85 results on '"Piscopo G"'
Search Results
2. Reverse Mortgages: Risks and Opportunities
- Author
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Di Lorenzo, E., Piscopo, G., Sibillo, M., Tizzano, R., Land, Kenneth C., Series Editor, Skiadas, Christos H., editor, and Skiadas, Charilaos, editor
- Published
- 2020
- Full Text
- View/download PDF
3. Addressing the economic and demographic complexity via a neural network approach: risk measures for reverse mortgages
- Author
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Di Lorenzo, E., primary, Piscopo, G., additional, and Sibillo, M., additional
- Published
- 2023
- Full Text
- View/download PDF
4. Optimal cashback in a cooperative framework for peer-to-peer insurance coverages
- Author
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Clemente, Gian Paolo, Levantesi, S., Piscopo, G., Clemente G. P. (ORCID:0000-0001-6795-4595), Clemente, Gian Paolo, Levantesi, S., Piscopo, G., and Clemente G. P. (ORCID:0000-0001-6795-4595)
- Abstract
The challenges of using technology in the insurance field are opening new horizons for developing and distributing innovative products. Among these, peer-to-peer insurance schemes attract the interest of policyholders and insurance companies. Different types of peer-to-peer insurance have been introduced, from pure models to hybrid ones, as in the case of the broker model. In this paper, we focus on the broker model, where the groups of peers are formed by an insurance broker according to similar risk characteristics. The participants in the network pay an initial contribution defined by a cooperative rule that must be transparent and shared. A part or the whole of the collected contributions is set aside in a common fund. At the end of the year, if the common fund is sufficient to pay for the claims, the members obtain the excess over-retained premiums that is shared according to a capital allocation rule. We propose a cashback distribution mechanism based on the participant’s marginal contribution to the risk, framing the issue in a cooperative game and applying the concept of Shapley value to define an optimal allocation rule of the remaining capital. A numerical application based on a portfolio of motor third-party liability policies is developed to show how the model works
- Published
- 2023
5. Urinary epidermal growth factor/monocyte chemotactic peptide 1 ratio as non-invasive predictor of Mayo clinic imaging classes in autosomal dominant polycystic kidney disease
- Author
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Rocchetti, M.T., Pesce, F., Matino, S., Piscopo, G., Bari, I. di, Trepiccione, F., Capolongo, G., Perniola, M.A., Song, X.W., Khowaja, S., Haghighi, A., Peters, D., Paolicelli, S., Pontrelli, P., Netti, G.S., Ranieri, E., Capasso, G., Moschetta, M., Pei, Y., Gesualdo, L., Studio PRE MED MED PREcisione Prog, Rocchetti, Maria Teresa, Pesce, Francesco, Matino, Silvia, Piscopo, Giovanni, di Bari, Ighli, Trepiccione, Francesco, Capolongo, Giovanna, Perniola, Maria Antonietta, Song, Xuewen, Khowaja, Saima, Haghighi, Amirreza, Peters, Dorien, Paolicelli, Simona, Pontrelli, Paola, Netti, Giuseppe Stefano, Ranieri, Elena, Capasso, Giovambattista, Moschetta, Marco, Pei, York, and Gesualdo, Loreto
- Subjects
EGF/MCP1 ,CKD progression urine biomarker ,Nephrology ,MCP1 ,Risk prediction ,ADPKD ,EGF ,CKD progression urine biomarkers - Abstract
Background Age- and height-adjusted total kidney volume is currently considered the best prognosticator in patients with autosomal dominant polycystic kidney disease. We tested the ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 for the prediction of the Mayo Clinic Imaging Classes. Methods Urinary epidermal growth factor and monocyte chemotactic peptide 1 levels were measured in two independent cohorts (discovery, n = 74 and validation set, n = 177) and healthy controls (n = 59) by immunological assay. Magnetic resonance imaging parameters were used for total kidney volume calculation and the Mayo Clinic Imaging Classification defined slow (1A–1B) and fast progressors (1C–1E). Microarray and quantitative gene expression analysis were used to test epidermal growth factor and monocyte chemotactic peptide 1 gene expression. Results Baseline ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 correlated with total kidney volume adjusted for height (r = − 0.6, p r = 0.69 p p r = − 0.51, p 132 (100% slow) and p = 6.51E−16). Further, the ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 at baseline showed a positive correlation (p = 0.006, r = 0.36) with renal outcome (delta-estimated glomerular filtration rate per year, over a mean follow-up of 4.2 ± 1.2 years). Changes in the urinary epidermal growth factor and monocyte chemotactic peptide 1 were mirrored by gene expression levels in both human kidney cysts (epidermal growth factor: − 5.6-fold, fdr = 0.001; monocyte chemotactic peptide 1: 3.1-fold, fdr = 0.03) and Pkd1 knock-out mouse kidney (Egf: − 14.8-fold, fdr = 2.37E-20, Mcp1: 2.8-fold, fdr = 6.82E−15). Conclusion The ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 is a non-invasive pathophysiological biomarker that can be used for clinical risk stratification in autosomal dominant polycystic kidney disease.
- Published
- 2022
6. Predicting the Second Wave of COVID-19 Pandemic Through the Dynamic Evolving Neuro Fuzzy Inference System
- Author
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Levantesi, S., Nigri, A., and Piscopo, G.
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fuzzy systems ,adaptive algorithm ,COVID-19 ,predictive methods - Published
- 2022
7. Poster session 6: Saturday 6 December 2014, 08: 30–12: 30Location: Poster area
- Author
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Coppola, C, Piscopo, G, Rea, D, Maurea, C, Caronna, A, Capasso, I, and Maurea, N
- Published
- 2014
8. Poster session 4: Friday 5 December 2014, 08: 30–12: 30Location: Poster area
- Author
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Coppola, C, Piscopo, G, Galletta, F, Maurea, C, Esposito, E, Barbieri, A, and Maurea, N
- Published
- 2014
9. FAECAL EVALUATION OF PDG IN A FEMALE OKAPI (Okapia Johnstoni) TO DEFINE OESTRUS CYCLE AND FERTILE WINDOW FOR REPRODUCTION PROGRAM OF CONSERVATION
- Author
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Andreini, R., Zaccaroni, A., Piccinini, R., Piscopo, G., Andreini, R., Zaccaroni, A., Piccinini, R., and Piscopo, G.
- Subjects
hormones ,oestru ,Okapi ,PDG - Abstract
FAECAL EVALUATION OF PDG IN A FEMALE OKAPI (NOME SCIENTIFICO) TO DEFINE OESTRUS CYCLE AND FERTILE WINDOW FOR REPRODUCTION PROGRAM OF CONSERVATION Rebecca Andreini1,3, Annalisa Zaccaroni1, Renato-Piccinini,2 Giuseppe Piscopo3,4 1 DIMEVET Bologna University 2 Parco Zoo Falconara Marittima 3 Delfini Bizantini Research Association 4 Veterinary Medicine Naples University The okapi (Okapia Johnstoni) number is declining rapidly in their native habitat and the species is listed as endangered in the IUCN red list. To increase conservation efforts and to improve the welfare of okapis under human care, the evaluation of endocrine profile is an essential part of the scientific research. The need to use a non-invasive matrix for the endocrine analysis in wild life species is linked to the difficulty in obtaining blood samples and to the necessity to not stress the animals with restraining and medical procedure that could affect their welfare. This study aims to evaluate the faecal concentration of pregnanediol-3-glucoronide (PDG) in faeces of a young female hosted in Falconara Marittima zoo, Italy. Faeces have been collected twice a week, immediately after the emission, by zoo staff from March to April 2019. Samples have been labelled and stored at – 20 °C till analysis. For hormones extraction 200 μg of faeces have been weighted and added with 2 ml of ethanol, vortexed at 100 rpm for 60 minutes, centrifuged at 2500 rpm for 20 minutes and dried. For PDG detection an ELISA kit has been used, following test procedure. As far as we know few information are available regarding oestrous cycle and reproduction of the okapi, so a comparison of our results with bibliographic data was difficult. Despite this, we analysed our results in order to define the different phases of the oestrous cycle and to estimate their length with the goal to identify the fertile window of the subject. The results will allow scientists to have a further knowledge of the physiology of this species and will represent an essential step to define best strategies for the management of the subjects under human care and to establish programmes to strengthen the effort in assisted reproduction.
- Published
- 2019
10. DIETETIC AND TOXICOLOGICAL PARAMETERS EVALUATION IN AONYX CINEREUS
- Author
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ANDREINI, R., PISCOPO, G., CAVEDO, B., ZACCARONI, A., ANDREINI, R., PISCOPO, G., CAVEDO, B., and ZACCARONI, A.
- Subjects
RENAL DISEASE ,TRACE ELMENTS ,OTTER ,CALCIUM ,DIET - Abstract
Aonyx cinereus is the smallest otter existing, listed as Vulnerable under IUCN red list. Data on diet and nutritional intake of this species in the wild are scarce. Despite this, one of the most important parameters in the management of Aonyx cinereus in captivity, is the development of an appropriate diet program. The diet should meet nutritional needs of animals, guarantee an adequate intake of essential trace elements and be free from non-essential metals that could induce harmful effects. The three subjects included in this study arrived to Maitine Zoo few months ago and are the first specimens hosted in the park. For those reasons, we collected samples of food and faces of otters on weekly basis for 7 weeks, evaluating protein, lipidic and caloric content of the daily food rations of the animals. Moreover, we analysed concentration of trace elements in food and faeces, to define if the diet is balanced and safe and to acquire information about the metabolic processes of clawed otters. This study provides scientific data on Aonyx cinereus nutritional needs, metabolism and possible exposure to detrimental contaminants, giving useful information to implement the welfare and the health status of clawed otters under human care.
- Published
- 2019
11. Efficacy of self-monitoring blood glucose as a key component of a chronic care model versus usual care in type 2 diabetes patients treated with oral agents: results of a randomized trial
- Author
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Musacchio, N, Ciullo, I, Scardapane, M, Giancaterini, A, Pessina, L, Maino, S, Gaiofatto, R, Nicolucci, A, Rossi, M, Valentini, U, Cimino, A, Agosti, B, Zarra, E, Magri, A, Pellegrini, M, Pellarini, L, Sciangula, L, Nappi, F, Ciucci, A, Grassa, B, De Marco, R, Olivo, E, Trevisan, R, Frosio, I, Morlini, C, Corsi, A, Dodesini, A, Grassi, G, Calvi, E, Capello, E, Gramaglia, E, Ramella, V, De Rossi, C, Mengozzi, G, Orsi, E, Lunati, M, Palmieri, E, Resi, V, Grancini, V, Giarratana, L, Ragonese, M, Slongo, R, Scoponi, C, Tonolo, G, Amadori, G, Becciu, A, Canu, L, Cherchi, S, Paciotti, V, Alfidi, P, Babini, A, Ripani, R, Cantelli, R, Rossi, P, Di Cianni, G, Russo, L, Lemmi, P, Sannino, C, Marconi, S, Di Bartolo, P, Pellicano, F, Scolozzi, P, Annese, S, Lorizzo, F, Coppolino, A, Peditto, G, De Feo, M, Piscopo, G, Varriale, A, De Candia, L, Ceci, A, Elia, G, Falzone, G, Schembari, R, Citro, G, Di Mauro, M, D'Urso, C, Caruso, C, Musacchio N., Ciullo I., Scardapane M., Giancaterini A., Pessina L., Maino S., Gaiofatto R., Nicolucci A., Rossi M. C., Valentini U., Cimino A., Agosti B., Zarra E., Magri A., Pellegrini M. A., Pellarini L., Sciangula L., Nappi F., Ciucci A., Grassa B., De Marco R., Olivo E. S., Trevisan R., Frosio I., Morlini C., Corsi A., Dodesini A. R., Grassi G., Calvi E., Capello E., Gramaglia E., Ramella V., De Rossi C., Mengozzi G., Orsi E., Lunati M. E., Palmieri E., Resi V., Grancini V., Giarratana L., Ragonese M., Slongo R., Scoponi C., Tonolo G., Amadori G., Becciu A., Canu L., Cherchi S., Paciotti V., Alfidi P., Babini A., Ripani R., Cantelli R., Rossi P., Di Cianni G., Russo L., Lemmi P., Sannino C., Marconi S., Di Bartolo P., Pellicano F., Scolozzi P., Annese S., Lorizzo F., Coppolino A., Peditto G. C., De Feo M. E., Piscopo G., Varriale A., De Candia L., Ceci A., Elia G., Falzone G., Schembari R., Citro G., Di Mauro M., D'Urso C., Caruso C., Musacchio, N, Ciullo, I, Scardapane, M, Giancaterini, A, Pessina, L, Maino, S, Gaiofatto, R, Nicolucci, A, Rossi, M, Valentini, U, Cimino, A, Agosti, B, Zarra, E, Magri, A, Pellegrini, M, Pellarini, L, Sciangula, L, Nappi, F, Ciucci, A, Grassa, B, De Marco, R, Olivo, E, Trevisan, R, Frosio, I, Morlini, C, Corsi, A, Dodesini, A, Grassi, G, Calvi, E, Capello, E, Gramaglia, E, Ramella, V, De Rossi, C, Mengozzi, G, Orsi, E, Lunati, M, Palmieri, E, Resi, V, Grancini, V, Giarratana, L, Ragonese, M, Slongo, R, Scoponi, C, Tonolo, G, Amadori, G, Becciu, A, Canu, L, Cherchi, S, Paciotti, V, Alfidi, P, Babini, A, Ripani, R, Cantelli, R, Rossi, P, Di Cianni, G, Russo, L, Lemmi, P, Sannino, C, Marconi, S, Di Bartolo, P, Pellicano, F, Scolozzi, P, Annese, S, Lorizzo, F, Coppolino, A, Peditto, G, De Feo, M, Piscopo, G, Varriale, A, De Candia, L, Ceci, A, Elia, G, Falzone, G, Schembari, R, Citro, G, Di Mauro, M, D'Urso, C, Caruso, C, Musacchio N., Ciullo I., Scardapane M., Giancaterini A., Pessina L., Maino S., Gaiofatto R., Nicolucci A., Rossi M. C., Valentini U., Cimino A., Agosti B., Zarra E., Magri A., Pellegrini M. A., Pellarini L., Sciangula L., Nappi F., Ciucci A., Grassa B., De Marco R., Olivo E. S., Trevisan R., Frosio I., Morlini C., Corsi A., Dodesini A. R., Grassi G., Calvi E., Capello E., Gramaglia E., Ramella V., De Rossi C., Mengozzi G., Orsi E., Lunati M. E., Palmieri E., Resi V., Grancini V., Giarratana L., Ragonese M., Slongo R., Scoponi C., Tonolo G., Amadori G., Becciu A., Canu L., Cherchi S., Paciotti V., Alfidi P., Babini A., Ripani R., Cantelli R., Rossi P., Di Cianni G., Russo L., Lemmi P., Sannino C., Marconi S., Di Bartolo P., Pellicano F., Scolozzi P., Annese S., Lorizzo F., Coppolino A., Peditto G. C., De Feo M. E., Piscopo G., Varriale A., De Candia L., Ceci A., Elia G., Falzone G., Schembari R., Citro G., Di Mauro M., D'Urso C., and Caruso C.
- Published
- 2018
12. Leadership e clima organizzativo
- Author
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Adinolfi, P., de Gennaro, D., and Piscopo, G.
- Subjects
Leadership ,Clima organizzativo - Published
- 2020
13. Quality Evaluation of Bank Credit: Empirical Evidence Using Logistic Regression Model
- Author
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Piscopo G., Mattera R., Giacalone M., Piscopo, G., Mattera, R., and Giacalone, M.
- Subjects
logit model ,regression model ,credit analysi ,odds ratio ,Credit scoring ,Credit scoring, logit model, credit analysis, regression model, odds ratio - Abstract
Consumer credit today has become an important form of diversification in the banking offer and it is a fundamental tool for the acquisition of new customers. The assessment of credit risk and therefore the reliability of the customer, is a fundamental aspect which needs to be explored because it has direct influences both on the level of the interest rates applied on the loan and on the timing of credit disbursement, with strong implications on customer satisfaction. There are various methods which can be used in the field of credit scoring including those of a statistical nature. One of the most used model is the logit one. The purpose of this paper is to provide empirical evidence about the application of the logistic model in the analysis of credit scoring.
- Published
- 2018
14. Glomerular filtration rate: A prognostic marker in atrial fibrillation—A subanalysis of the AntiThrombotic Agents Atrial Fibrillation
- Author
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Proietti, Riccardo, Gonzini, Lucio, Pizzimenti, Giovanni, Ledda, Antonietta, Sanna, Pietro, Alturki, Ahmed, Russo, Vincenzo, Lencioni, Mauro, Siciliano, R., Boffa, M., Bazzanini, F., Di Nucci, G., Fonti, S., De Franceschi, T., Davio, P., Alagna, G., Cipollini, F., Arma, P., Gunnellini, M. G., Dottori, M., Paulillo, D., Giudice, M., Sicuro, M., Lenti, S., Iannelli, G., Notarstefano, P., Galiotto, M., Apolloni, Enzo, Molini, G., Massarelli, L., Di Iorio, P., Scandurra, F., Candelmo, F., Iodice, P., Laureano, R., Perlangeli, S., Praticò, A., Lucchesi, Q., Conese, V., Scalera, G., Palma, F., De Antoni, M. E., Beltramello, G., Carbonella, M., Capone, A., Bianchi, V., Zerella, F., Masina, M., Boggian, G., Pancaldi, L. G., Brucato, A. L., Scialfa, S., Ferrari, P., Gavazzi, A., Santoro, E., Bertinieri, G., Caragnano, V., Zaccaroni, S., Marchetti, G., Urbinati, S., Belmonte, G., Giannoni, C., Panuccio, D., Pedone, V., Colletta, M., Di Pasquale, G., Cemin, R., Paffoni, P. R. C., Pezzotti, Chiara, Capretti, M., Lamari, A. L., Maugeri, S., Moretti, R., Ganga, R., Mascia, P., Caddori, A., Cusumano, S., Alletto, M., DE VINCENZO, Ciro, Musacchio, E., Stendardo, A., Cantarella, SALVATORE ALFREDO, Ferrari, V., Bassano, F., PERRONE CAPANO, Carla, Piccinni, G. C., Catanzaro, M., Vinciguerra, A., Lusiani, L., De Caro, G., Scarcia, M., Scarcia, Aurora, Losi, E., Gaddi, O., Lo Sciuto, A., Cascio Ingurgio, N., Vignai, E., Romano, M., Borzì, V., Bellanuova, I. A., Felis, S., Gulizia, M. M., Francese, G. M., Artale, S., Mazzuca, S., Perticone, F., Tirotta, D., Talini, E., Ventrella, F., Iosa, G., Cuccurullo, O., Bertello, P. D., Benemio, G., Garognoli, O., Arcelli, G., Prosciutti, L., De Matthaeis, G., Quattrini, C., Calcagno, S., Canestrini, S., Franco, A., Pastorelli, R., Acquati, F., Botto, G. L., Sitta, N., Migliacci, R., Cosmi, F., Tarquini, B., Chiappetta, P., Sprovieri, M. F., Macrì, G., Bertolazzi, S., Spotti, Alessia, Pirelli, S., Marasco, M. F., Elia, Martina, Gambino, G. M., Fenoglio, L., Gelmini, G. P., Ziacchi, V., Rigon, N., Petix, N. R., Zipoli, A., Caiolo, A., Marino, E., Scattolin, G., Gerini, S., Parisi, G., Tavernese, G., Conti, Alessandro, Ferrante, Federico, Morettini, A., Alterini, B., Rocchi, Federico, Nozzoli, C., Goedecke, L., Seravalle, C., Cuomo, A., Panettieri, I., Pellegrino, P., Di Biase, M., Savarese, G., Patriarchi, F., Bondì, Giuseppina, Rossini, Elena, Nello, S., Ranieri, A. T., Gelonesi, F. N., Costantini, M., Dugnani, M., Ria, L., Mussardo, V., Zanini, G., Morgante, O., Fazio, G., Lo, G., Castello, C., Moroni, L. A., Costa, S., Domenicucci, S., Venzano, C., Loiacono, L., Ortuso, R., Esposito, L., Cuzzucrea, D. G., Fiammengo, F., Selva, E., Gestra, R., Alessandri, M., Nuzzi, G., Porrino, L., Parise, P., Capponi, E. A., Mandorla, S., Politi, Caterina, Olivieri, Claudia, Gurioli, L., Agostinelli, P., Striuli, R., Petrarca, Massimo, Corsini, Francesca, Orlandini, F., Badolati, S., Colarusso, D., Vertullo, V., Pelaggi, P., Campagna, G., Haupt, E., Parente, F., Milanese, G., Magliari, F., Morando, G., Guarise, P., Mazzone, A., Palumbo, G., Lambelet, P., Camaiti, A., Pasquinelli, P., Frediani, L., Vituliano, A., Brunelleschi, G., Lisi, C., La Torre, P. P. A., Villella, A., Rimoldi, A., Russo, V., Di Summa, F., Reggiani, A., Raimondo, F. C., Disalvo, D., Borrello, V. M., Magnante, A., Stellitano, E., Procopio, L., Franculli, F., Serafini, Filippo, Tondo, C., Fiorentini, C., Manfredini, R., Robbiolo, L., Pizzimenti, G., VASQUEZ LOPEZ, LUIDER FERNEY, Piangiamore, A., Tosi, P., Donà, G., Bacchiega, E., Malavasi, V., Modena, M. G., Divella, C., Marengo, C., Montanari, P., Manicardi, V., Abate, L., Cuccuini, A., Magni, S., Vincenti, A., Spinelli, M., Mortara, A., Specchia, G., Silvestri, N., Silvestri, Oriana, Piscopo, G., Muscherà, R., Gallucci, F., Cannavale, A., Bresciani, A., Perrone Filardi, P., Fontanella, Andrea, Iannuzzo, D., Lucà, S., Zuccoli, A., Rinaldi, P., Ferri, G., Barbieri, E., Grasselli, S., Rossi, A., Agosti, S., Sanna, GIAN PAOLO, Casu, G., Orecchioni, G., Da Silva Carvalho, P. C., POZZI MUCELLI, Roberto, Salvati, Fabio, Bendini, M. G., Giordano, G., Pellegrini, F., Pighini, G., Tremolada, F., Zanin, L., Ledda, A., Floresta, A. M., Enia, F., Nicolosi, G., Ingrillì, F., D'Angelo, A., Musacchio, D., Savastano, Silvia, Magnani, Leonardo, Capitelli, M., Cioni, Giovanni, Aloisi, B., De Finis, A., Vacri, A., Costantini, V., Guercini, F., Zingarini, G., Nardoni, M. C., Teghini, L., Panigada, G., Di Marco, S., Vergoni, W., Paonessa, K., Artom, A., Bigliardi, M., Riccardi, R., Riva, L., Marandino, A., Barsotti, L., Ginocchio, G., Marchese, Dario, Tintori, G., Annese, M., Breschi, R., Manini, M., Scopelliti, Giulia, Pastore, A., Spirito, G., Amato, A., Del Bianco, F., Ongari, M., Fiorencis, R., Querci, F., Martone, V. D., Molero, U., Fiusti, R., Giovannini, T., D'Arienzo, E., Cellamare, G., Placci, A., Gulli, G., Ruggeri, A., Pulitanò, G., Iori, I., Ingianni, N., Saporito, D., Marconi, GIAN MARIA, Grossi, Alice, Grosseto, D., Ciamei, M., Mete, F., Russo, F., Bianchi, C., Costantino, S., Manfellotto, D., Risa, M. P., Azzolini, P., Conversano, L., Santini, M., Macchiusi, A., Francia, P., Pietrantonio, F., Biscione, F., Magliano, G., Fedele, Francesca, Salituri, S., Salituri, F., Zamboni, S., Rossetti, C., Roncon, Leonora, Delucchi, M., De Benedictis, M., Vitolo, A., Anselmi, Michela, Celino, T., Moretti, V., Cuccurullo, M., Castelli, G., Martino, G., Pierandrei, G., Carella, A. M., Tonizzo, M., Nassi, R., Tarducci, R., Fronticelli Baldelli, M., Commisso, B., Lazzarini, D., Matarazzo, M. M., Novati, P., Petacchi, R., Maninchedda, P., Melandri, F., Bellesi, P., Sacchetti, C., Grandi, M., Cattana, A., Tassara, R., Menardo, G., Aykut, V., Chesi, G., Reverzani, A., Galgano, Angela, Bartone, B., Stornello, M., Muscio, G., Gemmiti, M. P., Alfonsi, F., Fontana, D., Astarita, C., Gaspardo, G., La Brocca, A., Rillo, M., Pascente, T., Pirozzi, M. R., Addis, L., De Siati, P., Beato, E., Iannaccone, V., Barabani, M., Castronuovo, M., Battaia, L., Biscottini, B., Boccali, A., Marengo, S., Dallerba, R., Diana, A., Coser, Alessandra, Pauletto, P., Calzolari, V., Olivari, Z., De Masi De Luca, G., Accogli, M., Gerloni, R., Cattin, Laura, Vitali Serdoz, L., Sinagra, G., Bulfoni, A., DE BIASIO, Melissa, Proclemer, A., Miserocchi, F., Marazzi, R., SALERNO URIARTE, JORGE ANTONIO, Levantesi, G., Olivetti, P., Capuano, A., Bertoncelli, M. C., Molinaro, N., Anastasio, L., Teti, G., Vescovo, G. A., Muriago, M., Incao, F., Lettica, G. V., Nieswandt, V., Osti, R., Tafi, A., Proietti, Riccardo, Gonzini, Lucio, Pizzimenti, Giovanni, Ledda, Antonietta, Sanna, Pietro, Alturki, Ahmed, Russo, Vincenzo, Lencioni, Mauro, Siciliano, R., Boffa, M., Bazzanini, F., Di Nucci, G., Fonti, S., De Franceschi, T., Davio, P., Alagna, G., Cipollini, F., Arma, P., Gunnellini, M. G., Dottori, M., Paulillo, D., Giudice, M., Sicuro, M., Lenti, S., Iannelli, G., Notarstefano, P., Galiotto, M., Apolloni, E., Molini, G., Massarelli, L., Di Iorio, P., Scandurra, F., Candelmo, F., Iodice, P., Laureano, R., Perlangeli, S., Praticò, A., Lucchesi, Q., Conese, V., Scalera, G., Palma, F., De Antoni, M. E., Beltramello, G., Carbonella, M., Capone, A., Bianchi, V., Zerella, F., Masina, M., Boggian, G., Pancaldi, L. G., Brucato, A. L., Scialfa, S., Ferrari, P., Gavazzi, A., Santoro, E., Bertinieri, G., Caragnano, V., Zaccaroni, S., Marchetti, G., Urbinati, S., Belmonte, G., Giannoni, C., Panuccio, D., Pedone, V., Colletta, M., Di Pasquale, G., Cemin, R., Paffoni, P. R. C., Pezzotti, C., Capretti, M., Lamari, A. L., Maugeri, S., Moretti, R., Ganga, R., Mascia, P., Caddori, A., Cusumano, S., Alletto, M., De Vincenzo, C., Musacchio, E., Stendardo, A., Cantarella, S. A., Ferrari, V., Bassano, F., Perrone, C., Piccinni, G. C., Catanzaro, M., Vinciguerra, A., Lusiani, L., De Caro, G., Scarcia, M., Scarcia, A., Losi, E., Gaddi, O., Lo Sciuto, A., Cascio Ingurgio, N., Vignai, E., Romano, M., Borzì, V., Bellanuova, I. A., Felis, S., Gulizia, M. M., Francese, G. M., Artale, S., Mazzuca, S., Perticone, F., Tirotta, D., Talini, E., Ventrella, F., Iosa, G., Cuccurullo, O., Bertello, P. D., Benemio, G., Garognoli, O., Arcelli, G., Prosciutti, L., De Matthaeis, G., Quattrini, C., Calcagno, S., Canestrini, S., Franco, A., Pastorelli, R., Acquati, F., Botto, G. L., Sitta, N., Migliacci, R., Cosmi, F., Tarquini, B., Chiappetta, P., Sprovieri, M. F., Macrì, G., Bertolazzi, S., Spotti, A., Pirelli, S., Marasco, M. F., Elia, M., Gambino, G. M., Fenoglio, L., Gelmini, G. P., Ziacchi, V., Rigon, N., Petix, N. R., Zipoli, A., Caiolo, A., Marino, E., Scattolin, G., Gerini, S., Parisi, G., Tavernese, G., Conti, A., Ferrante, F., Morettini, A., Alterini, B., Rocchi, F., Nozzoli, C., Goedecke, L., Seravalle, C., Cuomo, A., Panettieri, I., Pellegrino, P., Di Biase, M., Savarese, G., Patriarchi, F., Bondi, G., Rossini, E., Nello, S., Ranieri, A. T., Gelonesi, F. N., Costantini, M., Dugnani, M., Ria, L., Mussardo, V., Zanini, G., Morgante, O., Fazio, G., Lo, G., Castello, C., Moroni, L. A., Costa, S., Domenicucci, S., Venzano, C., Loiacono, L., Ortuso, R., Esposito, L., Cuzzucrea, D. G., Fiammengo, F., Selva, E., Gestra, R., Alessandri, M., Nuzzi, G., Porrino, L., Parise, P., Capponi, E. A., Mandorla, S., Politi, C., Olivieri, C., Gurioli, L., Agostinelli, P., Striuli, R., Petrarca, M., Corsini, F., Orlandini, F., Badolati, S., Colarusso, D., Vertullo, V., Pelaggi, P., Campagna, G., Haupt, E., Parente, F., Milanese, G., Magliari, F., Morando, G., Guarise, P., Mazzone, A., Palumbo, G., Lambelet, P., Camaiti, A., Pasquinelli, P., Frediani, L., Vituliano, A., Brunelleschi, G., Lisi, C., La Torre, P. P. A., Villella, A., Rimoldi, A., Russo, V., Di Summa, F., Reggiani, A., Raimondo, F. C., Disalvo, D., Borrello, V. M., Magnante, A., Stellitano, E., Procopio, L., Franculli, F., Serafini, F., Tondo, C., Fiorentini, C., Manfredini, R., Robbiolo, L., Pizzimenti, G., Vasquez, L., Piangiamore, A., Tosi, P., Donà, G., Bacchiega, E., Malavasi, V., Modena, M. G., Divella, C., Marengo, C., Montanari, P., Manicardi, V., Abate, L., Cuccuini, A., Magni, S., Vincenti, A., Spinelli, M., Mortara, A., Specchia, G., Silvestri, N., Silvestri, O., Piscopo, G., Muscherà, R., Gallucci, F., Cannavale, A., Bresciani, A., Perrone Filardi, P., Fontanella, A., Iannuzzo, D., Lucà, S., Zuccoli, A., Rinaldi, P., Ferri, G., Barbieri, E., Grasselli, S., Rossi, A., Agosti, S., Sanna, P., Casu, G., Orecchioni, G., Da Silva Carvalho, P. C., Pozzi, R., Salvati, F., Bendini, M. G., Giordano, G., Pellegrini, F., Pighini, G., Tremolada, F., Zanin, L., Ledda, A., Floresta, A. M., Enia, F., Nicolosi, G., Ingrillì, F., D'Angelo, A., Musacchio, D., Savastano, S., Magnani, L., Capitelli, M., Cioni, G., Aloisi, B., De Finis, A., Vacri, A., Costantini, V., Guercini, F., Zingarini, G., Nardoni, M. C., Teghini, L., Panigada, G., Di Marco, S., Vergoni, W., Paonessa, K., Artom, A., Bigliardi, M., Riccardi, R., Riva, L., Marandino, A., Barsotti, L., Ginocchio, G., Marchese, D., Tintori, G., Annese, M., Breschi, R., Manini, M., Scopelliti, G., Pastore, A., Spirito, G., Amato, A., Del Bianco, F., Ongari, M., Fiorencis, R., Querci, F., Martone, V. D., Molero, U., Fiusti, R., Giovannini, T., D'Arienzo, E., Cellamare, G., Placci, A., Gulli, G., Ruggeri, A., Pulitanò, G., Iori, I., Ingianni, N., Saporito, D., Marconi, M., Grossi, A., Grosseto, D., Ciamei, M., Mete, F., Russo, F., Bianchi, C., Costantino, S., Manfellotto, D., Risa, M. P., Azzolini, P., Conversano, L., Santini, M., Macchiusi, A., Francia, P., Pietrantonio, F., Biscione, F., Magliano, G., Fedele, F., Salituri, S., Salituri, F., Zamboni, S., Rossetti, C., Roncon, L., Delucchi, M., De Benedictis, M., Vitolo, A., Anselmi, M., Celino, T., Moretti, V., Cuccurullo, M., Castelli, G., Martino, G., Pierandrei, G., Carella, A. M., Tonizzo, M., Nassi, R., Tarducci, R., Fronticelli Baldelli, M., Commisso, B., Lazzarini, D., Matarazzo, M. M., Novati, P., Petacchi, R., Maninchedda, P., Melandri, F., Bellesi, P., Sacchetti, C., Grandi, M., Cattana, A., Tassara, R., Menardo, G., Aykut, V., Chesi, G., Reverzani, A., Galgano, A., Bartone, B., Stornello, M., Muscio, G., Gemmiti, M. P., Alfonsi, F., Fontana, D., Astarita, C., Gaspardo, G., La Brocca, A., Rillo, M., Pascente, T., Pirozzi, M. R., Addis, L., De Siati, P., Beato, E., Iannaccone, V., Barabani, M., Castronuovo, M., Battaia, L., Biscottini, B., Boccali, A., Marengo, S., Dallerba, R., Diana, A., Coser, A., Pauletto, P., Calzolari, V., Olivari, Z., De Masi De Luca, G., Accogli, M., Gerloni, R., Cattin, L., Vitali Serdoz, L., Sinagra, G., Bulfoni, A., De Biasio, M., Proclemer, A., Miserocchi, F., Marazzi, R., Salerno Uriarte, J. A., Levantesi, G., Olivetti, P., Capuano, A., Bertoncelli, M. C., Molinaro, N., Anastasio, L., Teti, G., Vescovo, G. A., Muriago, M., Incao, F., Lettica, G. V., Nieswandt, V., Osti, R., and Tafi, A.
- Subjects
Male ,medicine.medical_specialty ,Time Factors ,Clinical Investigations ,Renal function ,030204 cardiovascular system & hematology ,Risk Assessment ,03 medical and health sciences ,0302 clinical medicine ,Fibrinolytic Agents ,Risk Factors ,atrial fibrillation ,glomerular filtration rate ,mortality ,Cardiology and Cardiovascular Medicine ,Internal medicine ,Antithrombotic ,medicine ,Humans ,In patient ,030212 general & internal medicine ,Renal Insufficiency ,Cardiovascular mortality ,Aged ,Retrospective Studies ,business.industry ,Incidence ,Atrial fibrillation ,General Medicine ,medicine.disease ,Prognosis ,Survival Rate ,Italy ,Hospital admission ,Atrial Fibrillation ,Female ,Follow-Up Studies ,Glomerular Filtration Rate ,Morbidity ,Cardiology ,business - Abstract
OBJECTIVE: An increased cardiovascular mortality and morbidity has been widely reported in patients with atrial fibrillation (AF). In this study, a subanalysis of the AntiThrombotic Agents Atrial Fibrillation (ATA‐AF) is performed with the aim to evaluate estimated glomerular filtration rate (eGFR) as an independent prognostic marker of cardiovascular mortality and morbidity in patients with AF. METHODS AND RESULTS: The ATA‐AF study enrolled 7148 patients with AF, in 360 Italian centers. The eGFR was calculated from data reported in patient notes or hospital database. This post‐hoc analysis included 1097 AF patients with eGFR data available and 1‐year clinical follow‐up. The endpoint was assessed as cardiovascular mortality and/or hospital admission for cardiovascular causes at follow‐up. Patients were also divided in two groups according to the eGFR (
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- 2018
15. Ecosystem of knowledge or knowledge contamination? An exploratory analysis at the boundaries of scientific domains
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Adinolfi, P, Capolupo, N, Giampaola, V, Palumbo, R, Piscopo, G, and Ruberto, M
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Knowledge ecosystem ,Settore SECS-P/10 - Organizzazione Aziendale ,Contamination ,Knowledge ecosystem, Interdisciplinary research, Scientific Knowledge ,Management ,Scientific Knowledge ,Interdisciplinary research - Published
- 2019
16. Myth #8: The Myth of Scale, Beyond Scale: The Quest for Quality
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Palumbo R, Piscopo G, Sampietro M, Martinez M, Moschera L, Mangia G, Scaramuccia D, Calvo A, Adinolfi Paola, Borgonovi Elio, Palumbo, R, Piscopo, G, Sampietro, M, Martinez, M, Moschera, L, Mangia, G, Scaramuccia, D, and Calvo, A
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- 2017
17. Antineoplastic-related cardiotoxicity, morphofunctional aspects in a murine model: contribution of the new tool 2D-speckle tracking
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Coppola C, Gennaro Riccio, Barbieri A, Mg, Monti, Piscopo G, Rea D, Arra C, Maurea C, De Lorenzo C, and Maurea N
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breast cancer ,cardiotoxicity ,ErbB2/Her2 ,immunotherapy ,Trastuzumab ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,doxorubicin ,lcsh:RC254-282 - Abstract
Carmela Coppola,1 Gennaro Riccio,1 Antonio Barbieri,2 Maria Gaia Monti,3 Giovanna Piscopo,1 Domenica Rea,2 Claudio Arra,2 Carlo Maurea,1 Claudia De Lorenzo,4,5 Nicola Maurea1 1Division of Cardiology, Istituto Nazionale per lo Studio e la Cura dei Tumori “Fondazione G. Pascale”, IRCCS, Naples, Italy; 2Animal Facility Unit, Department of Experimental Oncology, Istituto Nazionale per lo Studio e la Cura dei Tumori “Fondazione G. Pascale”, IRCCS, Naples, Italy; 3Department of Translational Medical Sciences, University Federico II, Naples, Italy; 4Department of Molecular Medicine and Medical Biotechnology, University Federico II, Naples, Italy; 5CEINGE Biotecnologie Avanzate, Naples, Italy Objective: Considering that global left ventricular systolic radial strain is a sensitive technique for the early detection of left ventricular dysfunction due to antineoplastics and the analysis of segmental myocardial contractility, we evaluated this technique for early detection of trastuzumab-related cardiotoxicity by comparing it with cardiac structural damage.Methods: Groups of six mice were injected with trastuzumab or doxorubicin, used either as single agents or in combination. Cardiac function was evaluated by transthoracic echocardiography measurements before and after treatment for 2 or 7 days, by using a Vevo 2100 high-resolution imaging system. After echocardiography, mice were euthanized, and hearts were processed for histological evaluations, such as cardiac fibrosis, apoptosis, capillary density, and inflammatory response.Results: Trastuzumab-related cardiotoxicity was detected early by 2D strain imaging. Radial strain was reduced after 2 days in mice treated with trastuzumab alone (21.2%±8.0% vs 40.5%±4.8% sham; P
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- 2016
18. Cardiac and Vascular Microenvironment: Biological and Clinical Implications in Cardiology
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Piscopo G, Maurea N, and Quagliariello
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Paracrine signalling ,Glycation ,business.industry ,Cancer research ,Medicine ,General Medicine ,business - Published
- 2018
19. 2018 Compendium of Radiation-Induced Effects for Candidate Particle Accelerator Electronics
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Danzeca, Salvatore, Foucard, Gilles, Tsiligiannis, Georgios, Ferraro, Rudy, Piscopo, G., McAllister, C.G., Borel, Thomas, Peronnard, Paul, Brugger, Markus, Masi, Alessandro, Gilardoni, Simone, European Organization for Nuclear Research (CERN), TEST (TEST), Laboratoire d'Informatique de Robotique et de Microélectronique de Montpellier (LIRMM), and Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)
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[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics - Abstract
International audience; The sensitivity of a variety of components for particle accelerators electronics has been analyzed against Single Event Effects, Total Ionizing Dose and Displacement Damage. The tested parts include analog, linear, digital and mixed devices.
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- 2018
20. Practical approach to patient therapy affected by Autosomal Dominant Autosomic Polycystic Kidney Disease
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Esposito, C., La Milia, V., Altobelli, C., Roberta Cerutti, Manunta, P., Dallera, N., Piscopo, G., Magistroni, R., Esposito, Ciro, La Milia, Vincenzo, Altobelli, Claudia, Cerutti, Roberta, Manunta, Paolo, Dallera, Nadia, Piscopo, Giovanni, and Magistroni, Riccardo
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Renal failure ,Cyst ,Autosomal Dominant Polycystic Kidney Disease ,tolvaptan ,Tolvaptan ,Practice Guidelines as Topic ,Humans ,Drug Interactions ,Aneurysm ,Polycystic Kidney, Autosomal Dominant ,Antidiuretic Hormone Receptor Antagonists - Abstract
The Autosomal Dominant Polycystic Kidney Disease(ADPKD) is the most frequent renal genetic condition and involves 7 to 10% of subjects undergoing renal replacement therapy. It is estimated that between 24,000 and 34,000 subjects in Italy are affected by this condition. For an illness that has long been neglected due to a lack of treatment options, an attractive treatment possibility is now available: tolvaptan has shown clinical efficacy regarding disease progression in two clinical trials (ADPKD patients with mild renal failure and ADPKD patients with advanced renal failure). The possible liver toxicity expressed in about 4% of the subjects exposed to the drug and an important aquaretic effect suggest prudence and attention in the use of this new molecule. Based on these critical points, some clinicians with direct experience in the use of the drug have briefly collected in the pages to follow the main clinical recommendations for the treatment of ADPKD patints. The recommendations concern the general approach to the patient affected by ADPKD but with particular attention to the aspects related to the new treatment. The delicate task of introducing the opportunities and limitations of the offered therapy to the patient will be deepened. Finally, the document wants to suggest how best to organize a clinic dedicated to this condition.
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- 2018
21. Radiation characterization of COTS MicroSD Memories for CERN applications
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Piscopo, G., primary, McAllister, C.G., additional, Tsiligiannis, G., additional, Danzeca, S., additional, and Masi, A., additional
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- 2019
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22. Low doses of Bisphenol A have pro-inflammatory and pro-oxidant effects, stimulate lipid peroxidation and increase the cardiotoxicity of Doxorubicin in cardiomyoblasts
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Quagliariello, V., primary, Coppola, C., additional, Mita, D.G., additional, Piscopo, G., additional, Iaffaioli, R.V., additional, Botti, G., additional, and Maurea, N., additional
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- 2019
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23. Prison theatre as an entrepreneurial opportunity: resilience, creativity and co-creation for inmates' rehabilitation
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Piscopo, G, Ambrosino, G, and Palumbo, R
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Settore SECS-P/10 - Organizzazione Aziendale ,Prison Theatre ,Value Co-Creation ,Social Entrepreneurship ,Social Rehabilitation ,Prison Theatre, Social Rehabilitation, Social Entrepreneurship, Value Co-Creation - Published
- 2017
24. Cardioprotection induced by ranolazine after trastuzumab treatment: the reduction of cardiotoxicity in vitro and in vivo study
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Maurea, N, Coppola, C, Piscopo, G, Galletta, F, Maurea, C, Rea, D, RICCIO, GENNARO, Maiolino, P, Arra, C, DE LORENZO, CLAUDIA, Maurea, N, Coppola, C, Piscopo, G, Galletta, F, Maurea, C, Rea, D, Riccio, Gennaro, Maiolino, P, Arra, C, and DE LORENZO, Claudia
- Published
- 2015
25. P616Cardioprotective effects of nanoemulsions loaded with natural anti-inflammatory molecules against doxorubicin-induced cardiotoxicity in cardiomyocytes
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Maurea, N, primary, Quagliariello, V, additional, Vecchione, R, additional, Di Cicco, C, additional, De Capua, A, additional, Coppola, C, additional, Piscopo, G, additional, Paciello, R, additional, Iaffaioli, R V, additional, Netti, P A, additional, and Botti, G, additional
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- 2018
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26. I percorsi di cura e la centralità del paziente
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Annarumma, C, Festa, G, Piscopo, G, and Palumbo, R
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Settore SECS-P/10 - Organizzazione Aziendale ,Organizzazione - Innovazione - Sanità - Published
- 2016
27. Theatre in prison as a virtual place of knowledge creation
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Piscopo, G, Palumbo, R, and Ambrosino, G
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Settore SECS-P/10 - Organizzazione Aziendale ,Prison theatre, social rehabilitation, Ba, knowledge creation ,social rehabilitation ,knowledge creation ,Prison theatre ,Ba - Published
- 2016
28. LCZ 696, administered during doxorubicin, trastuzumab or pertuzumab treatment, prevents cardiotoxicity in our in vitro model
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Maurea, N., primary, Paciello, R., additional, Piscopo, G., additional, Rienzo, A., additional, Sorrentino, G., additional, Maurea, C., additional, Caputo, R., additional, De Laurentiis, M., additional, Maiolino, P., additional, Coppola, C., additional, and De Lorenzo, C., additional
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- 2017
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29. Approfondimenti teorico–metodologici per Progetto T.R.E.E
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Annarumma, C, Di Giuditta Carmela, Palumbo, R, Piscopo, G, and Storlazzi, A
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Settore SECS-P/10 - Organizzazione Aziendale - Published
- 2015
30. Ranolazine partially blunts ado trastuzumab emtansine related cardiotoxicity
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Maurea, N., primary, Coppola, C., additional, Piscopo, G., additional, Riccio, G., additional, Rienzo, A., additional, Maurea, C., additional, Barbieri, A., additional, De Lorenzo, C., additional, and Iaffaioli, R.V., additional
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- 2016
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31. Cardiotoxic effects of the novel anti-ErbB2 agent ado trastuzumab emtansine
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Iaffaioli, R.V., primary, Coppola, C., additional, Piscopo, G., additional, Riccio, G., additional, Rienzo, A., additional, Maurea, C., additional, Barbieri, A., additional, De Lorenzo, C., additional, and Maurea, N., additional
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- 2016
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32. A Practical Approach for Management of QT Prolongation Induced by Anticancer Drugs
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Maurea, N., primary, Coppola, C., additional, Piscopo, G., additional, Galletta, F., additional, Riccio, G., additional, and De Lorenzo, C., additional
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- 2016
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33. Autosomal recessive polycystic kidney disease: Hepatic manifestations in relation to kidney failure
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Piscopo, G., primary, Carbone, V., additional, Melchionda, S., additional, Gesualdo, L., additional, and Giordano, M., additional
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- 2015
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34. 441 Relationship of serum high sensitivity C-reactive protein to metabolic syndrome and waist-hip ratio in cancer patients
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Maurea, N., primary, Quagliariello, V., additional, Coppola, C., additional, Piscopo, G., additional, Galletta, F., additional, Esposito, E., additional, Capasso, I., additional, and Iaffaioli, R.V., additional
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- 2015
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35. 811 Ranolazine reduces Trastuzumab toxicity in vitro and in vivo, when it is administered after anticancer treatment
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Maurea, N., primary, Coppola, C., additional, Piscopo, G., additional, Galletta, F., additional, Esposito, E., additional, Capasso, I., additional, Arra, C., additional, Riccio, G., additional, Lorenzo, C. De, additional, and Laurentiis, M. De, additional
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- 2015
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36. Proposal of a new method for the use of the Rydel–Seiffer tuning fork in the screening of diabetic polyneuropathy. A pilot study
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de Simone, R., primary, Rabitti, P.G., additional, De Feo, E.M., additional, Manguso, F., additional, Piscopo, G., additional, and Scionti, L., additional
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- 2015
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37. P059 Ranolazine administered after trastuzumab treatment prevents cardiotoxicity in mice
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Coppola, C., primary, Piscopo, G., additional, Galletta, F., additional, Maurea, C., additional, Rea, D., additional, Arra, C., additional, and Maurea, N., additional
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- 2015
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38. 400P - LCZ 696, administered during doxorubicin, trastuzumab or pertuzumab treatment, prevents cardiotoxicity in our in vitro model
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Maurea, N., Paciello, R., Piscopo, G., Rienzo, A., Sorrentino, G., Maurea, C., Caputo, R., De Laurentiis, M., Maiolino, P., Coppola, C., and De Lorenzo, C.
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- 2017
- Full Text
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39. Poster session 4
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Parisi, V, Ferro, G, Bevilacqua, A, Caruso, A, Grimaldi, G, Rengo, G, Leosco, D, Ferrara, N, Yan, B P Y, Lai, KH, Chan, MYT, Lam, DYY, Fong, KNY, Chau, C, Fok, MHL, Kam, K, Tam, GM, Lee, PW, Takeuchi, H, Angelis, A, Aggeli, K, Ioakeimidis, N, Felekos, I, Abdelrasoul, M, Aznaouridis, K, Rokas, K, Vlachopoulos, C, Tousoulis, D, Cano Carrizal, R, Casanova Rodriguez, C, Prieto Moriche, E, Iglesias Del Valle, D, Cadenas Chamorro, R, De Juan Baguda, J, Martin-Penato Molina, A, Paredes Gonzalez, B, Garcia Garcia, A, Plaza Perez, I, Caiani, EG, Arbeille, P, Massabuau, P, Colombo, F, Ferri, G, Kasswat, C, Medvedofsky, D, Lang, RM, Vaida, P, Kuznetsov, VA, Yaroslavskaya, EI, Krinochkin, DV, Pushkarev, GS, Gorbatenko, EA, Bruno, RM, Bianchini, E, Di Lascio, N, Stea, F, Ujka, K, Marabotti, A, Dangelo, GS, Ghiadoni, L, Pratali, L, Zemedkun, M, Wang, Z, Asch, FM, Niki, K, Sugawara, M, Yauchi, S, Inoue, K, Yagawa, M, Takamisawa, I, Umemura, J, Yoshikawa, T, Sumiyoshi, T, Tomoike, H, Christov, G, Saundankar, J, Perdreau, E, Mukasa, T, Shah, V, Klein, N, Brogan, P, Marek, J, Batalli, A, Ibrahimi, P, Ahmeti, A, Haliti, E, Bytyci, I, Poniku, A, Henein, MY, Bajraktari, G, Luo, XX, Fang, F, Gan, SF, Ma, Z, Yu, CM, Gonella, A, Conte, E, Morena, L, Riva, L, Civelli, D, Losardo, L, Canepari, ME, Castellino, C, Grasso, M, Margaria, F, Massoure, P L, Camus, O, Gabaudan, C, Desmots, F, Fourcade, L, Jacquier, A, Divchev, D, Weippert, M, Schmidt, P, Gettel, H, Neugebauer, A, Behrens, K, Braumann, K-M, Wolfarth, B, Nienaber, CA, Rodriguez Gonzalez, E, Monivas Palomero, V, Mingo Santos, S, Restrepo Cordoba, MA, Goirigolzarri Artaza, J, Gomez Bueno, M, Garcia Izquierdo, E, Serrano Fiz, S, Gonzalez Roman, A, Segovia Cubero, J, Pila-On, SASTRA, Atmadikoesoemah, C, Soesanto, A, Andriantoro, H, Kowallick, J T, Morton, G, Lamata, P, Jogiya, R, Kutty, S, Lotz, J, Hasenfuss, G, Nagel, E, Chiribiri, A, Schuster, A, Jung, IH, Moon, JG, Byun, YS, Kim, TH, Park, SH, Seo, HS, Wellnhofer, E, Kriatselis, C, 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Rodriguez Munoz, DA, Jimenez Nacher, JJ, Fernandez-Golfin, C, Zamorano, JL, Ongun, A, Habibova, U, Gerede, DM, Dincer, I, Kilickap, M, Erol, C, Nouhravesh, N, Andersen, HU, Jensen, JS, Rossing, P, Jensen, MT, Gasior, Z, Dabek, J, Balys, M, Glogowska-Rygus, J, and Pysz, P
- Abstract
Purpose: Epicardial adipose tissue (EAT) thickness, measured by echocardiography, is associated to the presence of coronary artery disease (CAD) and severe aortic stenosis (AS). EAT thickness is commonly referred as the diameter of the echo-free space between the right ventricular wall and the visceral layer of the pericardium in parasternal long axis view, using the aortic annulus as an anatomic landmark (EAT-1). We aimed to demonstrate that the direct measurement of the adipose tissue thickness visualized in the space between the ascending aorta and the right ventricle (EAT-2) might be considered an alternative method. Methods: We measured EAT-1 and EAT-2 in 130 pts with severe cardiac disease referred for cardiac surgery: 53 pts with isolated AS, 49 pts with severe CAD, and 28 pts with both severe AS and CAD (AS+CAD); and in 50 control subjects matched for age, sex and BMI. The two measurements were obtained at end-systole in 3 cardiac cycles (figure). Results. Both EAT-1 and EAT-2 measurements had an excellent reproducibility. With respect to controls pts had significantly increased EAT-1 (2,4 ± 0,5mm vs 6 ± 2mm; p<0,05) and EAT-2 (3 ± 1,2mm vs 12 ± 3mm; p<0,05). EAT-1 and EAT-2 were not statistically different in controls. EAT-2 was significantly higher than EAT-1 in CAD, AS, and AS+CAD pts (p<0,05). Interestingly, EAT-2, but not EAT-1, was significantly increased in AS+CAD pts with respect to EAT-2 of pts with isolated AS and isolated CAD. Conclusions: Our data demonstrate that EAT-2, as well as EAT-1, is a valuable method to measure EAT thickness. Further, EAT-2 seems to better recognize EAT increase, in pts with AS+CAD. Comprehensively, EAT-2 is greater than EAT-1. The larger space between ascending aorta and right ventricle, allowing EAT expansion, could justify our observation.
- Published
- 2015
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40. Poster session 6: Saturday 6 December 2014, 08:30-12:30 * Location: Poster area
- Author
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Goirigolzarri Artaza, J, Gallego Delgado, M, Jaimes Castellanos, CP, Cavero Gibanel, MA, Pastrana Ledesma, MA, Alonso Pulpon, LA, Gonzalez Mirelis, J, Al Ansi, R Z, Sokolovic, S, Cerin, G, Szychta, W, Popa, B A, Botezatu, D, Benea, D, Manganiello, S, Corlan, A, Jabour, A, Igual Munoz, B, Osaca Asensi, JOA, Andres La Huerta, AALH, Maceira Gonzalez, AMG, Estornell Erill, JEE, Cano Perez, OCP, Sancho-Tello, MJSTDC, Alonso Fernandez, PAF, Sepulveda Sanchez, PSS, Montero Argudo, AMA, Palombo, C, Morizzo, C, Baluci, M, Kozakova, M, Panajotu, A, Karady, J, Szeplaki, G, Horvath, T, Tarnoki, DL, Jermendy, AL, Geller, L, Merkely, B, Maurovich-Horvat, P, Group, MTA-SE "Lendület" Cardiovascular Imaging Research, Moustafa, S, Mookadam, F, Youssef, M, Zuhairy, H, Connelly, M, Prieur, T, Alvarez, N, Ashikhmin, Y, Drapkina, O, Boutsikou, M, Demerouti, E, Leontiadis, E, Petrou, E, Karatasakis, G, Kozakova, M, Morizzo, C, Bianchi, V, Marchi, B, Federico, G, Palombo, C, Chatzistamatiou, E, Moustakas, G, 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Garcia-Campos, A, Diaz, E, Martin, M, Rodriguez-Suarez, ML, Leon, V, Fidalgo, A, Moris, C, De La Hera, JM, Kylmala, M M, Rosengard-Barlund, M, Groop, P H, Lommi, J, Bruin De- Bon, HACM, Bilt Van Der, IA, Wilde, AA, Brink Van Den, RBA, Teske, AJ, Rinkel, GJ, Bouma, BJ, Teixeira, R, Monteiro, R, Garcia, J, Silva, A, Graca, M, Baptista, R, Ribeiro, M, Cardim, N, Goncalves, L, Duszanska, A, Skoczylas, I, Kukulski, T, Polonski, L, Kalarus, Z, Choi, J-H, Park, JS, Ahn, JH, Lee, JW, Ryu, SK, Ahn, J, Kim, DH, Lee, HO, Przewlocka-Kosmala, M, Mlynarczyk, J, Rojek, A, Mysiak, A, Kosmala, W, Pellissier, A, Larochelle, E, Krsticevic, L, Baron, E, Le, V, Roy, A, Deragon, A, Cote, M, Garcia, D, Tournoux, F, Yiangou, K, Azina, C, Yiangou, A, Zitti, M, Ioannides, M, Ricci, F, Dipace, G, Aquilani, R, Radico, F, Cicchitti, V, Bianco, F, Miniero, E, Petrini, F, De Caterina, R, Gallina, S, Jardim Prista Monteiro, R, Teixeira, R, Garcia, J, Baptista, R, Ribeiro, M, Cardim, N, Goncalves, L, Chung, H, Kim, JY, Joung, B, Uhm, JS, Pak, HN, Lee, MH, Lee, KY, Ragab, AM, Abdelwahab, AMIR, Yazeed, YASER, El Naggar, WAEL, Spahiu, K, Spahiu, E, Doko, A, Liesting, C, Brugts, JJ, Kofflard, MJM, Kitzen, JJEM, Boersma, E, Levin, M-D, Coppola, C, Piscopo, G, Rea, D, Maurea, C, Caronna, A, Capasso, I, Maurea, N, Azevedo, O, Tadeu, I, Lourenco, M, Portugues, J, Pereira, V, Lourenco, A, Nesukay, E, Kovalenko, V, Cherniuk, S, Danylenko, O, Muhammedov, MB, Ahmedova, DM, Hojakuliyev, BG, Atayeva, D, Nemes, A, Domsik, P, Kalapos, A, Lengyel, C, Varkonyi, TT, Orosz, A, Forster, T, Castro, M, Abecasis, J, Dores, H, Madeira, S, Horta, E, Ribeiras, R, Canada, M, Andrade, MJ, Mendes, M, Morosin, M, Piazza, R, Leonelli, V, Leiballi, E, Pecoraro, R, Cinello, M, Dell' Angela, L, Cassin, M, Sinagra, G, Nicolosi, GL, Wierzbowska-Drabik, K, Hamala, P, Kasprzak, JD, O'driscoll, J, Rossato, C, Gargallo-Fernandez, P, Araco, M, Sharma, S, Sharma, R, Jakus, N, Baricevic, Z, Ljubas Macek, J, Skoric, B, Skorak, I, Velagic, 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Minatoguchi, S, Houle, H, Warita, S, Ono, K, Noda, T, Watanabe, S, Minatoguchi, S, Cho, E J, Park, S J, Lim, H J, Chang, S A, Lee, S C, Park, S W, Cho, E J, Park, S J, Lim, H J, Chang, S A, Lee, S C, Park, S W, Mornos, C, Cozma, D, Ionac, A, Mornos, A, Popescu, I, Ionescu, G, Pescariu, S, Melzer, L, Faeh-Gunz, A, Seifert, B, Attenhofer Jost, C H, Storve, S, Haugen, BO, Dalen, H, Grue, JF, Samstad, S, Torp, H, Ferrarotti, L, Maggi, E, Piccinino, C, Sola, D, Pastore, F, Marino, PN, Ranjbar, S, Karvandi, M, Hassantash, SA, Karvandi, M, Ranjbar, S, Tierens, S, Remory, I, Bala, G, Gillis, K, Hernot, S, Droogmans, S, Cosyns, B, Lahoutte, T, Tran, N, Poelaert, J, Al-Mallah, M, Alsaileek, A, Nour, K, Celeng, CS, Horvath, T, Kolossvary, M, Karolyi, M, Panajotu, A, Kitslaar, P, Merkely, B, Maurovich Horvat, P, Group, MTA-SE "Lendület" Cardiovascular Imaging Research, Aguiar Rosa, S, Ramos, R, Marques, H, Portugal, G, Pereira Da Silva, T, Rio, P, Afonso Nogueira, M, Viveiros Monteiro, A, Figueiredo, L, and Cruz Ferreira, R
- Abstract
Introduction: The increase of left auricular volume (LAV) is a robust cardiovascular event predictor. Despite that echochardiography is more often used, cardiac MRI is considered more accurate. Our objetives are to validate "fast" LAV measures by MRI vs the considered gold standard (GS) and to compare Echo and MRI in a wide spectrum of patients. Methods: In a non-selected popullation with MRI study previously realized, we measured LAV by biplane method (BPMR) and by area-length in 4 chamber view (ALMR) and compared them with biplane (BPe) and discs method (MDDe) in 4 chamber view in echo. To validate MRI measurements, we measured LAV in short axis slices (Simpson Method, SM) in a group of patients and considered it the GS. Results: 186 patients were included (mean age 51 ± 17 age; 123 male; 14 in AF) with clinical indication of cardiac MRI (Philips 1,5 T). In 24 patients SM was calculated. 29% of cardiac MRI were considered normal. Mean underlying pathologies were myocardiopathy (27%), Ischemic myocardiopathy (17%), myopericarditis (10%), prior to AF ablation (4%), valvular disease (6%) and miscellaneous (7%). Excellent correlation was obtained between "fast" MRI measurements and SM in MRI (SM vs BPMR interclass correlation coefficient ICC=0.965 and SM vs ALMR, ICC=0.958; P<0.05) with low interobserver variability (ICC=0.983 for SM; ICC=0.949 for BPMR; ICC=0.931 for ALMR). "Fast" measurements by MRI showed stadistical correlation between them (CCI=0.910) (Figure). Correlation between Echo and MRI measures was only moderate. (BPRM vs BPe CCI=0,469 mean difference -30 ml; ALMR vs MDDe ICC=0,456 mean difference -24 mL). Conclusions: ‘fast’ LAV measures by MRI are comparable with the MRI GS and also between them. Echo values seem to underestimate compared to MRI, so its use may not be suitable.
- Published
- 2014
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41. Poster session 4: Friday 5 December 2014, 08:30-12:30 * Location: Poster area
- Author
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Vascular, University, Semmelweis, Budapest, Hungary, and Group, MTA-SE Lendület Cardiovascular Imaging Research
- Abstract
Purpose: Although delayed-enhancement magnetic resonance imaging (DEMRI) is essential for diagnosis of cardiac sarcoidosis (CS), the test was not available when pacemaker was implamted. Recently, MR-conditional pacemaker has become avilable and we hypothesized that this device would be useful for diagnosis and management of CS. The aim of this study was to assess the diagnostic ability of MR-conditional pacemaker about CS in patients with advanced A-V nodal block (AAVB). Methods: Twenty-seven AAVB patients (14 men, 13 women; mean age, 69 ± 11 years) who were implanted MR-conditional pacemaker were studied. DEMRI was performed 6 weeks after implantation of permanent pacemaker. In patients with positive for DE, additional examinations like echocardiography, radioisotope imaging, biopsy, and coronary computed-tomography were performed due to confirm the diagnosis of CS and exclude coronary artery disease. Results: DE was observed in 12 patients (44 %). Out of 12 patients, 2 patients were excluded for having prior myocardial infarction. Seven of 10 (70 %) patients were diagnosed of CS by the consensus criteria. Compared with non-CS group, CS group had significantly lower age (61 ± 12 years vs. 72 ± 9 years p = 0.017). There was no significant difference about sex, angiotensin-converting enzyme, brain natriuretic peptide, and left ventricular ejection fraction between 2 groups. Six patients had started corticosteroid therapy and 5 patients (83%) recovered A-V nodal conduction. Conclusion: MR-conditional pacemaker was useful for diagnosis and management of patients with AAVB caused by CS.
Figure Cardiac MRI in patient with AV block - Published
- 2014
- Full Text
- View/download PDF
42. Reverse mortgage and risk profile awareness: Proposals for securitization
- Author
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Emilia Di Lorenzo, Gabriella Piscopo, Marilena Sibillo, Roberto Tizzano, Di Lorenzo, E., Piscopo, G., Sibillo, M., and Tizzano, R.
- Subjects
aging population ,real estate market ,securitization ,reverse mortgage ,Modeling and Simulation ,crossover risk ,Management Science and Operations Research ,aging population, crossover risk, real estate market, reverse mortgage, securitization ,General Business, Management and Accounting - Abstract
Reverse mortgages (RMs) are acquiring a growing centrality to meet the needs of a progressive aging population and to support the fragility of traditional pension systems. With an RM, an elderly individual gets a lump sum or a series of recur- ring payments whose amounts depend upon the expected liquidation value of his property and his age; he continues living in it until he dies, when the asset is sold and the proceeds are used to pay back the loan. The risk of these contracts, due to volatility of interest rates, house prices, and mortality rates, requires care- ful management strategies. This article analyzes the risk profile of the contract and suggests a securitization procedure where the lender averts the risks of the contract by engaging into an insurance contract through a special purpose vehicle that will issue ad-hoc bonds, whose underlying is determined by the lender’s gain/loss on the contract.
- Published
- 2022
43. Insurance incentives to pursue social well-being
- Author
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V. D’Amato, E. Di Lorenzo, G. Piscopo, M. Sibillo, Christos H. Skiadas, Charilaos Skiadas, D'Amato, V., Di Lorenzo, E., Piscopo, G., Sibillo, M., K. Skiadas, D’Amato, V., and C. H. Skiadas
- Subjects
Social wellbeing ,Insurance ,Health ,Sustainable Insurance ,Insurance Pandemic risk Securitization Social well-being Sustainability ,Securitized bond ,Social well-being ,Secutirization ,Insurance, Pandemic Risk, Securitization, Social well-being, Sustainability - Abstract
Current crisis, causing structural long-term changes in the economy and society, is offering a challenge to the insurance sector, whose primary role lies in the protection of individuals and productive activities. The insurance industry can take this opportunity towards achieving the objective of social well-being with the design of new insurance products and incentives. In this work we propose a particular type of securitization scheme where the health risk in a broad sense is transferred to capital market. For example, this tool can be exploited by firms to cover the risks of damage to the health of workers and office workers. Certain discount policies by insurance companies may encourage activities aimed at improving the health system and the work safety. An appropriate morbidity index is used to price this type of policy. Numerical results are offered and discussed.
- Published
- 2022
44. The Pricing of Reverse Mortgages in the Chinese Market
- Author
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Di Lorenzo Emilia, Sibillo Marilena, Piscopo Gabriella, Di Lorenzo, E., Piscopo, G., and Sibillo, M.
- Subjects
longevity risk, financial risk, reverse mortgages, pension product ,Longevity risk ,financial risk ,Applied Mathematics ,Financial risk ,longevity risk ,Chinese market ,reverse mortgages ,Business ,Monetary economics ,pension product - Abstract
Reverse mortgages (RM) are an attractive tool to increase retirement incomes and to face the needs of health care for elderly people. The investor in the RM market faces several risks: longevity risk, as retirees’ life expectancy increases, interest rate risk, especially in the low-rate post-crisis period, property market risk, in the last stage of the current business cycle. In our pricing model we incorporate the overall risk of the RM, focusing on the feature of the developing Chinese market.
- Published
- 2021
45. Risk Assessment in the Reverse Mortgage Contract
- Author
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E. Di Lorenzo, G. Piscopo, M. Sibillo, R. Tizzano, Corazza M., Gilli M., Perna C., Pizzi C., Sibillo M., Di Lorenzo, E., Piscopo, G., Sibillo, M., and Tizzano, R.
- Subjects
Reverse mortgage ,Personal pension products · Real estate · Reverse mortgage ,Personal pension product ,Real estate - Abstract
Changes in demographic structure of a country and economic condition are interconnected causes of new needs that motivate the launch of new financial instruments. One of these is the Reverse Mortgage (RM): a contract in which a homeowner borrows a part or the totality of the future liquidation value of his/her home at the time of his/her death. The paper analyses the contractual details and discusses the impact of the main variables on the lamp sum that an elderly homeowner receives at the inception of the contract. The risks factors that influence the pricing of the RM are both strictly demographic, i.e. the life of the contractor, and financial, in particular the evolution of the real estate market and of the financial market.
- Published
- 2021
46. Reverse mortgages through artificial intelligence: new opportunities for the actuaries
- Author
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Emilia Di Lorenzo, Gabriella Piscopo, R. Tizzano, Marilena Sibillo, Di Lorenzo, E., Piscopo, G., Sibillo, M., and Tizzano, R.
- Subjects
Pension Product ,Actuarial science ,Artificial intelligence · Neural network · Pension product · Real estate · Reverse mortgage ,Longevity risk ,Artificial Intelligence, Neural Network, Pension Product, Real Estate, Reverse Mortgage ,Reverse mortgage ,Neural Network ,Real estate ,Real Estate ,Liquidation value ,Interest rate risk ,Artificial Intelligence ,Dynamic pricing ,Market data ,Reverse Mortgage ,Business ,General Economics, Econometrics and Finance ,Finance ,Valuation (finance) - Abstract
In its basic structure, the reverse mortgage (RM) is a contract where a home owner borrows a part or the totality of the future liquidation value of his home at the time of his death. The risks that are borne by the lender are linked to the volatility of the real estate market, that is the house price risk, the financial market risk, that is the interest rate risk, and the uncertainty of the borrower’s lifetime, that is the longevity risk. The quantification of the future liquidation value and its valuation at the issue time is fundamental in the construction of the RM contract either in the perspective of the lender or in the one of the borrower. In the paper, we explore the use of neural networks to project the real estate market data; this approach allows to obtain a predictive analysis of the pricing process and indeed provides a dynamic pricing algorithm.
- Published
- 2020
47. P616Cardioprotective effects of nanoemulsions loaded with natural anti-inflammatory molecules against doxorubicin-induced cardiotoxicity in cardiomyocytes
- Author
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C Di Cicco, Paolo A. Netti, Giovanna Piscopo, C. Coppola, Nicola Maurea, Rosario Vincenz Iaffaioli, Rolando Paciello, Gerardo Botti, A. De Capua, Vincenzo Quagliariello, Raffaele Vecchione, Luscher TF, Maurea, N, Quagliariello, V, Vecchione, R, Di Cicco, C, De Capua, A, Coppola, C, Piscopo, G, Paciello, R, Iaffaioli, Rv, Netti, Pa, and Botti, G
- Subjects
Cardiotoxicity ,medicine.drug_class ,business.industry ,medicine ,Doxorubicin ,Pharmacology ,Cardiology and Cardiovascular Medicine ,business ,Anti-inflammatory ,medicine.drug - Abstract
Cardiotoxicity is one of the most significant adverse effects of the oncologic treatment with doxorubicin, which is responsible for a substantial morbid and mortality. Small molecules derived from medicinal plants with anti-inflammatory properties could have cardioprotective activites so potentially used in cardio-oncology management. Nanomedicine offer a new pharmacological tool able to increase bioavailability and protect natural bioactives with antiinflammatory and cardioprotective action.
- Published
- 2018
48. Trastuzumab and target-therapy side effects: Is still valid to differentiate anthracycline Type I from Type II cardiomyopathies?
- Author
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Giovanna Piscopo, Immacolata Capasso, Nicola Maurea, Claudia De Lorenzo, Emanuela Esposito, Carlo Maurea, Gennaro Riccio, C. Coppola, Riccio, Gennaro, Coppola, C, Piscopo, G, Capasso, I, Maurea, C, Esposito, E, DE LORENZO, Claudia, and Maurea, N.
- Subjects
Cardiac function curve ,Oncology ,medicine.medical_specialty ,Anthracycline ,medicine.medical_treatment ,Immunology ,Cardiomyopathy ,cardiotoxicity ,Antineoplastic Agents ,Breast Neoplasms ,030204 cardiovascular system & hematology ,Pharmacology ,anthracycline ,03 medical and health sciences ,0302 clinical medicine ,Trastuzumab ,Internal medicine ,medicine ,Immunology and Allergy ,Humans ,Retrospective Studies ,anthracyclines ,Heart Failure ,Cardiotoxicity ,Clinical Trials as Topic ,business.industry ,Cancer ,Immunotherapy ,medicine.disease ,trastuzumab ,030220 oncology & carcinogenesis ,Heart failure ,Commentary ,cancer therapy ,Female ,immunotherapy ,business ,Cardiomyopathies ,medicine.drug - Abstract
The improvement in cancer therapy and the increasing number of long term survivors unearth the issue of cardiovascular side effects of anticancer treatments. As a paradox in cancer survivors, delayed cardiotoxicity has emerged as a significant problem. Two categories of cardiotoxic side effects of antineoplastic drugs have been previously proposed: Type I cardiotoxicity, defined as permanent cardiotoxicity, is usually caused by anthracyclines; Type II cardiotoxicity, considered as reversible cardiotoxicity, has been mainly related to monoclonal antibodies. The cardiotoxicity of antibodies has been associated to trastuzumab, a humanized anti-ErbB2 monoclonal antibody currently in clinical use for the therapy of breast carcinomas, which induces cardiac dysfunction when used in monotherapy, or in combination with anthracyclines. Furthermore, recent retrospective studies have shown an increased incidence of heart failure and/or cardiomyopathy in patients treated with trastuzumab, that can persist many years after the conclusion of the therapy, thus suggesting that the side toxic effects are not always reversible as it was initially proposed. On the other hand, early detection and prompt therapy of anthracycline associated cardiotoxicity can lead to substantial recovery of cardiac function. On the basis of these observations, we propose to find a new different classification for cardiotoxic side effects of drugs used in cancer therapy.
- Published
- 2016
49. RANOLAZINE AT THE END OF TRASTUZUMAB THERAPY PREVENTS LEFT VENTRICULAR DYSFUNCTION: IN VITRO AND IN VIVO STUDY
- Author
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Giovanna Piscopo, Gennaro Riccio, Nicola Maurea, Claudia De Lorenzo, Domenica Rea, Claudio Arra, Carmela Coppola, Gerolama Condorelli, Maurea, N, Coppola, C, Piscopo, G, Rea, D, Riccio, Gennaro, Condorelli, Gerolama, Arra, C, and DE LORENZO, Claudia
- Subjects
medicine.medical_specialty ,business.industry ,Trastuzumab ,In vivo ,Internal medicine ,Cardiology ,Medicine ,Ranolazine ,Cardiology and Cardiovascular Medicine ,business ,In vitro ,medicine.drug - Published
- 2016
50. Urinary epidermal growth factor/monocyte chemotactic peptide 1 ratio as non-invasive predictor of Mayo clinic imaging classes in autosomal dominant polycystic kidney disease.
- Author
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Rocchetti MT, Pesce F, Matino S, Piscopo G, di Bari I, Trepiccione F, Capolongo G, Perniola MA, Song X, Khowaja S, Haghighi A, Peters D, Paolicelli S, Pontrelli P, Netti GS, Ranieri E, Capasso G, Moschetta M, Pei Y, and Gesualdo L
- Subjects
- Animals, Humans, Mice, Disease Progression, Epidermal Growth Factor genetics, Kidney, Monocytes pathology, Polycystic Kidney, Autosomal Dominant diagnostic imaging, Polycystic Kidney, Autosomal Dominant genetics
- Abstract
Background: Age- and height-adjusted total kidney volume is currently considered the best prognosticator in patients with autosomal dominant polycystic kidney disease. We tested the ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 for the prediction of the Mayo Clinic Imaging Classes., Methods: Urinary epidermal growth factor and monocyte chemotactic peptide 1 levels were measured in two independent cohorts (discovery, n = 74 and validation set, n = 177) and healthy controls (n = 59) by immunological assay. Magnetic resonance imaging parameters were used for total kidney volume calculation and the Mayo Clinic Imaging Classification defined slow (1A-1B) and fast progressors (1C-1E). Microarray and quantitative gene expression analysis were used to test epidermal growth factor and monocyte chemotactic peptide 1 gene expression., Results: Baseline ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 correlated with total kidney volume adjusted for height (r = - 0.6, p < 0.001), estimated glomerular filtration rate (r = 0.69 p < 0.001), discriminated between Mayo Clinic Imaging Classes (p < 0.001), and predicted the variation of estimated glomerular filtration rate at 10 years (r = - 0.51, p < 0.001). Conditional Inference Trees identified cut-off levels of the ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 for slow and fast progressors at > 132 (100% slow) and < 25.76 (89% and 86% fast, according to age), with 94% sensitivity and 66% specificity (p = 6.51E-16). Further, the ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 at baseline showed a positive correlation (p = 0.006, r = 0.36) with renal outcome (delta-estimated glomerular filtration rate per year, over a mean follow-up of 4.2 ± 1.2 years). Changes in the urinary epidermal growth factor and monocyte chemotactic peptide 1 were mirrored by gene expression levels in both human kidney cysts (epidermal growth factor: - 5.6-fold, fdr = 0.001; monocyte chemotactic peptide 1: 3.1-fold, fdr = 0.03) and Pkd1 knock-out mouse kidney (Egf: - 14.8-fold, fdr = 2.37E-20, Mcp1: 2.8-fold, fdr = 6.82E-15)., Conclusion: The ratio of urinary epidermal growth factor and monocyte chemotactic peptide 1 is a non-invasive pathophysiological biomarker that can be used for clinical risk stratification in autosomal dominant polycystic kidney disease., (© 2022. The Author(s).)
- Published
- 2023
- Full Text
- View/download PDF
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