全文获取类型
收费全文 | 46篇 |
免费 | 0篇 |
专业分类
化学 | 20篇 |
数学 | 2篇 |
物理学 | 24篇 |
出版年
2011年 | 1篇 |
2008年 | 1篇 |
2006年 | 1篇 |
2003年 | 1篇 |
2002年 | 2篇 |
2001年 | 1篇 |
2000年 | 2篇 |
1998年 | 2篇 |
1996年 | 2篇 |
1995年 | 3篇 |
1993年 | 1篇 |
1991年 | 1篇 |
1988年 | 1篇 |
1984年 | 1篇 |
1982年 | 1篇 |
1981年 | 5篇 |
1979年 | 2篇 |
1974年 | 1篇 |
1972年 | 1篇 |
1934年 | 1篇 |
1932年 | 1篇 |
1931年 | 1篇 |
1930年 | 1篇 |
1924年 | 1篇 |
1923年 | 2篇 |
1919年 | 2篇 |
1917年 | 1篇 |
1912年 | 1篇 |
1909年 | 1篇 |
1907年 | 1篇 |
1904年 | 3篇 |
排序方式: 共有46条查询结果,搜索用时 15 毫秒
1.
2.
3.
An intraindividual study of the characteristics of erythema induced by bath and oral methoxsalen photochemotherapy and narrowband ultraviolet B 总被引:1,自引:0,他引:1
We compared the characteristics of psoralen and ultraviolet A (PUVA) erythema in skin photosensitized by bath or oral methoxsalen in 20 subjects. Erythema was assessed visually and with a reflectance instrument at 24 h intervals for 7 days. In addition, narrowband ultraviolet B (TL-01 UVB) erythema was examined in 19 of these subjects at 4, 8, 12, 24, 48 and 72 h and in another nine subjects at 12, 15, 18, 21 and 24 h. Both bath and oral PUVA exhibited broad erythemal peaks beyond 72 h. For topical PUVA the lowest minimal phototoxic dose (MPD) occurred at 120 and 144 h (P = 0.01 and 0.03 compared with 72 h). Oral PUVA erythema peaked earlier at 96 h: the MPD was significantly lower at 96, 120 and 144 h compared with 72 h (P = 0.001, 0.01 and 0.02, respectively). At 120 h, bath PUVA had a significantly steeper slope compared with oral PUVA. The TL-01 UVB minimal erythema dose was significantly lower at 12 h compared with 24 h (P = 0.019). The majority of subjects were at maximal erythema at 12 h (22 of 28) and 15 h (eight of nine). Our results suggest that peak erythema for bath PUVA, oral PUVA and TL-01 UVB occurs at 120, 96 and 12-15 h, respectively. 相似文献
4.
5.
Navin A Anthony DW Aumann T Baumann T Bazin D Blumenfeld Y Brown BA Glasmacher T Hansen PG Ibbotson RW Lofy PA Maddalena V Miller K Nakamura T Pritychenko BV Sherrill BM Spears E Steiner M Tostevin JA Yurkon J Wagner A 《Physical review letters》2000,84(2):266-269
We derive the formalism to obtain spatial distributions of collisional correlation times for macroscopic particles undergoing granular flow from pulsed gradient spin echo nuclear magnetic resonance diffusion data. This is demonstrated with an example of axial motion in the shear flow regime of a 3D granular flow in a horizontal rotating cylinder at one rotation rate. 相似文献
6.
E. R. E. Müller H. Phillips Chemikerausschuss des U. S. Stahlverbandes Haripada Bhattacharyya L. T. Bowser Fr. Ibbotson H. Brearley R. J. Wysor F. W. Hinrichsen Th. Dieckmann G. Misson R. Schröder D. Chouchak Ph. A. Kober und Grete Egerer 《Fresenius' Journal of Analytical Chemistry》1917,56(8):396-405
Ohne Zusammenfassung 相似文献
7.
N. Howell Furman W. Le Roy Mc Cay A. Kling A. Lassieur F. Ibbotson L. Aitchison C. S. Marvel und O. Kamm 《Fresenius' Journal of Analytical Chemistry》1924,65(3-4):153-155
Ohne Zusammenfassung 相似文献
8.
9.
10.
Valentine RM Ibbotson SH Brown CT Wood K Moseley H 《Photochemistry and photobiology》2011,87(1):242-249
The characteristics of protoporphyrin IX (PPIX) fluorescence in superficial basal cell carcinoma (sBCC) and carcinoma in situ (Bowen's Disease, BD) following application of 5-aminolaevulinic acid (5-ALA) and its methyl ester (methyl aminolevulinate [MAL]) before, during and after photodynamic therapy (PDT) were investigated in 40 patients. Photosensitizer prodrug penetration can limit PDT efficacy and understanding the characteristics of PPIX fluorescence through fluorescence spectroscopy, may improve knowledge of photosensitizer delivery. Fluorescence intensity was assessed quantitatively, and the rate of photobleaching was determined by fitting an exponential decay. As a secondary end-point, PDT-induced pain was also measured continuously during treatment using a novel hand-held device, known as a pain logger. In vivo PPIX fluorescence was shown to decrease during irradiation, allowing the in vivo photobleaching of PPIX to be monitored. No significant difference was found between ALA- or MAL-induced PPIX fluorescence in lesions of sBCC and BD (P>0.05), indicating no detectable difference in PPIX kinetics for the two prodrugs as assessed by these measures. Pain, as assessed by the logger device, showed high interindividual variability and pain levels tended to be higher initially, decreasing during treatment. No difference was seen in pain experienced during ALA-or MAL-PDT (P>0.05). 相似文献