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		题名	作者	年代	出处	被引量
	1	Method for size optimisation of large wind–hydrogen systems with high penetration on power grids显示文摘	M. Beccali S. Brunone P. Finocchiaro J.M. Galletto	2013	Applied Energy2013，，：	1
	2	Silicon Geiger mode avalanche photodiodes显示文摘In this letter we present the results regarding the electrical and optical characterization of Geiger mode silicon avalanche photodiodes(GMAP) fabricated by silicon standard planar technology. Low dark count rates,negligible afterpulsing effects,good timing resolution and high quantum detection efficiency in all the visible range have been measured. The very good electro-optical performances of our photodiodes make them attractive for the fabrication of arrays with a large number of GMAP to be used both in the commercial and the scientific fields,as telecommunications and nuclear medical imaging.	M. Mazzillo G. Condorelli D. Sanfilippo G. Fallica E. Sciacca S. Aurite S. Lombardo E. Rimini M. Belluso S. Billotta G. Bonanno A. Campisi L. Cosentino P. Finocchiaro F. Musumeci S. Privitera S. Tudisco	2007	Optoelectronics Letters2007，3，3：	1
	3	在囊性纤维化患儿中中性粒细胞谷氨酰胺缺乏与基因型的关系显示文摘Pulmonary disease in cystic fibrosis (CF) is characterized by a chronic neutrophil-dominated inflammation of lung tissue. Inasmuch as some amino acids (AA) play a pivotal role in various aspects of neutrophil metabolism,the aim of this study was to investigate a possible alteration of neutrophil AA metabolism and to evaluate its relation (if any) with the genotype. We performed plasma and neutrophil AA analysis in 26 CF patients with known genotype,10 patients with non-CF bronchiectasis,and 20 normal subjects. The CF group showed a significant decrease of free intracellular neutrophil glutamine (Gln) content compared with controls and the non-CF bronchiectasis group. In the latter group,levels of neutrophil Gln were significantly lower compared with the controls. Amino acid plasma concentration in non-CF bronchiectasis showed a decrease of Gln and taurine compared with controls. Neutrophil Gln content showed values significantly lower in CF patients with severe mutations (class I,II,and III mutations) compared with mild mutations (class IV and V mutations). Results of our study add further evidence for intrinsic neutrophil alterations that could play an important role in the pathogenesis of chronic pulmonary disease in CF patients.	D'Eufemia P. Finocchiaro R. Celli M. 刘凯	2006	世界核心医学期刊文摘(儿科学分册)2006，0，12：	0

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