Chiral Dynamics and Fermion Mass Generation in Three Dimensional Gauge Theory

Autor: Sodano, M. C. Diamantini G. W. Semenoff P.

Publikováno v: Phys.Rev.Lett. 70 (1993) 3848-3851

We examine the possibility of fermion mass generation in 2+1- dimensional gauge theory from the current algebra point of view.In our approach the critical behavior is governed by the fluctuations of pions which are the Goldstone bosons for chiral sym

Externí odkaz: http://arxiv.org/abs/hep-ph/9301256

Post-operative ileus in hemicolectomy for cancer: open versus laparoscopic approach

Autor: Procacciante F, De Luca M, Abilaliaj V, Massimo Chiaretti, Diamantini G

Publikováno v: Scopus-Elsevier
Massimo Chiaretti
Europe PubMed Central

This study aims to verify if the duration of postoperative ileus (POI), in patients undergoing abdominal surgery, is related to the surgical approach used (open or laparoscopic) or rather to the manipulation of bowel loops.Ninety patients, undergoing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::045bd8c41ac4720156a76cc60e510840
https://pubmed.ncbi.nlm.nih.gov/24140940

Complicanze maggiori nelle colectomie per cancro: confronto fra tecnica open vs laparoscopia

Autor: Procacciante, Fabio, Diamantini, G, Caciolo, F.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3686::7de44ac5026f0ba2d84706181199c739
http://hdl.handle.net/11573/189233

Reassessing the melatonin pharmacophore--enantiomeric resolution, pharmacological activity, structure analysis, and molecular modeling of a constrained chiral melatonin analogue

Autor: Rivara S., Diamantini G., Di Giacomo B., Lamba D., Gatti G., Lucini V., Pannacci M., Mor M., Spadoni G., Tarzia G.

Publikováno v: Bioorganic & medicinal chemistry
14 (2006): 3383–3391.
info:cnr-pdr/source/autori:Rivara S., Diamantini G., Di Giacomo B., Lamba D., Gatti G., Lucini V., Pannacci M., Mor M., Spadoni G., Tarzia G./titolo:Reassessing the melatonin pharmacophore--enantiomeric resolution, pharmacological activity, structure analysis, and molecular modeling of a constrained chiral melatonin analogue/doi:/rivista:Bioorganic & medicinal chemistry (Print)/anno:2006/pagina_da:3383/pagina_a:3391/intervallo_pagine:3383–3391/volume:14

3-(Acetylaminomethyl)-2-(ethoxycarbonyl)-6-methoxy-1,3,4,5-tetrahydrobenzo[cd]indole (2) is a rigid melatonin analogue that as a racemate displays about the same affinity and intrinsic activity of melatonin (1) in in vitro experiments. We report here

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::27f298ea7715d20482eb7bbf4d9d7365
http://www.cnr.it/prodotto/i/19618

Antioxydant and cytoprotective activioty og indole derivatives related to melatonin

Autor: Mor, M., Spadoni, G., Diamantini, G., Bedini, A., Tarzia, G., Silva, C., Vacondio, F., Rivara, M., Plazzi, P. V., Franceschini, D., Zusso, Morena, Giusti, Pietro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3657::b2b80b50fe246387f8bd9f3adb9debef
http://hdl.handle.net/11577/2472525