Changes in cervical cancer incidence following the introduction of organized screening in Italy von Serraino, Diego, Gini, Andrea, Taborelli, Martina, Ronco, Guglielmo, Giorgi-Rossi, Paolo, Zappa, Marco, Crocetti, Emanuele, Franzo, Antonella, Falcini, Fabio, Visioli, Carmen Beatriz, Stracci, Fabrizio, Zorzi, Manuel, Federico, Massimo, Michiara, Maria, Fusco, Mario, Ferretti, Stefano, Pannozzo, Fabio, Tisano, Francesco, Zanetti, Roberto, Zucchetto, Antonella

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Screening patterns within organized programs and survival of Italian women with invasive cervical cancer von Zucchetto, Antonella, Ronco, Guglielmo, Giorgi Rossi, Paolo, Zappa, Marco, Ferretti, Stefano, Franzo, Antonella, Falcini, Fabio, Visioli, Carmen Beatriz, Zanetti, Roberto, Biavati, Patrizia, La Rosa, Francesco, Baracco, Susanna, Federico, Massimo, Campari, Cinzia, De Togni, Aldo, Piffer, Silvano, Pannozzo, Fabio, Fusco, Mario, Michiara, Maria, Castaing, Marine, Seghini, Pietro, Tisano, Francesco, Serraino, Diego

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Cervical cancer screening in the Ferrara Local Health Authority catchment area von Bergamini, M, Buriani, O, Cucchi, A, De Togni, A, Carpanelli, M C, Cervato, K, Gigli, F, Pizzo, F, Ravasini, G, Rauli, G, Rizzello, R, Gregorio, P

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A Microchip Integrated Sensor for the Monitoring of High Concentration Photo-voltaic Solar Modules von Corte, F.G. Della, Cocorullo, G., Corsonello, P., Felini, C., Merenda, M., Perri, S., Borelli, G., Carpanelli, M., Verdilio, D.

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A REference implementation of interoperable indoor location & communication systems for First REsponders: The REFIRE project von Pascucci, F., Panzieri, S., Setola, R., Oliva, G., Marsella, S., Marzoli, M., Delprato, U., Borelli, G., Carpanelli, M.

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Bilateral preaxial polydactyly in a WAGR syndrome patient von Manoukian, Siranoush, Crolla, John A., Mammoliti, Palma M.A., Testi, Maria Adele, Zanini, Rinaldo, Carpanelli, Maria Luisa, Piozzi, Elena, Sozzi, Gabriella, De Vecchi, Giovanna, Terenziani, Monica, Spreafico, Filippo, Collini, Paola, Radice, Paolo, Perotti, Daniela

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, GI, Kitabayashi, N, Barth, M, Briggs, TA, Burton, ACE, Carpanelli, ML, Cerisola, AM, Colson, C, Dale, RC, Danti, FR, Darin, N, De Azua, B, De Giorgis, V, De Goede, CGL, Desguerre, I, De laet, C, Eslahi, A, Fahey, MC, Fallon, P, Fay, A, Fazzi, E, Gorman, MP, Gowrinathan, NR, Hully, M, Kurian, MA, Leboucq, N, Lin, J-PS-M, Lines, MA, Mar, SS, Maroofian, R, Marti-Sanchez, L, McCullagh, G, Mojarrad, M, Narayanan, V, Orcesi, S, Ortigoza-Escobar, JD, Perez-Duenas, B, Petit, F, Ramsey, KM, Rasmussen, M, Rivier, F, Rodriguez-Pombo, P, Roubertie, A, Stodberg, TI, Toosi, MB, Toutain, A, Uettwiller, F, Ulrick, N, Vanderver, A, Waldman, A, Livingston, JH, Crow, YJ

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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 von Crow, Yanick J., Chase, Diana S., Lowenstein Schmidt, Johanna, Szynkiewicz, Marcin, Forte, Gabriella M.A., Gornall, Hannah L., Oojageer, Anthony, Anderson, Beverley, Helman, Guy, Abdel-Salam, Ghada M., Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon-Shalev, Stavit, Arellano, Montse, Ariaudo, Giada, Aswani, Vijay, Babul-Hirji, Riyana, Bahi-Buisson, Nadia, Bailey, Kathryn M., Barth, Magalie, Battini, Roberta, Beresford, Michael W., Bernard, Geneviève, Bianchi, Marika, Blair, Edward M., Burlina, Alberto B., Luisa Carpanelli, Maria, Castro-Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E., Chitayat, David A., Collins, Abigail E., Sierra Corcoles, Concepcion, Cordeiro, Nuno J.V., Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C., De Goede, Christian G.E.L., De Laet, Corinne, De Waele, Liesbeth M.H., Desguerre, Isabelle, Devriendt, Koenraad, Fazzi, Elisa, Figueiredo, António, Gener, Blanca, Goizet, Cyril, Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Khan, Nasaim, King, Mary D., Kumar, Ram, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, Lim, Ming J., Lin, Jean-Pierre S.-M., Linnankivi, Tarja, Mackay, Mark T., Marom, Daphna R., McKee, Shane A., Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez-Enamorado, Noemi, Oades, Patrick J., Ostergaard, John R., Pérez-Dueñas, Belén, Prendiville, Julie S., Rasmussen, Magnhild, Ricci, Federica, Rio, Marlène, Rodriguez, Diana, Roubertie, Agathe, Sinha, Gyanranjan P., Soler, Doriette, Spiegel, Ronen, Stödberg, Tommy I., Straussberg, Rachel, Suri, Mohnish, Tan, Tiong Y., te Water Naude, Johann, Maria Valente, Enza, van der Knaap, Marjo S., Vassallo, Grace, Vijzelaar, Raymon, Wallace, Geoffrey B., Wassmer, Evangeline, Webb, Hannah J., Whitehouse, William P., Whitney, Robyn N., Zaki, Maha S., Zuberi, Sameer M., Livingston, John H., Rozenberg, Flore, Vanderver, Adeline, Orcesi, Simona, Rice, Gillian I.

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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature von Rice, Gillian I, Kasher, Paul R, Forte, Gabriella M A, Mannion, Niamh M, Greenwood, Sam M, Szynkiewicz, Marcin, Dickerson, Jonathan E, Bhaskar, Sanjeev S, Zampini, Massimiliano, Briggs, Tracy A, Jenkinson, Emma M, Bacino, Carlos A, Battini, Roberta, Bertini, Enrico, Brogan, Paul A, Brueton, Louise A, Carpanelli, Marialuisa, De Laet, Corinne, de Lonlay, Pascale, del Toro, Mireia, Desguerre, Isabelle, Fazzi, Elisa, Garcia-Cazorla, Àngels, Heiberg, Arvid, Kawaguchi, Masakazu, Kumar, Ram, Lin, Jean-Pierre S-M, Lourenco, Charles M, Male, Alison M, Marques, Wilson, Mignot, Cyril, Olivieri, Ivana, Orcesi, Simona, Prabhakar, Prab, Rasmussen, Magnhild, Robinson, Robert A, Rozenberg, Flore, Schmidt, Johanna L, Steindl, Katharina, Tan, Tiong Y, van der Merwe, William G, Vanderver, Adeline, Vassallo, Grace, Wakeling, Emma L, Wassmer, Evangeline, Whittaker, Elizabeth, Livingston, John H, Lebon, Pierre, Suzuki, Tamio, McLaughlin, Paul J, Keegan, Liam P, O'Connell, Mary A, Lovell, Simon C, Crow, Yanick J

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, GI, Kitabayashi, N, Barth, M, Briggs, TA, Burton, ACE, Carpanelli, ML, Cerisola, AM, Colson, C, Dale, RC, Danti, FR, Darin, N, De Azua, B, De Giorgis, V, De Goede, CGL, Desguerre, I, De Laet, C, Eslahi, A, Fahey, MC, Fallon, P, Fay, A, Fazzi, E, Gorman, MP, Gowrinathan, NR, Hully, M, Kurian, MA, Leboucq, N, Lin, JPSM, Lines, MA, Mar, SS, Maroofian, R, Marti-Sanchez, L, McCullagh, G, Mojarrad, M, Narayanan, V, Orcesi, S, Ortigoza-Escobar, JD, Perez-Duenas, B, Petit, F, Ramsey, KM, Rasmussen, M, Rivier, F, Rodriguez-Pombo, P, Roubertie, A, Stodberg, TI, Toosi, MB, Toutain, A, Uettwiller, F, Ulrick, N, Vanderver, A, Waldman, A, Livingston, JH, Crow, YJ

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Validation of healthcare administrative data for the diagnosis of epilepsy von Franchi, C, Giussani, G, Messina, P, Montesano, M, Romi, S, Nobili, A, Fortino, I, Bortolotti, A, Merlino, L, Beghi, E

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Characterization of the Ecosole HCPV tracker and single module inverter

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Tuning the assembling process of modules by the use of proper equipment von Herrero, Rebeca, Askins, Stephen, Antón, Ignacio, Sala, Gabriel, De Nardis, Davide, Borelli, Gianni, Carpanelli, Maurizio, Verdilio, Daniele

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Characterization and performance analysis of Ecosole HCPV system first prototype von Cancro, Carmine, Graditi, Giorgio, Ciniglio, Gabriele, Leanza, Gianni, Borriello, Aniello, Merola, Angelo, Ferlito, Sergio, Borelli, Gianni, Carpanelli, Maurizio, Verdilio, Daniele, De Nardis, Davide, Migali, Fabrizio

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Characterization and validation tests on Ecosole C-modules first prototypes

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, Gillian, Kitabayashi, Naoki, Barth, Magalie, Briggs, Tracy, Burton, Annabel C.E, Luisa Carpanelli, Maria, Cerisola, Alfredo M, Colson, Cindy, Dale, Russell C, Danti, Federica Rachele, Darin, Niklas, De Azua, Begoña, De Giorgis, Valentina, De Goede, Christian G E L, Desguerre, Isabelle, De Laet, Corinne, Eslahi, Atieh, Fahey, Michael C, Fallon, Penny, Fay, Alexander J, Fazzi, Elisa, Gorman, Mark P, Gowrinathan, Nirmala Rani, Hully, Marie, Kurian, Manju A, Leboucq, Nicolas, Lin, Jean-Pierre S-M, Lines, Matthew A, Mar, Soe S, Maroofian, Reza, Martí-Sanchez, Laura, McCullagh, Gary, Mojarrad, Majid, Narayanan, Vinodh, Orcesi, Simona, Ortigoza-Escobar, Juan Dario, Pérez-Dueñas, Belén, Petit, Florence, Ramsey, Keri M, Rasmussen, Magnhild, Rivier, François, Rodríguez-Pombo, Pilar, Roubertie, Agathe, Stödberg, Tommy I, Beiraghi Toosi, Mehran, Toutain, Annick, Uettwiller, Florence, Ulrick, Nicole, Vanderver, Adeline, Waldman, Amy, Livingston, John H, Crow, Yanick

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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 von Crow, Yanick J, Chase, Diana S, Lowenstein Schmidt, Johanna, Szynkiewicz, Marcin, Forte, Gabriella M.A, Gornall, Hannah L, Oojageer, Anthony, Anderson, Beverley, Pizzino, Amy, Helman, Guy, Abdel-Hamid, Mohamed S, Abdel-Salam, Ghada M, Ackroyd, Sam, Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon-Shalev, Stavit, Arellano, Montse, Ariaudo, Giada, Aswani, Vijay, Babul-Hirji, Riyana, Baildam, Eileen M, Bahi-Buisson, Nadia, Bailey, Kathryn M, Barnerias, Christine, Barth, Magalie, Battini, Roberta, Beresford, Michael W, Bernard, Geneviève, Bianchi, Marika, Billette de Villemeur, Thierry, Blair, Edward M, Bloom, Miriam, Burlina, Alberto B, Luisa Carpanelli, Maria, Carvalho, Daniel R, Castro-Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E, Chitayat, David A, Collins, Abigail E, Sierra Corcoles, Concepcion, Cordeiro, Nuno J.V, Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C, D Arrigo, Stefano, De Goede, Christian G.E.L, De Laet, Corinne, De Waele, Liesbeth, Denzler, Ines, Desguerre, Isabelle, Devriendt, Koenraad, Di Rocco, Maja, Fahey, Michael C, Fazzi, Elisa, Ferrie, Colin D, Figueiredo, António, Gener, Blanca, Goizet, Cyril, Gowrinathan, Nirmala R, Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Kara, Bülent, Khan, Nasaim, King, Mary D, Kirk, Edwin P, Kumar, Ram, Lagae, Lieven, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, Piana, Roberta La, Lim, Ming J, Lin, Jean-Pierre S.-M, Linnankivi, Tarja, Mackay, Mark T, Marom, Daphna R, Marques Lourenço, Charles, McKee, Shane A, Moroni, Isabella, Morton, Jenny E.V, Moutard, Marie-Laure, Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez-Enamorado, Noemi, Oades, Patrick J, Olivieri, Ivana, Ostergaard, John R, Pérez-Dueñas, Belén, Prendiville, Julie S, Ramesh, Venkateswaran, Rasmussen, Magnhild, Régal, Luc, Ricci, Federica, Rio, Marlène, Rodriguez, Diana

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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature von Rice, Gillian I, Kasher, Paul R, Forte, Gabriella M A, Mannion, Niamh M, Greenwood, Sam M, Szynkiewicz, Marcin, Dickerson, Jonathan E, Bhaskar, Sanjeev S, Zampini, Massimiliano, Briggs, Tracy A, Jenkinson, Emma M, Bacino, Carlos A, Battini, Roberta, Bertini, Enrico, Brogan, Paul A, Brueton, Louise A, Carpanelli, Marialuisa, De Laet, Corinne, de Lonlay, Pascale, del Toro, Mireia, Desguerre, Isabelle, Fazzi, Elisa, Garcia-Cazorla, Angels, Heiberg, Arvid, Kawaguchi, Masakazu, Kumar, Ram, Lin, Jean-Pierre S-M, Lourenco, Charles M, Male, Alison M, Marques Jr, Wilson, Mignot, Cyril, Olivieri, Ivana, Orcesi, Simona, Prabhakar, Prab, Rasmussen, Magnhild, Robinson, Robert A, Rozenberg, Flore, Schmidt, Johanna L, Steindl, Katharina, Tan, Tiong Y, van der Merwe, William G, Vanderver, Adeline, Vassallo, Grace, Wakeling, Emma L, Wassmer, Evangeline, Whittaker, Elizabeth, Livingston, John H, Lebon, Pierre, Suzuki, Tamio, McLaughlin, Paul J, Keegan, Liam P, O'Connell, Mary A, Lovell, Simon C, Crow, Yanick J

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An immunogenetic map of Lombardy (Northern Italy) von MARTINETTI, M., DEGIOANNI, A., D'ARONZO, A. M., BENAZZI, E., CARPANELLI, R., CASTELLANI, L., CENZUALES, S., DE BIASE, U., DE FILIPPO, C., DE GIULI, A., GEROSA, A., FARÈ, M., FERRIOLI, G., GALVANI, G., LOMBARDO, C., MALAGOLI, A., MARCHESI, S., MASCARETTI, L., MOTTA, F., SIOLI, V., RINALDINI, C., RIZZOLO, L., PASCUTTO, C., BERNARDINELLI, L., SALVANESCHI, L.

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IDB’s Ninth General Capital Increase: Implementation and Results von Soldano, Miguel, Gonzalez Diez, Verónica M, Haarsager, Ulrike, Hernández, María José, Linares, Ana María, García, Juan Felipe, Szwedzki, Roni, Ahumada, Alejandro, Alejandre, Florencia, Gwin, Catherine, Alonso, Pablo, Schijman, Agustina, Crespo, Anna Risi Vianna, Wattenbach, Horst, Michelitsch, Roland, Putic, Melanie, Khadr, Ali, Puerta, Juan Manuel, Carpanelli, María del Mar, Legarreta, Regina, Huppi, Monika, Florimon, Andrea, Gray, Cheryl, Setien Santianez, Loreto, Elliott, Victoria, Soriano, Alejandro

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