Výsledky vyhledávání - "Elena Gandini"

Akademický článek

Persistence to rivaroxaban therapy for stroke prevention in clinical practice in Italy: Rationale and design of the RITMUS-AF prospective observational cohort study

Autor: Gian Piero Perna, Pareen Vora, Elena Gandini, Claudia Francesca Lusona, Davide Tosarello

Publikováno v: International Journal of Cardiology: Heart & Vasculature, Vol 47, Iss , Pp 101229- (2023)

Background: Non-valvular atrial fibrillation (NVAF) is a cardiac rhythm disturbance that increases the risk of stroke and is highly prevalent in Europe and Italy, increasingly with advancing age. Oral anticoagulation is a key component of stroke prev

Externí odkaz: https://doaj.org/article/75803034474c45cabb1a65ed09f00db9

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Vitamin E protects human skeletal muscle from damage during surgical ischemia-reperfusion

Autor: Gian Paolo Novelli, Lucia Formigli, Alessandro Quattrone, Laura Papucci, Sergio Capaccioli, Elena Gandini, Chiara Adembri, Sandra Zecchi Orlandini, Carlo Pratesi, Lidia Ibba Manneschi

Publikováno v: The American Journal of Surgery. 173:206-209

Purpose The biochemical and morphological alterations induced in lower limb skeletal muscle by ischemia-reperfusion (I–R) during aortic surgery and the effect of vitamin E pretreatment were investigated. Methods Two groups of patients undergoing ao

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f42d76849327e47755c65e09d1e6193
https://doi.org/10.1016/s0002-9610(97)89593-1

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1H NMR and IR spectra of antitumour anthracyclines: Effect of the substitution pattern on the chemical shift values of the phenolic protons and on IR absorptions of the quinone system

Autor: Elena Gandini, Sergio Penco, Aristide Vigevani, Marzia Ballabio

Publikováno v: Magnetic Resonance in Chemistry. 23:344-352

1H NMR and IR data of numerous natural and synthetic analogues of daunorubicin and doxorubicin, anthracycline antibiotics successfully used in the clinical treatment of human tumours, have been recorded. The chemical shift values of the phenolic prot

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::88ad0584ef2e67b66518bff1aed86cdd
https://doi.org/10.1002/mrc.1260230513

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Azetidinone intermediates for the synthesis of cephem ring systems. Part 1. Chemical shift non-equivalence of the allylic methylene protons

Autor: Giorgio Palamidessi, Paolo Masi, Giovanni Franceschi, Elena Gandini, Maurizio Foglio, Antonino Suarato, A. Vigevani

Publikováno v: Journal of the Chemical Society, Perkin Transactions 1. :504

The chemical shift non-equivalence of the allylic methylene groups CH2Br and CH2SPh, present in some azetidinone intermediates useful for the synthesis of cephem ring systems, affords a valuable criterion for establishing the stereochemistry of the d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3ecd78acd0193dada9aebc14be185be0
https://doi.org/10.1039/p19790000504

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