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116 results on '"Previti M"'

1. Terrorism and War: Twitter Cascade Analysis

Author

Carchiolo, V., Longheu, A., Malgeri, M., Mangioni, G., Previti, M., Kacprzyk, Janusz, Series Editor, Del Ser, Javier, editor, Osaba, Eneko, editor, Bilbao, Miren Nekane, editor, Sanchez-Medina, Javier J., editor, Vecchio, Massimo, editor, and Yang, Xin-She, editor

Published
2018
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4. A Trust-Based News Spreading Model

Author

Carchiolo, V., Longheu, A., Malgeri, M., Mangioni, G., Previti, M., Cornelius, Sean, editor, Coronges, Kate, editor, Gonçalves, Bruno, editor, Sinatra, Roberta, editor, and Vespignani, Alessandro, editor

Published
2018
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17. Continuosus subcutaneos glucose minitoring in diabetic patients: a multicenter analysis

Author

Maran A, Crepaldi C, Tiengo A, Grassi G, Vitali E, Pagano G, Bistoni S, Calabrese G, Santeusanio F, Leonetti F, Ribaudo M, Di Mario U, Previti M, Cucinotta D, Giorgino F, Bellomo A, Giorgino R, Poscia A, Varalli M., ANNUZZI, GIOVANNI, GENOVESE, SALVATORE, RICCARDI, GABRIELE, Maran, A, Crepaldi, C, Tiengo, A, Grassi, G, Vitali, E, Pagano, G, Bistoni, S, Calabrese, G, Santeusanio, F, Leonetti, F, Ribaudo, M, Di Mario, U, Annuzzi, Giovanni, Genovese, Salvatore, Riccardi, Gabriele, Previti, M, Cucinotta, D, Giorgino, F, Bellomo, A, Giorgino, R, Poscia, A, and Varalli, M.

Published
2002

23. Identifying patients at risk for microalbuminuria via interaction of the components of the metabolic syndrome: a cross-sectional analytic study

Author

Gentile, L., Cichero, P., Di Berardino, P., Di Petta, C., Montani, V., Poli, M., Grosso, J., De Marco, F., Perticone, F., Mattace, A., Vatrano, M., Ventura, G., Sprovieri, M., Spagnuolo, V., Mastropasqua, A., Marenco, P., Caruso, M., D’Ugo, E., Squadrone, M. R., Pupillo, M., Minnucci, A., De Luca, A., Tagliaferri, M., Vitale, C., Sciangula, L., Banfi, E., Cucinotta, D., Dibenedetto, A., Previti, M., Tiengo, A., Avogaro, A., Bettio, M., Dekreuzenberg, S., Galluzzo, A., Camilleri, C., Merlino, S., Sinagra, D., Provenzano, V., Fleres, M., Carnovali, M., Crespi, E., Sommariva, M., Vecchio, C., Consoli, A., Ciccarone, E., Devangelio, E., Formoso, G., Taraborrelli, M., Seghieri, G., Alviggi, L., Bardini, G., De Bellis, A., Porro, T., Bianchi, A., Dagani, R., Di Battista, R., Ferrario, A., Ottaviano, R., Gambardella, S., Bracaglia, D., Testa, G., Mancini, A., Giannini, D., Monesi, G., Mollo, F., Osti, M., Di Michele, D., Lattanzi, E., Piersanti, C., Ghigo, E., Camanni, F., Destefanis, S., Gaia, D., Gasco, V., Maccario, M., Carretta, R., Fiammengo, F., Gerloni, R., Macaluso, L., Donnini, P., Alvaro, S., Ambrosio, G. B., Leprotti, C., Moro, E., Pais, M., Pianetti, S., Garbin, A., Frascone, V., Marmo, P., Munari, G. F., Cataldi, B., Filiani, M. L., Ursini, G., Augello, M., Tassan, P., Giraldi, D., Berarducci, G., Braggion, M., Novelletto, B. F., Dell’Orco, R. L., Baj, A., Pardo, S., Persia, M., Bellini, F., Nistico, F., Rossi, C. L., Quinzii, G., Ferrigato, A., Zaramella, M. L., Crisante, E., Biundo, G., Serughetti, G., Sofra, D., Trono, L., Arduino, G., Chiappetta, S., Novarese, I., Monari, M., Cappello, I., Lipari, L., Bersani, G. P., Marcomini, G., Felici, M. G., Bragiotto, A., Felice, L., Caberletti, I., Vergani, P., Orecchia, E., Ferracin, F., Cavallo, G., Giardina, L., Felloni, L., Cesarone, L., Albanese, V., Bizzozero, L., Cerati, C., Mauri, L., Ratti, C., Alecci, U., Alibrando, A., Forastiere, G., Petrella, G., Di Mattia, Q., Grimaldi, N., Olivieri, I., Cardella, M. C., Duren, B., Falzone, A., Furlan, G., Nesladek, N., Novel, N., Pasquariello, M., Russo, M., Veglia, D., Fusello, M., Baldi, C., Seller, R., Tosi, G., Barberio, S., Tonon, R., Cardinale, G., Lombardo, F. P., Magliozzo, F., Merlino, G., Merlino, N., Quartetti, G., Bolognese, F., Baglieri, S., Giarrusso, P., Speciale, S., Buffone, M., Di Domizio, O., Panzieri, F., Perfetto, G., Granati, A., Lattari, P. R., Potenti, P. G., Quattrocchi, M., Vannucci, R., Daddi, L., Dallatorre, G., Guido, G. P., Orlando, F., Santoro, A., Zagni, R., Genova, O., Alaimo, A., Canfora, M., Cappelli, C., Caracciolo, F., Casimirri, R., Crestini, A. M., Daniele, G., De Lucia, L., Demarchis, A., Di Masi, A., Di Rosa, F., Filabozzi, A., Levati, M., Lucente, A., Manzo, G., Marchionne, M., Marino, G. A., Paolini, E., Quaresima, M., Scala, P., Scotto, M., Scotto, R., Simeoni, A., Chieregato, G., Sparesato, S., Cavallo, E., Ceglia, G., Chiarini, T., Visentini, E., Sammarone, R., Di Giambattista, P., Fumagalli, M. A., Milanese, F., Santoro, L., Giusti, P., Nafra, G., Romito, G., Balsamo, R., Rinaldi, M., Biondo, F., Consiglio, G., Arbore, G., Garione, I., Merlini, C., Pizzini, A., Titta, G., Vitali, S., Rotondo, G., Berardi, A., Castellani, G., Cova, L. V., Lamberti, C., Granzotto, S., Mazzi, P. A., Bergamasco, G., Autiero, V., and L. Ghiraldelli.

Subjects
Male, medicine.medical_specialty, Multivariate analysis, endocrine system diseases, Epidemiology, Population, urologic and male genital diseases, Critical Care and Intensive Care Medicine, Impaired glucose tolerance, Insulin resistance, Risk Factors, Diabetes mellitus, Internal medicine, medicine, Albuminuria, Humans, education, Aged, Metabolic Syndrome, Transplantation, education.field_of_study, business.industry, nutritional and metabolic diseases, Middle Aged, medicine.disease, female genital diseases and pregnancy complications, Endocrinology, Cross-Sectional Studies, Nephrology, Homogeneous, Microalbuminuria, Female, Metabolic syndrome, business
Abstract

The objective of this study was to investigate correlates of risk for having microalbuminuria in individuals with one or more cardiovascular risk factors.The study involved 1919 individuals who attended general practice settings, were aged 55 to 75 yr, and did not have a history of cardiovascular events or diabetes but had one or more cardiovascular risk factors. A tree-based regression technique and multivariate analysis were used to identify distinct, homogeneous subgroups of patients with different likelihood of having microalbuminuria; interaction between correlates of microalbuminuria and risk for microalbuminuria was also investigated.The prevalence of microalbuminuria was 5.9%. Patients who did not have hypertension and had postload glycemia140 mg/dl showed the lowest prevalence of microalbuminuria (1.9%) and represented the reference class. The likelihood of microalbuminuria was seven times higher in men with hypertension and homeostatic model assessment levels in the upper tertile and four times higher in women with the same characteristics. Individuals with hypertension and lower homeostatic model assessment levels and normotensive individuals with postload glycemiaor = 140 mg/dl had a more than three-fold increased likelihood of having microalbuminuria. Treatment with statins was associated with a 54% reduction in the likelihood of having microalbuminuria, whereas levels of triglycerides150 mg/dl and fibrinogen levels in the upper tertile were associated with a significantly higher risk for microalbuminuria.The likelihood of having microalbuminuria in a population-based study of elderly individuals is strongly related to the interaction between the components of the metabolic syndrome, particularly hypertension, insulin resistance, and impaired glucose tolerance.

Published
2007

25. Use of the Diabetes Risk Score for Opportunistic Screening of Undiagnosed Diabetes and Impaired Glucose Tolerance: The IGLOO (Impaired Glucose Tolerance and Long-Term Outcomes Observational) study

Author

Muggeo, M., Caimi, V., Capani, F., Cucinotta, D., Grimaldi, N., Montanari, P., Mocarelli, P., Signorini, S., Dinardo, B., Ferrari, S., Piaggione, M., Gentile, L., Cichero, P., Di Berardino, P., Di Petta, C., Montani, V., Poli, M., Grosso, J., De Marco, F., Perticone, F., Mattace, A., Vatrano, M., Ventura, G., Sprovieri, M., Spagnuolo, V., Mastropasqua, A., Marenco, P., D’Ugo, E., Squadrone, M. R., Pupillo, M., De Luca, A., Mennucci, A., Tagliaferri, M., Vitale, C., Sciangula, L., Banfi, E., Di Benedetto, A., Previti, M., Tiengo, A., Avogaro, A., Bettio, De Kreuzenberg, S., Galluzzo, A., Camilleri, C., Merlino, S., Sinagra, D., Provenzano, V., Fleres, M., Spano, L., Carnovali, M., Crespi, E., Sommariva, M., Vecchio, C., Consoli, A., Ciccarone, E., Devangelio, E., Formoso, G., Seghieri, G., Alviggi, L., Bardini, G., De Bellis, A., Porro, T., Bianchi, A., Dagani, R., Di Battista, R., Ferrario, Gambardella, S., Bracaglia, D., Testa, G., Giannini, D., Mancini, A., Monesi, G., Mollo, F., Osti, M., Di Michele, D., Lattanzi, E., Piersanti, C., Ghigo, E., Camanni, F., Destefanis, S., Gaia, D., Gasco, V., Maccario, M., Carretta, R., Fiammengo, F., Gerloni, R., Macaluso, L., Donnini, P., Alvaro, S., Ambrosio, G. B., Leprotti, C., Moro, E., Pais, M., Pianetti, S., Garbin, A., Frascone, V., Marmo, P., Munari, G. F., Cataldi, B., Ursini, G., Augello, M., Braggion, M., Baj, A., Persia, M., Nistico’, F., Rossi, C. L., Quinzii, G., Ferrigato, A., Zaramella, M. L., Serughetti, G., Sofra, D., Arduino, G., Chiappetta, S., Novarese, I., Monari, M., Cappello, I., Lipari, L., Marcomini, G., Felice, L., Caberletti, I., Vergani, P., Orecchia, E., Ferracin, F., Cavallo, G., Giardina, L., Felloni, L., Cesarone, L., Bizzozero, L., Ratti, C., Alecci, U., Marino, S., Forastiere, G., Petrella, G., Olivieri, I., Cardella, M. C., Duren, B., Furlan, G., Novel, N., Pasquariello, M., Russo, M., Baldi, C., Seller, R., Tosi, G., Barberio, S., Cardinale, G., Lombardo, F. P., Magliozzo, F., Merlino, G., Merlino, N., Quartetti, G., Bolognese, F., Baglieri, S., Speciale, S., Buffone, M., Di Domizio, O., Panzieri, F., Perfetto, G., Potenti, P. G., Quattrocchi, M., Vannucci, R., Daddi, L., Guido, G. P., Orlando, F., Santoro, A., Zagni, R., Canfora, M., Cappelli, C., Caracciolo, F., Casimirri, R., Crestini, A. M., De Marchis, A., Di Masi, A., Lucente, A., Manzo, G., Marchionne, M., Marino, G. A., Paolini, E., Scala, P., Scotto, M., Scotto, R., Simeoni, A., Chieregato, G., Cavallo, E., Ceglia, G., Chiarini, T., Visentini, E., Sammarone, R., Fumagalli, M. A., Milanese, F., Giusti, P., Balsamo, R., Rinaldi, M., Biondo, F., Consiglio, G., Garione, I., Merlini, C., Pizzini, A., Titta, G., Vitali, S., Rotondo, G., Cova, L. V., Lamberti, C., Granzotto, S., Mazzi, P. A., and Ghiraldelli, L.

Published
2005

29. High prevalence of non-organ-specific autoantibodies in hepatitis C virus-infected cirrhotic patients from southern Italy

Author

Squadrito, Giovanni, Previti, M., Lenzi, M., Le Rose, E. P., Caccamo, Gaia, Restuccia, T., Cesare, E. D., Pollicino, Teresa, and Raimondo, Giovanni

Subjects
Liver Cirrhosis, Adult, Male, Biopsy, Adult, Age Distribution, Aged, Autoantibodies, Biopsy, Needle, Case-Control Studies, Cohort Studies, Female, Hepatitis C Antibodies, Hepatitis C, Chronic, Humans, Italy, Liver Cirrhosis, Biliary, Male, Middle Aged, Prevalence, Probability, Reference Values, Risk Assessment, Seroepidemiologic Studies, Severity of Illness Index, Sex Distribution, Risk Assessment, Severity of Illness Index, Cohort Studies, Age Distribution, Reference Values, Seroepidemiologic Studies, Needle, Prevalence, Humans, Chronic, Sex Distribution, Aged, Autoantibodies, Probability, Liver Cirrhosis, Biliary, Biliary, Biopsy, Needle, Hepatitis C Antibodies, Hepatitis C, Chronic, Middle Aged, Hepatitis C, Italy, Case-Control Studies, Female
Abstract

Non-organ-specific autoantibodies (NOSAs) are frequently found in patients with hepatitis C virus (HCV) chronic infection. Genetics is likely involved in the development of autoimmune reactivities, and differences in the prevalence of HCV-related autoantibodies among populations of various geographic areas should be expected. We evaluated the prevalence and the clinical impact of NOSAs in a series of HCV-infected patients from southern Italy. We studied 283 consecutive anti-HCV positive patients (162 men, 121 women, mean age 54.5 +/- 13.5 years), 94 of whom were cirrhotics and 189 noncirrhotics. Serum from each patient and from 41 hepatitis B surface antigen (HBsAg)-positive/anti-HCV negative control subjects were tested (dilution 1:40) for autoantibodies by indirect immunofluorescence. Qualitative/quantitative HCV-RNA determinations were also performed. The prevalence of NOSAs was significantly higher in anti-HCV-positive subjects than in HBsAg-positive patients (P0.006). Autoantibodies were significantly associated with both cirrhosis (P0.0001) and older age (P0.05). No significant association between NOSAs and either female gender or virological parameters (HCV-RNA positivity, viral load, and genotype) was found. In conclusion, the autoantibody positivity in HCV-infected patients from southern Italy is significantly related to cirrhosis and older age, although its general prevalence is similar to that reported in populations from the north of the country.

Published
2003

32. Continuous subcutaneous glucose monitoring in diabetic patients: a multicenter analysis

Author

Maran, Alberto, Crepaldi, C, Tiengo, Antonio, Grassi, G, Vitali, E, Pagano, G, Bistoni, S, Calabrese, G, Santeusanio, F, Leonetti, F, Ribaudo, M, DI MARIO, U, Annuzzi, G, Genovese, S, Riccardi, G, Previti, M, Cucinotta, D, Giorgino, F, Bellomo, A, Giorgino, R, Poscia, A, and Varalli, M.

Subjects
Adult, Male, Diabetes Mellitus, Type 1, Glucose, Diabetes Mellitus, Type 2, Microdialysis, Humans, Reproducibility of Results, Female, Middle Aged, Monitoring, Physiologic, Skin
Abstract

To evaluate the accuracy of a new subcutaneous glucose sensor (Glucoday; A. Menarini Diagnostics) compared with venous blood glucose measurement in type 1 and type 2 diabetic patients.A multicenter study was performed in 70 diabetic patients. A microdialysis fiber was inserted subcutaneously into the periumbelical region and perfused with a buffer solution. Glucose concentrations in the dialysate were then measured every 3 min by the glucose sensor over a 24-h period, during which nine venous blood samples were also collected throughout the day.Both the insertion of the fiber and the wearing of the device were well tolerated by the patients. Subcutaneous glucose levels were well correlated with venous glucose measurements (r = 0.9, P0.001) over a wide range (40-400 mg/dl) for up to 24 h, with a single-point calibration. An analysis of 381 data pairs showed a linear relationship between the GlucoDay and serial venous blood glucose levels, and 97% of the data fell in the A and B regions of the error grid analysis. Percentage bias between the GlucoDay and the blood venous levels was -2.0% in the hypoglycemic range (70 mg/dl), 6.9% in the euglycemic range (70-180 mg/dl), and 11.2% in the hyperglycemic range (180 mg/dl).The GlucoDay system demonstrated high reliability and reported values that closely agreed with venous blood glucose measurements. The system was well tolerated and thus constitutes a relatively easy method to monitor glucose excursions in diabetic patients.

Published
2002

47. Continuous subcutaneous glucose monitoring in diabetic patients: A multicenter evaluation

Author

Maran, A, primary, Crepaldi, C, additional, Tiengo, A, additional, Grassi, G, additional, Vitali, E, additional, Pagano, G, additional, Bistoni, S, additional, Calabrese, G, additional, Santeusanio, F, additional, Leonetti, F, additional, Ribaudo, M, additional, Di Mario, U, additional, Annuzzi, G, additional, Genovese, S, additional, Riccardi, G, additional, Previti, M, additional, Cucinotta, D, additional, Giorgino, F, additional, Perrini, S, additional, Giorgino, R, additional, Poscia, A, additional, and Varalli, M, additional

Published
2000
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50. Gastric mucosal mast cells in atopic subjects

Author

Bagnato, G. F., primary, Cesare, E., additional, Caruso, R. A., additional, Gulli, S., additional, Cugliari, A., additional, Morabito Lo Prete, A., additional, Previti, M., additional, Muscarà, M., additional, and Bottari, M., additional

Published
1995
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