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As providers of frontline clinical care for patients with acute and potentially life-threatening infections, emergency departments (EDs) have the priorities of saving lives and providing care quickly and efficiently. Although these facilities see a diversity of patients 24 hours per day and can collect prospective data in real time, their ability to conduct timely research on infectious syndromes is not well recognized. ncy ID NET is a national network that demonstrates that EDs can also collect data and conduct research in real time. This network collaborates with the Centers for Disease Control and Prevention (CDC) and other partners to study and address a wide range of infectious diseases and clinical syndromes. In this paper, we review selected highlights of ncy ID NET's history from 1995 to 2017. We focus on the establishment of this multisite research network and the network's collaborative research on a wide range of ED clinical topics.
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http://dx.doi.org/10.1093/ofid/ofx218 | DOI Listing |
Foods
September 2022
Dipartimento Scienze Della Vita e Dell'Ambiente, Università Politecnica Delle Marche, Via Brecce Bianche, 60131 Ancona, Italy.
During the last few years, consumer demand has been increasingly oriented to fermented foods with functional properties. This work proposed to use selected non-conventional yeasts (NCY) and in pure and mixed fermentation to produce craft beer fortified with hydrolyzed red lentils (HRL). For this, fermentation trials using pils wort (PW) and pils wort added with HRL (PWL) were carried out.
View Article and Find Full Text PDFJ Mol Graph Model
March 2016
Laboratory of Theoretical Chemistry, Department of Chemistry, University of Maragheh, P.O. Box 5513864596, Maragheh, Iran.
The geometries, interaction energies and bonding properties of cationic pnicogen bond (CPB) interactions are studied in binary XH3P(+)⋯NCY (X=H, F, CN, NH2, OH; Y=H, Li, F, Cl) complexes by means of MP2/aug-cc-pVTZ calculations. Interaction energies of these binary complexes span a large range, from -16.36kcal/mol in (NH2)H3P(+)⋯NCF to -71.
View Article and Find Full Text PDFDalton Trans
September 2012
Fakultät für Chemie der Universität Bielefeld, 33615 Bielefeld, Germany.
Two linear π-conjugated systems with 1,3-diethyl-1,3,2-benzodiazaborolyl [C(6)H(4)(NEt)(2)B-] as a donor group and dimesitylboryl (-BMes(2)) as acceptor were synthesised with -ethynylene-phenylene- (-C≡C-1,4-C(6)H(4)-, 3) and -ethynylene-thiophene- (-C≡C-2,5-C(4)H(2)S-12) bridges between the boron atoms. An assembly (20) consisting of two diazaborolyl-ethynylene-phenylene-boryl units, [C(6)H(4)(NCy)(N')B-C≡C-1,4-C(6)H(4)-BMes(2)] joined via a 1,4-phenylene unit at the nitrogen atoms (N') of the diazaborolyl units was also synthesised. The three push-pull systems, 3, 12 and 20, form salts on fluoride addition with the BMes(2) groups converted into (BMes(2)F)(-) anions.
View Article and Find Full Text PDFDalton Trans
August 2010
School of Chemistry, University of Nottingham, University Park, Nottingham, UK NG7 2RD.
Reaction of three equivalents of ArNH(2) (Ar = 3,5-Me(2)C(6)H(3)) with HC(SiMe(2)Br)(3) in the presence of the auxiliary base NEt(3) afforded the tripodal tris(N-arylamine-dimethylsilyl)methane HC{SiMe(2)N(H)Ar}(3) (1) in 83% yield. Three-fold deprotonation of 1 with n-butyllithium afforded the corresponding tri-lithium tris(N-arylamido-dimethylsilyl)methane etherate [HC{SiMe(2)N(Li)Ar}(3)(OEt(2))] (2) in 92% yield. Salt elimination reactions between 2 or the known complex [HC{SiMe(2)N(Li)Ar'}(3)(OEt(2))(2)] (3) (Ar' = 4-MeC(6)H(4)) with one equivalent of uranium(IV) tetrachloride afforded the corresponding tris(N-arylamido-dimethylsilyl)methane uranium(IV) chloride complexes as monomeric [U(Cl){HC(SiMe(2)NAr)(3)}(THF)] (4) and dinuclear [{HC(SiMe(2)NAr')(3)}U(Cl)(mu-Cl)U(THF)(2){(Ar'NSiMe(2))(3)CH}] (5) species in 70 and 90% crystalline yields, respectively.
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August 2010
Department of Chemistry, University of Bari, Campus Universitario, Bari and CIRCC, via Celso Ulpiani 27, Bari, Italy.
NbCl(5) x (N,N'-dicyclohexylurea) 1a owns a distorted octahedral structure due to intramolecular NH...
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