Search Results - "CHIEPPA, S"

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    Carbon nanotube/nanodiamond structures: An innovative concept for stable and ready-to-start electron emitters by Guglielmotti, V., Chieppa, S., Orlanducci, S., Tamburri, E., Toschi, F., Terranova, M. L., Rossi, M.

    Published in Applied physics letters (30-11-2009)
    “…Efficient and robust cold cathodes have been assembled using as emitting material mats of single wall carbon nanotubes (SWCNTs) coated with nanodiamonds. The…”
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    Journal Article
  2. 2

    Carbon nanotube/nanodiamond structures: An innovative conceptfor stable and ready-to-start electron emitters by Guglielmotti, V., Chieppa, S., Orlanducci, S., Tamburri, E., Toschi, F., Terranova, M. L., Rossi, M.

    Published in Applied physics letters (03-12-2009)
    “…Efficient and robust cold cathodes have been assembled using as emitting material mats of single wall carbon nanotubes (SWCNTs) coated with nanodiamonds. The…”
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    Journal Article
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    Antagonistic effects of guanabenz, carteolol, and muzolimine on hypertensive responses in the anesthetized dog by Marmo, E, Lampa, E, Chieppa, S, Bile, G, Romano, A R, Vacca, C, Spadaro, R

    “…In dogs, treatment with guanabenz, carteolol, and muzolimine for 7 days, reduced the blood pressure responses to bilateral occlusion of the carotid arteries,…”
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    Journal Article
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    Experimental analysis of some cardiovascular effects of Verapamil by Marmo, E, Coscia, L, Rossi, F, Chieppa, S, Brita, G, Caputi, A P

    Published in Minerva medica (23-05-1975)
    “…In vivo and in vitro experiments showed that Verapamil dilates the coronaries, prevents coronary spasm, produces Ca++-antagonism, offers protection against…”
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    Derivatives of 1,3,3-trimethyl-6-azabicyclo[3.2.1]octane with hypotensive activity. I by Mariani, E, Bondavalli, F, Schenone, P, Ranise, A, Vacca, C, Chieppa, S, Spadaro, R, Marmo, E

    Published in Il Farmaco; edizione scientifica (01-09-1983)
    “…The synthesis of three series of glycinamides (IV), amides (V) and diamines (VI) starting from 1,3,3-trimethyl-6-azabicyclo[3.2.1]octane is described. Some of…”
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