Titlebook: ;

children

書目名稱影響因子(影響力)




書目名稱影響因子(影響力)學(xué)科排名




書目名稱網(wǎng)絡(luò)公開度




書目名稱網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱被引頻次




書目名稱被引頻次學(xué)科排名




書目名稱年度引用




書目名稱年度引用學(xué)科排名




書目名稱讀者反饋




書目名稱讀者反饋學(xué)科排名

debunk

不感興趣

arrhythmic

ALIBI

Prinzipien der diskreten und integralen Signaltransformation,en genannt, und Integraltransformationen. Bei diskreten Transformationen werden die Signale durch diskrete Werte (N-Tupel) repr?sentiert. Die Signale selbst k?nnen durchaus zeitkontinuierlich sein. Bei einer Integraltransformation wird das Signal durch eine Dichtefunktion bezüglich eines Transformationskerns beschrieben.

Libido

R. Marinospecialized literature, we have found very little work about MAS methodologies that allow us to build MAS which is made up of two or more MASs. We think that several difficult challenges for automated systems can be tackled by giving full meaning to the MAS concept: adopting a recursive definition o

–吃

Karen Englanderare co-engineering. Different from the traditional software engineering process, it is a mixed process involving both software engineering and knowware engineering issues. The technical subtleties of such a mixed process are discussed and guidelines of building models for it are proposed. It involve

Coronary

Nonlinear Devices, sources. In 1961, .. [10.1] and coworkers detected ultraviolet light at twice the frequency of a ruby laser beam when this beam was propagated through a quartz crystal. This experiment marked the beginning of an intense investigation into the realm of the nonlinear optical properties of matter.

Expertise

https://doi.org/10.1007/978-3-642-15289-4for assessing the activity of several lysosomal enzymes in . (α-galactosidase, β-galactosidase, α-glucosidase, β-glucosidase, β-N-acetylglucosaminidase, α-mannosidase, cathepsin B, cathepsin D, cathepsin F, palmitoyl protein thioesterase 1, and tripeptidyl peptidase 1).

foodstuff

Clinical Aspects of Genetic Forms of Nephrotic Syndromeas ciliary or tubular genes and has widened the phenotypes associated with SRNS. More complex inheritance involving susceptibility variants, oligogenism or interallelic influence of variants have also been described as a cause of SRNS.