Hidden outpatient oncology Clinical Nursing Minimum Data Set: Findings from an Italian multi-method study von Palese, Alvisa, Zanini, Antonietta, Carlevaris, Erika, Morandin, Annalisa, Carpanelli, Ivana, Dante, Angelo

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Italian oncology nurses' knowledge of complementary and alternative therapies: national survey von Zanini, Antonietta, Quattrin, Rosanna, Goi, Debora, Frassinelli, Barbara, Panariti, Mateo, Carpanelli, Ivana, Brusaferro, Silvio

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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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