortunately, it can involve moderate to severe complications among which leukoencephalopathy is very frequent and implies cognitive deficits such as memory, attention and executive dysfunctions. However, the incidence of this complication is not well established and the risk factors and process are poorly understood. The main objective of the study is to improve knowledge on radio-induced leukoencephalopathy based on pluridisciplinar approaches combining cognitive, biologic, imagery and dosimetric investigations.Method/Design
The EpiBrainRad study is a prospective cohort study including newly diagnosed high grade gliomas patients treated by radiotherapy and concomitant-adjuvant temozolomide chemotherapy. Patients are included between their surgery and first day of radio-chemotherapy, and the follow-up lasts for 3 years after treatment. Cognitive functioning assessments, specific blood biomarkers measures and magnetic resonance imagery are performed at different moment during the follow-up, and a specific dosimetric assessment of organs involved in the beam fields is performed. Firstly, leukoencephalopathy incidence rate will be estimated in this population. Secondly, correlations between cognitive impairments and dosimetry, biomarkers ranges and anomalies on imagery will be analyzed in order to better understand the onset and evolution of cognitive decrement associated with radiotherapy. Furthermore, a new cognitive test, quickly and easily performed, will be studied to determine its sensibility to detect leukoencephalopathy decrement.Discussion
With an original multidisciplinary approach, the EpiBrainRad study aims to improve knowledge on radio-induced leukoencephalopathy in order to improve its early diagnosis and prevention. The main challenge is to preserve quality-of-life after cancer treatments which imply to study the incidence of radiation-induced complications and their associated risk factors.Trial Registration
NCT025441783.
S T Chen L C Lo S H Wu K T Wang 《International journal of peptide and protein research》1990,35(1):52-54
2-Oxazolidone derivatives formed through an intramolecular reaction in the process of alkaline treatment of urethane-type N-protected peptides of which the N-terminal residues were Ser or Thr having unprotected hydroxyl groups. In oder to avoid this side reaction, the esters of these peptides could be cleaved by enzymatic hydrolyses instead of saponification. 相似文献
4.
5.
Stefano Bastianini Alessandro Silvani Chiara Berteotti Viviana Lo Martire Gary Cohen Hiroshi Ohtsu Jian-Sheng Lin Giovanna Zoccoli 《PloS one》2015,10(10)
Narcolepsy type 1 is associated with loss of orexin neurons, sleep-wake derangements, cataplexy, and a wide spectrum of alterations in other physiological functions, including energy balance, cardiovascular, and respiratory control. It is unclear which narcolepsy signs are directly related to the lack of orexin neurons or are instead modulated by dysfunction of other neurotransmitter systems physiologically controlled by orexin neurons, such as the histamine system. To address this question, we tested whether some of narcolepsy signs would be detected in mice lacking histamine signaling (HDC-KO). Moreover, we studied double-mutant mice lacking both histamine signaling and orexin neurons (DM) to evaluate whether the absence of histamine signaling would modulate narcolepsy symptoms produced by orexin deficiency. Mice were instrumented with electrodes for recording the electroencephalogram and electromyogram and a telemetric arterial pressure transducer. Sleep attacks fragmenting wakefulness, cataplexy, excess rapid-eye-movement sleep (R) during the activity period, and enhanced increase of arterial pressure during R, which are hallmarks of narcolepsy in mice, did not occur in HDC-KO, whereas they were observed in DM mice. Thus, these narcolepsy signs are neither caused nor abrogated by the absence of histamine. Conversely, the lack of histamine produced obesity in HDC-KO and to a greater extent also in DM. Moreover, the regularity of breath duration during R was significantly increased in either HDC-KO or DM relative to that in congenic wild-type mice. Defects of histamine transmission may thus modulate the metabolic and respiratory phenotype of murine narcolepsy. 相似文献
6.
James C. Lo Sanda Ljubicic Barbara Leibiger Matthias Kern Ingo B. Leibiger Tilo Moede Molly E. Kelly Diti Chatterjee Bhowmick Incoronata Murano Paul Cohen Alexander S. Banks Melin J. Khandekar Arne Dietrich Jeffrey S. Flier Saverio Cinti Matthias Blüher Nika N. Danial Per-Olof Berggren Bruce M. Spiegelman 《Cell》2014
7.
L. Lacoste‐Collin D. d'Aure E. Bérard I. Rouquette M. B. Delisle M. Courtade‐Saïdi 《Cytopathology》2014,25(3):160-169
8.
9.
Four coumaronochromones, formosanatins A–D (Fig. 1 and Fig. 2–4), and a flavanone, euchrenone a16 (Fig. 1 and Fig. 2), along with four known compounds, euchretins E and G, euchrestaflavanone A, and daidzein, were isolated from the roots of Euchresta formosana. The structures of Fig. 1 and Fig. 2– Fig. 1 and Fig. 2 were established by spectroscopic analyses. 相似文献
10.
E Sbidian S Hadj-Rabia VM Riccardi L Valeyrie-Allanore S Barbarot O Chosidow S Ferkal D Rodriguez P Wolkenstein S Bastuji-Garin 《Orphanet journal of rare diseases》2012,7(1):62
ABSTRACT: OBJECTIVE: To identify clinical characteristics associated with internal neurofibromas in children with NF1, as a means of ensuring the early identification of patients at high risk for malignant peripheral nerve-sheath tumors developed from preexisting internal neurofibromas.Patients and methodsWe used data from two NF1 populations, in France and North America, respectively. The French database comprised 1083 patients meeting NIH diagnostic criteria for NF1 and the Neurofibromatosis Institute Database of North America comprised 703 patients. Patients younger than 17 years of age were eligible for our study if they had been evaluated for internal neurofibromas using computed tomography and/or magnetic resonance imaging. Clinical characteristics associated with internal neurofibromas by univariate analysis (P [LESS-THAN OR EQUAL TO] 0.15) were entered into a multiple logistic regression model after checking for potential interactions and confounding. Multiple imputation was used for missing values. RESULTS: Among the 746 children in the two databases, 357 (48%) met our inclusion criteria. Their mean age was 7.7 [PLUS-MINUS SIGN] 5.0 years and there were 192 (53.8%) males. Internal neurofibromas were present in 35 (9.8%) patients. Internal neurofibromas developed earlier in females than in males and their prevalence increased during adolescence. Factors independently associated with internal neurofibromas were age (OR = 1.16 [1.07-1.27]), xanthogranulomas (OR = 5.85 [2.18-15.89]) and presence of both subcutaneous and plexiform neurofibromas (OR = 6.80 [1.52-30.44]). CONCLUSIONS: Several easily recognizable clinical characteristics indicate a high risk of internal neurofibromas in children with NF1 and, therefore, a need for very close monitoring. 相似文献