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   6294篇
  免费   1篇
电工技术   5篇
综合类   1篇
化学工业   22篇
建筑科学   1篇
轻工业   1篇
石油天然气   1篇
无线电   5篇
一般工业技术   6篇
冶金工业   6249篇
自动化技术   4篇
  2019年   1篇
  2015年   2篇
  2013年   2篇
  2010年   1篇
  2009年   2篇
  2008年   1篇
  2007年   1篇
  2005年   2篇
  2004年   6篇
  2003年   18篇
  2002年   3篇
  2001年   1篇
  2000年   1篇
  1999年   203篇
  1998年   1984篇
  1997年   1082篇
  1996年   777篇
  1995年   401篇
  1994年   333篇
  1993年   365篇
  1992年   42篇
  1991年   87篇
  1990年   49篇
  1989年   68篇
  1988年   64篇
  1987年   65篇
  1986年   67篇
  1985年   48篇
  1983年   6篇
  1982年   24篇
  1981年   38篇
  1980年   62篇
  1979年   6篇
  1978年   16篇
  1977年   135篇
  1976年   314篇
  1975年   11篇
  1973年   1篇
  1955年   5篇
  1954年   1篇
排序方式: 共有6295条查询结果,搜索用时 15 毫秒
81.
82.
83.
84.
85.
Geleophysic dysplasia is a rare, autosomal recessive disorder which causes disproportionate short stature associated with severe physical handicaps, but is compatible with survival into adulthood. We present a case, a first-born child, where genetic counselling difficulties arose following ultrasound recognition of short-limbed dwarfism in association with polyhydramnios and an initial incorrect prenatal diagnosis of lethal chondrodysplasia. After birth of the surviving affected infant, the parents had great difficulty accepting that there had been a prenatal misdiagnosis and they were greatly disappointed by our inability to predict the postnatal survival of an infant to whom no hope of life had previously been given. The correct diagnosis was not made until the proband was nearly 1 year old, and the true prognosis then became clearer. This experience underlines the relative ease of prenatal recognition of skeletal growth abnormalities compared with the considerable difficulties experienced in reaching a precise diagnosis. Thus, following prenatal diagnosis of unspecified chondrodysplasia when parents seek definite information about the prognosis, the temptation to be either overpessimistic or overoptimistic should be avoided.  相似文献   
86.
A direct waveform mean-shape vector quantization (MSVQ) is proposed here as an alternative for electrocardiographic (ECG) signal compression. In this method, the mean values for short ECG signal segments are quantized as scalars and compression of the single-lead ECG by average beat substraction and residual differencing their waveshapes coded through a vector quantizer. An entropy encoder is applied to both, mean and vector codes, to further increase compression without degrading the quality of the reconstructed signals. In this paper, the fundamentals of MSVQ are discussed, along with various parameters specifications such as duration of signal segments, the wordlength of the mean-value quantization and the size of the vector codebook. The method is assessed through percent-residual-difference measures on reconstructed signals, whereas its computational complexity is analyzed considering its real-time implementation. As a result, MSVQ has been found to be an efficient compression method, leading to high compression ratios (CR's) while maintaining a low level of waveform distortion and, consequently, preserving the main clinically interesting features of the ECG signals. CR's in excess of 39 have been achieved, yielding low data rates of about 140 bps. This compression factor makes this technique especially attractive in the area of ambulatory monitoring.  相似文献   
87.
The aim of work was evaluation of voice pathology in patients with allergic rhinitis. Larynx organic pathology were found in 75% patients with coexisting allergic rhinitis in the form of Reinke's oedema, chronic hypertrophic laryngitis, larynx polyp and vocal nodules. It caused serious voice pathology (dysphonia) which was confirmed by an objective spectrographic method. Larynx organic pathology was not in 15% patients. In these cases rhinophonia was found in consequence of resonance nasal defect.  相似文献   
88.
Knowledge of human leucocyte antigen (HLA) peptide binding motifs permits rapid selection of candidate viral protein fragments for induction of T cell-mediated immunity. A search for HLA class I peptide binding motifs in structural proteins of human immunodeficiency virus (HIV) of different genetic lineages provides a map of the genetic organization of potential T cell antigenic sites, and at the same time identifies all motifs in highly conserved regions of HIV-1 env, gag and pol. The density of motifs is anomalous at both the high and low end of the spectrum: local organization is characterized by clustering in relatively short regions, while large scale organization is characterized by anomalously long runs between motifs. The former is expected simply due to the fact that motifs often have overlapping anchor residue sets. A detailed statistical analysis of the latter, however, shows that the length of the runs cannot be accounted for by chance alone. Although motif clusters show no preference to be in either conserved or variable regions, low motif density stretches occur preferentially in variable portions of the protein sequence, which suggests that the virus may be mutating to evade the cellular arm of the immune system.  相似文献   
89.
90.
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