Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Ventriglia V"'
Publikováno v:
Chemical Engineering Transactions, Vol 67 (2018)
The aim of the work is to develop a comparison between two software able to assess the risk associated with the transport of goods by road: QRAM - Quantitative Risk Assessment Model and GIIS – Global Integrated Information System, implemented withi
Autor:
PACIELLO, ORLANDO, PASOLINI, MARIA PIA, CIARAMELLA, PAOLO, RESTUCCI, BRUNELLA, PAPPARELLA, SERENELLA, POLITANO L, VENTRIGLIA V. M, PILUSO G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::26b756d2a76f4e7f45f556fee6490e17
http://hdl.handle.net/11588/109288
http://hdl.handle.net/11588/109288
Autor:
POLITANO, Luisa, NIGRO, Vincenzo, PETRETTA V, PASSAMANO L, BELSITO, Angela, ESPOSITO MG, VENTRIGLIA V, AURINO S, PALLADINO A, COMI LI, NIGRO G.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::df97ddd69aaaa8e20e90eaf45f644912
http://hdl.handle.net/11591/212491
http://hdl.handle.net/11591/212491
Autor:
POLITANO, Luisa, NIGRO V, PETRETTA V, PASSAMANO L, PILUSO, Giulio, BELSITO, Angela, ESPOSITO MG, VENTRIGLIA V, AURINO S, PALLADINO A, COMI LI, NIGRO G.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::cbf761b3b712ea9c0bc9fa62672721db
http://hdl.handle.net/11591/212498
http://hdl.handle.net/11591/212498
Autor:
Rinaldi, F., Botta, A., Vallo, L., Contino, G., Morgante, A., Iraci, R., Claudio Catalli, Silvestri, G., Ventriglia, V. M., Politano, L., Novelli, G.
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Myotonic dystrophy type 1 (DM1) is the most frequently inherited neuromuscular disease in adults. It is a multisystemic disorder with major cardiac involvement most commonly represented by first-degree atrioventricular heart block (AVB), followed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::de7f66a634e83baaf5b638c9375d8fc6
http://hdl.handle.net/2108/10995
http://hdl.handle.net/2108/10995
Autor:
Milić, Astrid, Piluso, G., Ventriglia, V., D˘Amico, F., Kovač, Biserka, Trlaja, Anuska, Mitrović, Zoran, Zurak, Niko, Politano, L., Canki-Klain, Nina
Beckground.Our previous results based on analysis of 28 patients from 18 families showed that 23 of 36 CAPN3 chromosomes(63, 8%) have 550delA mutation, and Y537X mutation in one family. Here we report the results of additional eight families together
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::096d9f4895ec6d704f0558beeba4379f
https://www.bib.irb.hr/222723
https://www.bib.irb.hr/222723
Autor:
Meznaric-Petrusa, Mmp, Zidar, J., Zupancic, N., Fanin, M., Corrado Angelini, Piluso, G., Ventriglia, V., Politano, L.
Publikováno v:
Web of Science
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a9613284515dc462271c1a4f12c25006
http://hdl.handle.net/11591/175441
http://hdl.handle.net/11591/175441